EGAS00000000001
WTCCC case-control study for Bipolar Disorder
Other
1980-01-01
EGAS00000000002
WTCCC case-control study for Bipolar Disorder - Combined Controls
Other
1980-01-01
EGAS00000000003
WTCCC case-control study for Coronary Artery Disease
Other
1980-01-01
EGAS00000000004
WTCCC case-control study for Coronary Artery Disease - Combined Controls
Other
1980-01-01
EGAS00000000005
WTCCC case-control study for Coronary Artery Disease, Hypertension, T2D - combined cases
Other
1980-01-01
EGAS00000000006
Genomewide Association Study of Inflammatory Bowel Disease
Other
1980-01-01
EGAS00000000007
Genomewide Association Study of Inflammatory Bowel Disease - Combined Controls
Other
1980-01-01
EGAS00000000008
WTCCC case-control study for Inflammatory Bowel Disease, T1D and RA - combined cases
Other
1980-01-01
EGAS00000000009
WTCCC case-control study for Hypertension
Other
1980-01-01
EGAS00000000010
WTCCC case-control study for Hypertension - Combined Controls
Other
1980-01-01
EGAS00000000011
WTCCC case-control study for Rheumatoid Arthritis
Other
1980-01-01
EGAS00000000012
WTCCC case-control study for Rheumatoid Arthritis - Combined Controls
Other
1980-01-01
EGAS00000000013
WTCCC case-control study for T1D and RA - combined cases
Other
1980-01-01
EGAS00000000014
WTCCC case-control study for Type 1 Diabetes
Other
1980-01-01
EGAS00000000015
WTCCC case-control study for Type 1 Diabetes - Combined Controls
Other
1980-01-01
EGAS00000000016
WTCCC case-control study for Type 2 Diabetes
Other
1980-01-01
EGAS00000000017
WTCCC case-control study for Type 2 Diabetes - Combined Controls
Other
1980-01-01
EGAS00000000018
WTCCC case-control study for Ankylosing Spondylitis
Other
1980-01-01
EGAS00000000019
WTCCC case-control study for Ankylosing Spondylitis - Combined Controls
Other
1980-01-01
EGAS00000000020
WTCCC case-control study for Autoimmune Thyroid Disease
Other
1980-01-01
EGAS00000000021
WTCCC case-control study for Autoimmune Thyroid Disease - Combined Controls
Other
1980-01-01
EGAS00000000022
WTCCC case-control study for Multiple Sclerosis
Other
1980-01-01
EGAS00000000023
WTCCC case-control study for Multiple Sclerosis - Combined controls
Other
1980-01-01
EGAS00000000024
WTCCC case-control study for Breast cancer
Other
1980-01-01
EGAS00000000025
WTCCC case-control study for Breast cancer - Combined Controls
Other
1980-01-01
EGAS00000000026
MalariaGEN case-control study in the Gambia
Other
1980-01-01
EGAS00000000027
WTCCC case-control study for Tuberculosis
Other
1980-01-01
EGAS00000000028
WTCCC2 project controls - 1958 British Birth Cohort and National Blood Service
Other
1980-01-01
EGAS00000000029
Massive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development
Whole Genome Sequencing
1980-01-01
EGAS00000000030
Nordic Samples on build 36
Other
1980-01-01
EGAS00000000031
HLA has strongest association with IgA nephropathy in genome-wide analysis
Other
1980-01-01
EGAS00000000032
Control sets genotyped with Dynal RELI SSO and Roche Molecular Systems platfroms
Other
1980-01-01
EGAS00000000033
Geographical structure and differential natural selection among North European populations
Other
1980-01-01
EGAS00000000034
Genome-wide association scan in Parkinson's disease
Other
1980-01-01
EGAS00000000036
HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans
Other
1980-01-01
EGAS00000000037
Carbamazepine-induced hypersensitivity reactions in Europeans
Other
1980-01-01
EGAS00000000038
T1DGC GWAS 1958 British Birth Cohort controls
Other
1980-01-01
EGAS00000000039
WTCCC3 case-control study for Primary Biliary Cirrhosis
Other
1980-01-01
EGAS00000000040
Mutation of FOXL2 in granulosa cell tumors of the ovary
Whole Genome Sequencing
1980-01-01
EGAS00000000043
WNT-signaling and Dupuytren's Disease
Other
1980-01-01
EGAS00000000048
A MITF germline mutation predisposes to melanoma and renal cell carcinoma
Other
1980-01-01
EGAS00000000051
A small cell lung cancer genome reports complex tobacco exposure signatures
Whole Genome Sequencing
1980-01-01
EGAS00000000052
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Whole Genome Sequencing
1980-01-01
EGAS00000000053
Coeliac Disease Immunochip dataset
Other
1980-01-01
EGAS00000000054
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
Whole Genome Sequencing
1980-01-01
EGAS00000000055
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Other
1980-01-01
EGAS00000000056
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
Other
1980-01-01
EGAS00000000057
Genome wide association study of Coeliac Disease
Other
1980-01-01
EGAS00000000059
Assessment of genomic copy number alterations in breast cancer
Cancer Genomics
1980-01-01
EGAS00000000060
A genome-wide meta analysis on stroke and ischemic stroke within four populations
Other
1980-01-01
EGAS00000000062
Complex Landscapes of Somatic Rearrangements in Human Breast Cancer Genomes
Whole Genome Sequencing
1980-01-01
EGAS00000000064
The patterns and dynamics of genomic instability in metastatic pancreatic cancer
Whole Genome Sequencing
1980-01-01
EGAS00000000074
Evolution of an adenomacarcinoma in response to selection by targeted kinase inhibitors
Other
1980-01-01
EGAS00000000075
ARID1A Mutations in Endometriosis-Associated Ovarian Carcinomas
Other
1980-01-01
EGAS00000000077
A Large-Scale, Consortium-Based Genomewide Association Study of Asthma
Other
1980-01-01
EGAS00000000082
ZNF703 is a common Luminal B breast cancer oncogene that differentially regulates luminal and basal progenitors in human mammary epithelium.
Other
1980-01-01
EGAS00000000083
METABRIC
Other
1980-01-01
EGAS00000000084
WTCCC2 case-control study for Ulcerative Colitis
Other
1980-01-01
EGAS00000000086
An immune response network associated with blood lipid levels
Other
1980-01-01
EGAS00000000087
Genome-wide association study of severe malaria in Gambian mother-father-child trios
Other
1980-01-01
EGAS00000000088
Genome-wide association study of severe malaria in Ghanain mother-farther-child trios
Other
1980-01-01
EGAS00000000092
CLL Genome
Cancer Genomics
1980-01-01
EGAS00000000097
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Other
1980-01-01
EGAS00000000098
METABRIC
Other
1980-01-01
EGAS00000000099
Identification of genetic etiology of CAMRQ2
Other
1980-01-01
EGAS00000000101
The Genetic Analysis of multiple sclerosis
Other
1980-01-01
EGAS00000000102
Molecular Phenotyping to Accelerate Genomic Epidemiology (MolPAGE)
Other
1980-01-01
EGAS00000000103
WTCCC2 Ischaemic Stroke study
Other
1980-01-01
EGAS00000000104
Genomewide association studies in ankylosing spondylitis
Other
1980-01-01
EGAS00000000105
Copy number analysis of Diamond-Blackfan Anemia (DBA) using SNP array
Other
1980-01-01
EGAS00000000108
Genome-wide association scan in psoriasis
Other
1980-01-01
EGAS00000000109
Genetics of gene expression in primary human immune cells
Other
1980-01-01
EGAS00000000114
Krakow experiment - Northern Finland Birth Cohort 1966
Other
1980-01-01
EGAS00000000115
Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Other
1980-01-01
EGAS00000000116
Molecular Sub-grouping of CNS-PNET
Other
1980-01-01
EGAS00000000118
WTCCC2 Schizophrenia study
Other
1980-01-01
EGAS00000000119
Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
Other
1980-01-01
EGAS00000000121
WTCCC2 Pharmacogenomic Response to Statins study
Other
1980-01-01
EGAS00000000122
METABRIC miRNA landscape
Other
1980-01-01
EGAS00000000129
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Other
1980-01-01
EGAS00000000131
Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese Samples
Other
1980-01-01
EGAS00000000132
The Haemgen RBC study
Other
1980-01-01
EGAS00000000134
NOWAC blood-based breast cancer case-control study
Other
1980-01-01
EGAS00000000135
Genome-wide differential DNA methylation signatures in pediatric acute
lymphoblastic leukemia
Other
1980-01-01
EGAS00000000137
MRCA and MRCE SNP genotypes
Other
1980-01-01
EGAS00001000001
Exome Resequencing of Progressive Hearing Loss
Resequencing
2010-09-03
EGAS00001000002
Breast Cancer Follow Up Series
Cancer Genomics
2010-09-08
EGAS00001000003
Cancer Single Cell Sequencing
Other
2010-09-15
EGAS00001000004
Multifocal_Breast_Project
Cancer Genomics
2010-10-13
EGAS00001000005
Lung_Rearrangement_Study
Cancer Genomics
2010-10-15
EGAS00001000006
Renal_Cancer_Exome_Sequencing
Cancer Genomics
2010-10-28
EGAS00001000008
Whole_Genome_Sequencing_of_hiPS_cells
Whole Genome Sequencing
2010-11-04
EGAS00001000009
SCLC
Synthetic Genomics
2010-11-10
EGAS00001000011
CLL_cancer_Sample_Sequencing
Cancer Genomics
2010-11-17
EGAS00001000012
Various_Cancer_Fusion_Gene_Sequencing
Cancer Genomics
2010-11-17
EGAS00001000013
Osteosarcoma_Sequencing
Cancer Genomics
2010-11-17
EGAS00001000014
CLL_Cancer_Whole_Genome_Sequencing
Cancer Genomics
2010-11-17
EGAS00001000016
The_GENCODE_exome___sequencing_the_complete_human_exome
Exome Sequencing
2010-11-17
EGAS00001000017
Familial Melanoma Sequencing
Exome Sequencing
2010-11-26
EGAS00001000020
Genetic_variation_in_Kuusamo
Population Genomics
2011-01-04
EGAS00001000023
Identifying autosomal recessive mutations causing neurological disorders
Other
2011-01-11
EGAS00001000024
Piloting exome resequencing in consanguineous families with homozygosity mapping intervals
Other
2011-01-11
EGAS00001000025
Whole_exome_sequencing_of_Severe_Insulin_Resistant_patients_
Other
2011-01-12
EGAS00001000026
Whole_Exome_Sequencing_for_Characterization_of_Disease_Causing_Mutations_in_two_Pakistani_Families_Suffering_from_Autosomal_Recessive_Ocular_Disorders_
Other
2011-01-12
EGAS00001000027
TMD_AMLK_Exome_Study
Cancer Genomics
2011-01-17
EGAS00001000028
PV_Exome_Study
Cancer Genomics
2011-01-17
EGAS00001000030
ADCC_Rearrangement_Screen
Cancer Genomics
2011-02-02
EGAS00001000031
Matched_breast_cancer_fusion_gene_study
Cancer Genomics
2011-02-07
EGAS00001000032
Kaposi_sarcoma_exome
Cancer Genomics
2011-02-07
EGAS00001000033
1__Fanconi_Anemia_transformation_to_AML
Cancer Genomics
2011-02-14
EGAS00001000034
MDSMPN_Rearrangement_Screen
Cancer Genomics
2011-02-14
EGAS00001000035
Sequencing_Acute_Myeloid_Leukaemia_
Synthetic Genomics
2011-02-18
EGAS00001000036
Integrative_Oncogenomics_of_Multiple_Myeloma
Cancer Genomics
2011-03-01
EGAS00001000037
Gastric_and_Esophageal_tumour_rearrangement_screen
Cancer Genomics
2011-03-03
EGAS00001000038
Chondrosarcoma_Exome_
Cancer Genomics
2011-03-15
EGAS00001000040
Exome sequencing of hyperplastic polyposis patients
Other
2011-03-17
EGAS00001000041
Disorders_of_growth_and_insulin_action_
Other
2011-03-17
EGAS00001000042
HER2_positive_Breast_Cancer_
Cancer Genomics
2011-03-18
EGAS00001000043
Investigating_low_frequency_variants_in_CAD_MI_cases__controls_and_pedigrees_using_whole_exome_sequencing_and_custom_pulldowns
Other
2011-03-22
EGAS00001000044
Identification_and_functional_validation_of_driver_mutations_in_colorectal_cancer
Other
2011-03-23
EGAS00001000046
Mutational_Screening_of_Human_Acute_Myleloid_Leukaemia_Samples
Other
2011-04-01
EGAS00001000047
Whole Exome Sequencing of Permanent Neonatal Diabetes Patients
Other
2011-04-01
EGAS00001000048
Paroxysmal neurological disorders
Other
2011-04-01
EGAS00001000049
Exome_sequencing_in_patients_with_Calcific_Aortic_Valve_Stenosis
Other
2011-04-04
EGAS00001000050
Investigating_low_frequency_variants_in_CAD_MI_cases__controls_and_pedigrees_using_whole_exome_sequencing_and_custom_pulldowns
Other
2011-04-04
EGAS00001000052
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Other
2011-04-05
EGAS00001000053
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Other
2011-04-05
EGAS00001000054
Identifying causative mutations for Thrombocytopenia with Absent Radii
Other
2011-04-05
EGAS00001000055
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Other
2011-04-05
EGAS00001000057
An exome sequencing pilot study of HIV elite-long term non progressors and rapid progressors
Other
2011-04-12
EGAS00001000058
Acute_Lymphoblastic_Leukemia_Sequencing
Cancer Genomics
2011-04-13
EGAS00001000059
De_novo_mutations_in_schizophrenia_
Other
2011-04-14
EGAS00001000060
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Whole Genome Sequencing
2011-04-21
EGAS00001000061
Lethal malformation syndrome
Other
2011-05-04
EGAS00001000062
The_International_1q_type_2_diabetes_consortium
Other
2011-05-06
EGAS00001000063
Exome_sequencing_in_patients_with_cardiac_arrhythmias
Other
2011-05-06
EGAS00001000064
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Other
2011-05-13
EGAS00001000065
Whole_genome_sequencing_of_Crohn_s_disease_patients
Whole Genome Sequencing
2011-05-17
EGAS00001000066
Congenital Heart Disease in UK Families
Other
2011-05-18
EGAS00001000067
Samples from the Greek island of Crete, MANOLIS cohort
Whole Genome Sequencing
2011-05-19
EGAS00001000068
ORCADES_WGA
Whole Genome Sequencing
2011-05-23
EGAS00001000069
Determination of the molecular nature of the Vel blood group by exome sequencing
Other
2011-05-27
EGAS00001000070
Recurrent Somatic Mutations in CLL
Cancer Genomics
2011-06-01
EGAS00001000071
Tetralogy of Fallot Exome Trios
Other
2011-06-08
EGAS00001000074
Screening_for_human_epigenetic_variation_at_CpG_islands
Epigenetics
2011-06-17
EGAS00001000075
Functional_characterisation_of_CpG_islands_in_human_and_mouse_tissues
Epigenetics
2011-06-17
EGAS00001000076
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Epigenetics
2011-06-17
EGAS00001000077
Human_Colorectal_Cancer_Exome_Sequencing
Other
2011-06-23
EGAS00001000078
SFHS_pedigrees
Whole Genome Sequencing
2011-06-23
EGAS00001000079
Cardiogenics_re_sequencing
Resequencing
2011-06-24
EGAS00001000080
CRLF2_sequencing_project_
Cancer Genomics
2011-06-24
EGAS00001000081
CRLF2_sequencing_project_Exomes
Cancer Genomics
2011-06-24
EGAS00001000082
ALK_inhibitors_in_the_context_of_ALK_dependent_cancer_cell_lines
Cancer Genomics
2011-06-24
EGAS00001000083
CAGEKID: Cancer Genomics of the Kidney
Cancer Genomics
2011-06-24
EGAS00001000085
Linking genes, genomic instability and molecular subgroups in medulloblastoma
Whole Genome Sequencing
2011-06-30
EGAS00001000086
Dilgom_Exome
Other
2011-06-30
EGAS00001000087
Burden_of_Disease_in_Sarcoma
Cancer Genomics
2011-07-01
EGAS00001000088
Familial_Thrombocytosis_germline_exome_sequencing
Cancer Genomics
2011-07-05
EGAS00001000089
Myelodysplastic_Syndrome_Exome_Sequnecing
Other
2011-07-05
EGAS00001000090
UK10K COHORT ALSPAC
Other
2011-07-13
EGAS00001000091
Grey_Platelet_Syndrome__GPS_
Other
2011-07-14
EGAS00001000092
Triple_Negative_Breast_Cancer_Whole_Genomes
Cancer Genomics
2011-07-20
EGAS00001000093
Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density
Other
2011-07-21
EGAS00001000094
PREDICT
Cancer Genomics
2011-07-27
EGAS00001000095
Renal_Follow_Up_Series
Cancer Genomics
2011-08-04
EGAS00001000096
Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
Resequencing
2011-08-05
EGAS00001000097
Chromatin_Profiling_in_Twins
Gene Regulation Study
2011-08-09
EGAS00001000098
Chromatin_Profiling_in_Twins
Gene Regulation Study
2011-08-09
EGAS00001000099
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Other
2011-08-11
EGAS00001000100
Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias
Other
2011-08-11
EGAS00001000101
UK10K_RARE_NEUROMUSCULAR
Other
2011-08-16
EGAS00001000102
ET_Exome
Cancer Genomics
2011-08-17
EGAS00001000103
Genomics_of_Colorectal_Cancer_Metastases___Massively_Parallel_Sequencing_of_Matched_Primary_and_Metastatic_tumours_to_Identify_a_Metastatic_Signature_of_Somatic_Mutations__MOSAIC_
Cancer Genomics
2011-08-17
EGAS00001000104
Hyperfibrinolysis
Other
2011-08-17
EGAS00001000105
Platelet_collagen_defect
Other
2011-08-17
EGAS00001000106
Bleeding
Other
2011-08-17
EGAS00001000107
Various_Platelet_Disorders
Other
2011-08-17
EGAS00001000108
UK10K COHORT TWINSUK
Other
2011-08-18
EGAS00001000109
UK10K NEURO ABERDEEN
Other
2011-08-18
EGAS00001000110
UK10K_NEURO_ASD_FI
Exome Sequencing
2011-08-18
EGAS00001000111
UK10K NEURO ASD BIONED
Other
2011-08-18
EGAS00001000112
UK10K NEURO ASD GALLAGHER
Exome Sequencing
2011-08-18
EGAS00001000113
UK10K NEURO ASD MGAS
Other
2011-08-18
EGAS00001000114
UK10K NEURO ASD SKUSE
Other
2011-08-18
EGAS00001000115
UK10K NEURO ASD TAMPERE
Other
2011-08-18
EGAS00001000117
UK10K NEURO EDINBURGH
Other
2011-08-18
EGAS00001000118
UK10K NEURO FSZ
Other
2011-08-18
EGAS00001000119
UK10K NEURO FSZNK
Other
2011-08-18
EGAS00001000120
UK10K NEURO IMGSAC
Other
2011-08-18
EGAS00001000121
UK10K NEURO IOP COLLIER
Other
2011-08-18
EGAS00001000122
UK10K_NEURO_MUIR
Exome Sequencing
2011-08-18
EGAS00001000123
UK10K NEURO UKSCZ
Exome Sequencing
2011-08-18
EGAS00001000124
UK10K_OBESITY_SCOOP
Exome Sequencing
2011-08-18
EGAS00001000125
UK10K RARE CHD
Other
2011-08-18
EGAS00001000126
UK10K_RARE_CILIOPATHIES
Other
2011-08-18
EGAS00001000127
UK10K RARE COLOBOMA
Other
2011-08-18
EGAS00001000128
UK10K_RARE_FIND
Other
2011-08-18
EGAS00001000129
UK10K_RARE_HYPERCHOL
Exome Sequencing
2011-08-18
EGAS00001000130
UK10K_RARE_SIR
Other
2011-08-18
EGAS00001000131
UK10K_RARE_THYROID
Exome Sequencing
2011-08-18
EGAS00001000132
The clonal and mutational evolution spectrum of primary triple negative breast cancers
Exome Sequencing
2011-08-18
EGAS00001000133
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Other
2011-08-22
EGAS00001000134
An_evaluation_of_different_strategies_for_large_scale_pooled_sequencing_study_design_
Resequencing
2011-08-25
EGAS00001000135
Recurrent somatic DICER1 mutations in non-epithelial ovarian tumors
Cancer Genomics
2012-01-04
EGAS00001000136
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Resequencing
2011-09-01
EGAS00001000137
ENGAGE___Amendment__500_genes_exon_sequencing_
Other
2011-09-06
EGAS00001000138
Radiotherapy_induced_sarcoma
Cancer Genomics
2011-09-08
EGAS00001000139
Splenic_Marginal_Zone_Lymphoma_with_villous_lymphocytes_exome_sequencing
Cancer Genomics
2011-09-08
EGAS00001000140
Xenograft_Sequencing
Cancer Genomics
2011-09-09
EGAS00001000142
Exome sequencing of patients with structural brain malformations
Other
2011-09-20
EGAS00001000145
A_study_of_the_genetic_basis_of_evation_by_Acute_Myeloid_Leukaemia_of_Graft_vs_Leukaemia_effects_after_allogeneic_bone_marrow_transplantation
Other
2011-09-21
EGAS00001000146
Exome_Sequencing_of_Poor_Prognosis_Acute_Myeloid_Leukaemia
Other
2011-09-23
EGAS00001000147
Osteosarcoma_Whole_Genome
Cancer Genomics
2011-09-23
EGAS00001000148
Lung_Cancer_Whole_Genomes
Cancer Genomics
2011-09-27
EGAS00001000149
Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency
Exome Sequencing
2011-09-30
EGAS00001000151
Exome_sequencing_Parkinson_s_disease_patients
Other
2011-09-30
EGAS00001000152
Full genome sequencing of a monozygotic twin discordant for schizophrenia
Whole Genome Sequencing
2011-10-03
EGAS00001000153
Exome Sequencing of Gastric Cancer
Exome Sequencing
2011-10-04
EGAS00001000154
Genome Landscape of Primary Pancreatic Ductal Adenocarcinoma
Other
2011-10-07
EGAS00001000155
Matched_Ovarian_Cancer_Sequencing
Cancer Genomics
2011-10-13
EGAS00001000156
Otosclerosis_gene_discovery_
Other
2011-10-19
EGAS00001000157
Hearing_loss_in_adults_from_South_Carolina_
Other
2011-10-19
EGAS00001000158
Complete Genomics paired end sequencing; Ovarian cancer
Whole Genome Sequencing
2011-10-20
EGAS00001000159
Exome sequencing of patients with rare neurological disorders
Other
2011-10-25
EGAS00001000160
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Cancer Genomics
2011-10-25
EGAS00001000161
Triple_Negative_Breast_Cancer_sequencing
Cancer Genomics
2011-10-27
EGAS00001000162
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Whole Genome Sequencing
2011-11-02
EGAS00001000163
Osteosarcoma_Exome_Sequencing
Cancer Genomics
2011-11-02
EGAS00001000164
ESGI___Molecular_diagnosis_for_mitochondrial_disorders_
Other
2011-11-04
EGAS00001000165
Monotherapy_Breast_Cancer
Cancer Genomics
2011-11-14
EGAS00001000166
Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes
Cancer Genomics
2011-11-14
EGAS00001000167
Abnormal_foetal_development_exome_trios
Other
2011-11-15
EGAS00001000169
Whole genome sequencing of matched primary and metastatic acral melanomas
Cancer Genomics
2011-11-29
EGAS00001000170
20_Matched_Pair_Breast_Cancer_Genomes
Cancer Genomics
2011-11-29
EGAS00001000171
Exome_sequencing_of_blastic_plasmacytoid_dendritic_cell_neoplasms
Other
2011-11-30
EGAS00001000172
BRAF_and_MEK_resistant_cell_line_clones
Cancer Genomics
2011-11-30
EGAS00001000173
Testing_the_feasibility_of_genome_scale_sequencing_in_routinely_collected_FFPE_cancer_specimens_versus_matched_fresh_frozen_samples
Cancer Genomics
2011-11-30
EGAS00001000174
Balanced_Ependymoma
Cancer Genomics
2011-11-30
EGAS00001000175
PMF_Exome_Study
Cancer Genomics
2011-11-30
EGAS00001000176
FRCC_Exome_sequencing
Cancer Genomics
2011-11-30
EGAS00001000177
Meningioma_Exome
Cancer Genomics
2011-11-30
EGAS00001000178
Cell_Line_Sub_Clone_Rearrangement_Screen
Cancer Genomics
2011-11-30
EGAS00001000179
Renal_Matched_Pair_Cell_Line_Exome_Sequencing
Cancer Genomics
2011-11-30
EGAS00001000180
Mixed_Leukemia_Rearrangement_Screen
Cancer Genomics
2011-11-30
EGAS00001000181
Chondrosarcoma_Validation_Study
Cancer Genomics
2011-11-30
EGAS00001000182
Signatures of mismatch repair deficiency in cancer genomes
Whole Genome Sequencing
2011-12-05
EGAS00001000185
Exome_sequencing_of_Congenital_Heart_Disease_families_Leuven
Other
2011-12-09
EGAS00001000187
Exome_sequencing_of_Congenital_Heart_Disease_families_Royal_Brompton
Other
2011-12-09
EGAS00001000188
Chordoma_Exome_Sequencing
Cancer Genomics
2011-12-14
EGAS00001000189
Dyslipidemia
Other
2011-12-19
EGAS00001000190
Paroxysmal_Neurological_Disorders_2
Other
2012-01-03
EGAS00001000191
CML_blast_phase_rearrangement_screen
Cancer Genomics
2011-08-26
EGAS00001000192
Somatic Histone H3 Mutations in Diffuse Intrinsic Pontine Gliomas and Non-Brainstem Paediatric Glioblastomas
Whole Genome Sequencing
2012-01-04
EGAS00001000193
ADCC_Exome_Sequencing
Cancer Genomics
2012-01-09
EGAS00001000194
Radiotherapy_induced_Sarcoma_exome
Cancer Genomics
2012-01-09
EGAS00001000195
Breast_Cancer_Somatic_Genetics_Study_
Cancer Genomics
2012-01-10
EGAS00001000196
SCAT_osteosarcoma_sequencing
Cancer Genomics
2012-01-12
EGAS00001000197
ER___HER2___PR__breast_Cancer_genome_sequencing
Cancer Genomics
2012-01-12
EGAS00001000198
Myeloproliferative_Disorder_Sequencing
Cancer Genomics
2012-01-12
EGAS00001000199
Myeloproliferative_Disorder_Sequencing
Cancer Genomics
2012-01-12
EGAS00001000200
Acute_Lymphoblastic_Leukemia_Exome_sequencing_2_
Cancer Genomics
2012-01-12
EGAS00001000201
Acute_Lymphoblastic_Leukemia_Exome_sequencing
Cancer Genomics
2012-01-12
EGAS00001000202
Glioma_cell_lines_rearrangement_screen
Cancer Genomics
2012-01-12
EGAS00001000203
ChIP_sequencing_in_Cancer_Cell_Lines
Cancer Genomics
2012-01-12
EGAS00001000205
Non_Tumour_Renal_Cell_Line_Sequencing
Cancer Genomics
2012-01-12
EGAS00001000206
Cancer_Exome_Resequencing
Cancer Genomics
2012-01-12
EGAS00001000207
Breast_Cancer_Exome_Resequencing
Cancer Genomics
2012-01-12
EGAS00001000208
Cancer_Genome_Libraries_Tests
Whole Genome Sequencing
2012-01-12
EGAS00001000209
Acute_Myeloid_Leukemia_Sequencing
Cancer Genomics
2012-01-12
EGAS00001000210
Breast_Cancer_Whole_Genome_Sequencing
Cancer Genomics
2012-01-13
EGAS00001000211
Breast_Cancer_Exome_Sequencing
Cancer Genomics
2012-01-13
EGAS00001000212
MuTHER_adipose_tissue_small_RNA_expression
Transcriptome Analysis
2012-01-13
EGAS00001000213
Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
Whole Genome Sequencing
2012-01-25
EGAS00001000214
Test_of_PCR_library_method_on_whole_genmoe_samples
Cancer Genomics
2012-01-27
EGAS00001000215
ICGC PedBrain: Deep-sequencing of childhood brain tumors.
Whole Genome Sequencing
2012-01-27
EGAS00001000216
Melanoma_TIL_Study_Exomes
Other
2012-01-31
EGAS00001000217
Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Exome Sequencing
2012-02-01
EGAS00001000218
CML_Discovery_Project
Cancer Genomics
2012-02-01
EGAS00001000220
Identifying_Novel_Fusion_Genes_in_Myeloma
Cancer Genomics
2012-02-03
EGAS00001000222
Whole Genome Sequencing of Neuroblastoma
Whole Genome Sequencing
2012-02-03
EGAS00001000224
Myelodysplastic_Syndrome_Follow_Up_Series
Cancer Genomics
2012-02-06
EGAS00001000225
UK10K NEURO GURLING
Other
2012-02-10
EGAS00001000226
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Cancer Genomics
2012-02-10
EGAS00001000228
Whole_exome_sequencing_of_rare_autoimmune_related_phenotypes
Other
2012-02-13
EGAS00001000229
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Whole Genome Sequencing
2012-02-13
EGAS00001000230
RNAseq_Pulldown_
Other
2012-02-14
EGAS00001000231
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Whole Genome Sequencing
2012-02-15
EGAS00001000233
Pulldown_cytosine_deaminases
Cancer Genomics
2012-02-24
EGAS00001000237
Ethiopia_Genome_Project__high_coverage_
Whole Genome Sequencing
2012-03-01
EGAS00001000238
Ethiopia_Genome_Project__low_coverage_
Whole Genome Sequencing
2012-03-01
EGAS00001000240
Whole_Exome_sequencing_in_a_large_IBD_pedigree
Other
2012-03-01
EGAS00001000242
UK10K_OBESITY_GS
Other
2012-03-01
EGAS00001000243
Integrative_Oncogenomics_of_multiple_myeloma
Other
2012-03-12
EGAS00001000244
Integrative_Oncogenomics_of_multiple_myeloma
Other
2012-03-12
EGAS00001000245
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Cancer Genomics
2012-03-13
EGAS00001000246
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Whole Genome Sequencing
2012-03-14
EGAS00001000249
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01
Other
2012-03-16
EGAS00001000250
Poikiloderma_syndrome_RNAseq
Cancer Genomics
2012-03-16
EGAS00001000251
Melanoma_Til_Study_RNAseq
Cancer Genomics
2012-03-16
EGAS00001000252
Whole_genome_sequencing_of_Italian_genetic_isolates__Friuli_Venezia_Giulia
Whole Genome Sequencing
2012-03-16
EGAS00001000253
Whole genome sequencing of pediatric BCR-ABL1 positive acute lymphoblastic leukemia
Whole Genome Sequencing
2012-03-20
EGAS00001000254
Genetic landscape of pediatric ependymoma
Whole Genome Sequencing
2012-03-20
EGAS00001000255
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Whole Genome Sequencing
2012-03-20
EGAS00001000256
Genetic landscape of pediatric Rhabdomyosarcoma
Other
2012-03-20
EGAS00001000257
Genetic landscape of pediatric Adrenocortical Tumor
Other
2012-03-20
EGAS00001000260
Targeted_Pulldown_Validation_of_mutations_found_in_whole_genome_sequencing
Cancer Genomics
2012-03-22
EGAS00001000261
Transcriptome_Sequencing_of_Cancer_Cell_Lines
Cancer Genomics
2012-03-22
EGAS00001000262
CRUK-ICGC Prostate Cancer Group Study
Other
2012-03-23
EGAS00001000263
Genetic landscape of pediatric Osteosarcoma
Whole Genome Sequencing
2012-03-26
EGAS00001000264
Shwachman_Diamond_syndrome__SDS___Exome_sequencing
Other
2012-03-26
EGAS00001000266
Exome_sequencing_of_patients_with_Ewings_sarcoma_
Other
2012-03-26
EGAS00001000267
RNAseq_of_patients_with_Ewings_sarcoma
Cancer Genomics
2012-03-26
EGAS00001000268
Accurate mutation detection in leukemia by re-sequencing a cancer gene set
Resequencing
2012-03-29
EGAS00001000269
Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Other
2012-03-29
EGAS00001000271
Comparing sequencing of four proto-typical Burkitt lymphomas (BL) with IG-MYC translocation.
Whole Genome Sequencing
2012-04-17
EGAS00001000272
Whole Genome Methylation in CLL
Epigenetics
2012-04-17
EGAS00001000273
Stratifying and Targeting Pediatric Medulloblastoma through Genomics
Other
2012-04-20
EGAS00001000274
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Whole Genome Sequencing
2012-04-23
EGAS00001000275
AML_targeted_resequencing_study
Cancer Genomics
2012-04-25
EGAS00001000276
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Other
2012-04-26
EGAS00001000277
Chondrosarcoma_Targeted_Sequencing_Study
Cancer Genomics
2012-05-01
EGAS00001000278
Osteosarcoma_Targeted_Sequencing_Study
Cancer Genomics
2012-05-02
EGAS00001000280
Chordoma_Targeted_Sequencing_Study
Cancer Genomics
2012-05-02
EGAS00001000282
Meningioma_Targeted_Sequencing_Study
Cancer Genomics
2012-05-02
EGAS00001000283
RNA_Seq_in_Patients_with_Primordial_Dwarfism
Transcriptome Analysis
2012-05-15
EGAS00001000284
BLUEPRINT RNA-seq data for rare cells in the haematopoietic lineages, from adult and cord blood samples.
Transcriptome Analysis
2012-05-29
EGAS00001000285
Validation_of_a_Haloplex_platform_for_targeted_re_sequencing_of_the_exons_of_25_genes
Resequencing
2012-05-30
EGAS00001000286
APCDR AGV Project: WGS of South African Zulu
Other
2012-05-30
EGAS00001000287
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
Exome Sequencing
2012-05-30
EGAS00001000288
Genentech Colon Cancer Screen
Cancer Genomics
2012-05-31
EGAS00001000289
Lung_Plasma_rearrangement_screen
Cancer Genomics
2012-06-08
EGAS00001000290
Myeloproliferative_Disease_Whole_Genomes
Cancer Genomics
2012-06-08
EGAS00001000291
Myelodysplastic_syndrome_whole_genomes
Cancer Genomics
2012-06-08
EGAS00001000292
Molecular_characterization_of_invasive_lobular_carcinoma
Cancer Genomics
2012-06-15
EGAS00001000293
Evaluation_of_size_selection_on_cancer_specific_sequencing_libraries
Cancer Genomics
2012-06-15
EGAS00001000295
Gene_Discovery_in_Age_Related_Hearing_Loss
Other
2012-06-18
EGAS00001000296
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Exome Sequencing
2012-06-18
EGAS00001000297
Feasibility_of_targeted_capture_sequencing_in_routinely_collected_FFPE_cancer_specimens
Cancer Genomics
2012-06-18
EGAS00001000299
Integrative analysis of small cell lung cancer
Other
2012-06-20
EGAS00001000300
Breast_cancer_sequential_sampling_study
Cancer Genomics
2012-06-21
EGAS00001000301
Cancer_Genome_Project_Exome_Sequencing
Other
2012-06-21
EGAS00001000305
P647_Targeted_resequencing_project
Whole Genome Sequencing
2012-06-26
EGAS00001000306
UK10K OBESITY TWINSUK
Other
2012-06-26
EGAS00001000308
Targeted_sequencing_of_candidate_genes_in_calcific_aortic_valve_stenosis
Other
2012-06-27
EGAS00001000310
RNA_sequencing
Other
2012-06-28
EGAS00001000315
Human_Evolution_3
Whole Genome Sequencing
2012-07-10
EGAS00001000317
Exome_sequencing_of_Congenital_Heart_Disease_families_Toronto
Other
2012-07-17
EGAS00001000318
Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer
Exome Sequencing
2012-07-17
EGAS00001000322
De_novo_mutations_in_cell_free_foetal_DNA__cffDNA_
Whole Genome Sequencing
2012-07-19
EGAS00001000323
Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Whole Genome Sequencing
2012-07-19
EGAS00001000326
BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Epigenetics
2012-08-01
EGAS00001000327
BLUEPRINT RNA-seq data for common cells in the haematopoietic lineages, from adult and cord blood samples.
Transcriptome Analysis
2012-08-01
EGAS00001000328
Sequencing and analysis of a South Asian-Indian personal genome
Whole Genome Sequencing
2012-08-08
EGAS00001000329
Identification_of_low_frequency_variants_associated_with_ulcerative_colitis_using_whole_genome_sequencing
Whole Genome Sequencing
2012-08-09
EGAS00001000330
Osteosarcoma_whole_genome_rearrangement_screen
Cancer Genomics
2012-08-09
EGAS00001000332
Helleday_HRAS_Project
Cancer Genomics
2012-08-09
EGAS00001000333
Multiple_Malignancy_Familial_Comparison
Cancer Genomics
2012-08-09
EGAS00001000334
Genentech Small Cell Lung Cancer (SCLC) Screen
Other
2012-08-09
EGAS00001000335
A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma
Other
2012-08-10
EGAS00001000336
Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Other
2012-08-13
EGAS00001000337
Inferring tumor genomes from peripheral blood i.e. CTCs and plasma-DNA using deep sequencing and targeted enrichment
Cancer Genomics
2012-08-14
EGAS00001000343
Pancreatic Cancer Sequencing Initiative
Exome Sequencing
2012-08-22
EGAS00001000344
Exome_sequencing_of_thyroid_disease_in_Val_Borbera
Other
2012-08-23
EGAS00001000346
Genetic landscape of pediatric Retinoblastoma
Whole Genome Sequencing
2012-08-24
EGAS00001000347
Genetic landscape of pediatric Medulloblastoma
Whole Genome Sequencing
2012-08-24
EGAS00001000348
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Whole Genome Sequencing
2012-08-24
EGAS00001000349
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Other
2012-08-24
EGAS00001000351
BLUEPRINT DNase accessibility (NCMLS)
Epigenetics
2012-08-28
EGAS00001000352
Epilepsy_related_sudden_death
Other
2012-08-29
EGAS00001000353
The_genomic_architecture_of_mesothelioma_
Cancer Genomics
2012-08-31
EGAS00001000354
Primary_Lung_Cancer_whole_genome_study
Cancer Genomics
2012-08-31
EGAS00001000356
Exome_sequencing_of_Bilateral_Anophthalmia_cases__Pilot_Study_
Other
2012-09-04
EGAS00001000358
Sequencing_the_exome_of_12_early_sporadic_human_colorectal_cancers__CRC_
Other
2012-09-05
EGAS00001000359
Mutation_analysis_in_human_iPS_cells_
Resequencing
2012-09-05
EGAS00001000360
Balanced_Brain_Tumour_Whole_Genome_Sequencing
Cancer Genomics
2012-09-07
EGAS00001000362
Ewings_Sarcoma_Rearrangement_Screen
Cancer Genomics
2012-09-07
EGAS00001000363
APCDR AGV Project: WGS of an Ugandan population
Other
2012-09-13
EGAS00001000367
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA
Other
2012-10-02
EGAS00001000368
Exome_sequencing_of_Congenital_Heart_Disease_families_from_the_Competence_Network_Berlin
Other
2012-10-05
EGAS00001000369
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Other
2012-10-08
EGAS00001000370
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Cancer Genomics
2012-10-08
EGAS00001000371
Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia
Exome Sequencing
2012-10-09
EGAS00001000373
Deep_sequencing_analysis_of_human_iPSC_specific_SNVs_in_donor_cell_population
Resequencing
2012-10-11
EGAS00001000374
Deep RNA sequencing in CLL
Other
2012-10-11
EGAS00001000377
Triple_Negative_Breast_Cancer_RNA_Sequencing
Cancer Genomics
2012-10-18
EGAS00001000379
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Whole Genome Sequencing
2012-10-19
EGAS00001000380
GEenetic landscape of hypodiploid acute lymphoblastic leukemia
Whole Genome Sequencing
2012-10-19
EGAS00001000381
Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project
Whole Genome Sequencing
2012-10-22
EGAS00001000382
Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons
Transcriptome Analysis
2012-10-23
EGAS00001000383
The genomic landscape of large and small tumors in early-onset prostate cancer patients
Cancer Genomics
2012-10-24
EGAS00001000384
Oulu_Dyslipidemia_families
Other
2012-10-25
EGAS00001000385
Crohn_s_Exome_Sequencing
Other
2012-10-25
EGAS00001000386
Paroxysmal_neurological_Disorders
Other
2012-10-29
EGAS00001000387
Susceptibility_genes_for_the_development_of_SLE_during_treatment_of_IBD
Other
2012-10-29
EGAS00001000388
Whole_exome_sequencing_of_young_onset_Primary_Sclerosing_Cholangitis
Other
2012-10-29
EGAS00001000389
Whole exome sequencing of virus-associated HCC
Exome Sequencing
2012-10-31
EGAS00001000390
Targeted_gene_fusion_sequencing__Fus_seq__in_mesothelioma
Cancer Genomics
2012-10-31
EGAS00001000392
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Whole Genome Sequencing
2012-11-01
EGAS00001000393
Whole-genome-Sequencing of adult medulloblastoma
Whole Genome Sequencing
2012-11-07
EGAS00001000394
Genome-wide mutation analysis of germinal-center B-cell derived lymphomas within the ICGC MMML-Seq Consortium
Other
2012-11-08
EGAS00001000395
Pancreatic Cancer Sequencing Initiative OICR
Cancer Genomics
2012-11-19
EGAS00001000397
Genome Landscape of High-Grade Serous Ovarian Cancer
Other
2012-11-27
EGAS00001000398
High_powered_complex_trait_association_mapping_through_whole_genome_sequencing_of_a_selected_subpopulation_of_the_INGI_Val_Borbera_genetic_isolate
Whole Genome Sequencing
2012-11-30
EGAS00001000399
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Whole Genome Sequencing
2012-12-02
EGAS00001000400
Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer
Other
2012-12-04
EGAS00001000402
Feasibility_of_targeted_capture_sequencing_in_FFPE_cancer_specimens_2
Cancer Genomics
2012-12-06
EGAS00001000403
BASIS_Genome_Validation_Study
Cancer Genomics
2012-12-14
EGAS00001000404
Myeloproliferative_Neoplasms__MPN__Exome_Validation_Study
Cancer Genomics
2012-12-14
EGAS00001000405
Angiosarcoma_follow_up_study
Cancer Genomics
2012-12-14
EGAS00001000406
Myeloproliferative_Neoplasms__MPN__Targeted_Gene_Screen
Cancer Genomics
2012-12-14
EGAS00001000407
Characterization_of_individual_foci_of_multicentric_multifocal_breast_cancer_using_targeted_next_generation_sequencing
Cancer Genomics
2012-12-14
EGAS00001000408
Targeted_sequencing_of_genes_recurrently_mutated_in_AML
Cancer Genomics
2012-12-14
EGAS00001000409
Chordoma_Sequencing_Project_Whole_Genome
Cancer Genomics
2012-12-14
EGAS00001000410
Chordoma_Sequencing_Project_RNAseq
Cancer Genomics
2012-12-14
EGAS00001000411
The Cardiogenics study
Transcriptome Analysis
2013-01-07
EGAS00001000413
The_Transcriptome_of_PLX4032_resistance
Transcriptome Analysis
2013-01-15
EGAS00001000415
Analysis_of_resistance_to_PLX4032
Other
2013-01-17
EGAS00001000416
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Other
2013-01-21
EGAS00001000417
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Other
2013-01-21
EGAS00001000418
BLUEPRINT Bisulfite-seq (CNAG)
Epigenetics
2013-01-22
EGAS00001000419
Ewings_Sarcoma_RNA_seq_drug_sensitivity
Cancer Genomics
2013-01-28
EGAS00001000420
Breast_Cancer_FRT_RNA_seq
Cancer Genomics
2013-01-28
EGAS00001000421
Paroxysmal_Neurological_Disorders___rare_epilepsies
Other
2013-01-30
EGAS00001000423
Validation_of_Exome_sequencing_of_S7RE_iPSC_lines
Resequencing
2013-02-01
EGAS00001000425
Congenital_Heart_Disease___Pilot
Other
2013-02-04
EGAS00001000426
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Cancer Genomics
2013-02-05
EGAS00001000427
Prostate_Cancer_Whole_Genome_Validations
Cancer Genomics
2013-02-05
EGAS00001000428
Neoadjuvant_Breast_Cancer_Validations
Cancer Genomics
2013-02-05
EGAS00001000429
Whole_genome_sequence_of__third_generation_family_member__SFHS_
Whole Genome Sequencing
2013-02-06
EGAS00001000430
Validation_of_AML_Mutational_Screening
Resequencing
2013-02-13
EGAS00001000433
ICGC_Benchmarking_Exercise
Whole Genome Sequencing
2013-02-15
EGAS00001000434
Matched_Pair_Cell_Line_Tumour_RNAseq
Cancer Genomics
2013-02-15
EGAS00001000435
Single_Cell_Targeted_Sequence_Capture
Cancer Genomics
2013-02-15
EGAS00001000436
Lung_Multi_site_Targeted_Sequence_Capture
Cancer Genomics
2013-02-15
EGAS00001000437
Deep_sequencing_of_S7EPC_genome
Resequencing
2013-02-18
EGAS00001000439
Noninvasive prenatal molecular karyotyping from maternal plasma
Resequencing
2013-02-22
EGAS00001000441
Subclonal_analysis_in_S7RE2_and_S7RE14_iPS_cells
Resequencing
2013-02-25
EGAS00001000442
Cell-type, allelic and genetic signatures in the human pancreatic beta cell transcriptome
Transcriptome Analysis
2013-02-27
EGAS00001000443
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Other
2013-02-28
EGAS00001000446
Passive and active DNA methylation and the interplay with genetic variation in gene regulation
Population Genomics
2013-03-07
EGAS00001000447
Germline Aberrations of PAX5 Cause Susceptibility to pre-B cell Acute Lymphoblastic Leukemia
Exome Sequencing
2013-03-11
EGAS00001000449
The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes
Epigenetics
2013-03-12
EGAS00001000451
Plasma-Seq of patients with metastatic prostate cancer
Other
2013-03-13
EGAS00001000453
Identification of mutations and structural rearrangements in plasma DNA form metastatic prostate cancer patients
Resequencing
2013-03-13
EGAS00001000455
Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years.
Epigenetics
2013-03-15
EGAS00001000458
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Whole Genome Sequencing
2013-03-20
EGAS00001000460
Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Whole Genome Sequencing
2013-03-20
EGAS00001000462
Autozygosity_pilot_Born_in_Bradford
Other
2013-03-21
EGAS00001000464
Validation_of_SNVs_found_by_Exome_seq_in_S2_SF1___SF5_and__SF9_hiPSCs
Resequencing
2013-03-25
EGAS00001000466
FFPE_CPA_Accreditation_Study
Cancer Genomics
2013-03-26
EGAS00001000468
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Cancer Genomics
2013-03-26
EGAS00001000470
CMF_RNA_sequencing
Cancer Genomics
2013-03-26
EGAS00001000472
Whole genome sequencing, SNP array and RNA-seq of uveal melanomas
Other
2013-03-27
EGAS00001000474
Whole genome sequencing and whole exome sequencing of mucosal melanoma
Other
2013-03-27
EGAS00001000476
Negligible impact on missing heritability of autoimmune-locus rare coding-region variants
Resequencing
2013-04-04
EGAS00001000478
Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease
Other
2013-04-05
EGAS00001000480
Egypt_Genome_Project___low_coverage_whole_genome_sequencing
Whole Genome Sequencing
2013-04-09
EGAS00001000482
Egypt_Genome_Project___high_coverage_whole_genome_sequencing
Whole Genome Sequencing
2013-04-09
EGAS00001000484
Whole genome and transcriptome analysis of a sporadic and recurring parathyroid carcinoma
Whole Genome Sequencing
2013-04-09
EGAS00001000486
Whole genome sequencing of acral melanomas
Other
2013-04-12
EGAS00001000488
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Other
2013-04-17
EGAS00001000490
Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Epigenetics
2013-04-22
EGAS00001000492
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Other
2013-04-23
EGAS00001000495
RNA Editing in breast cancer
Transcriptome Analysis
2013-04-23
EGAS00001000501
Bone_Cancer___Rare_Types_Whole_Genome
Cancer Genomics
2013-05-01
EGAS00001000505
Whole genome sequencing of chondrosarcoma
Whole Genome Sequencing
2013-05-08
EGAS00001000506
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Other
2013-05-08
EGAS00001000509
an integrated molecular study of clear cell renal cell carcinoma (ccRCC) including whole-genome/exome and RNA sequencing as well as array-based gene expression/copy-number/methylation analyses
Cancer Genomics
2013-05-13
EGAS00001000510
Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
Whole Genome Sequencing
2013-05-13
EGAS00001000511
Autozygosity_pilot___Pakistani_from_Birmingham
Cancer Genomics
2013-05-15
EGAS00001000513
COLORS_in_IBD__Whole_exome_sequencing_of_early_onset_IBD_patients
Other
2013-05-20
EGAS00001000514
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Whole Genome Sequencing
2013-05-20
EGAS00001000515
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis
Cancer Genomics
2013-05-22
EGAS00001000518
Angiosarcoma_follow_up_2_validation_study
Cancer Genomics
2013-05-24
EGAS00001000520
Cloning_of_the_breakpoint_of_a_novel_translocation_associated_with_T_acute_lymphoblastic_leukaemia
Cancer Genomics
2013-05-24
EGAS00001000521
Whole exome and whole genome sequencing of juvenile myelomonocytic leukemia (JMML)
Other
2013-05-24
EGAS00001000522
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Other
2013-05-28
EGAS00001000523
ESGI_Identification_of_novel_genes_and_mechanisms_leading_to_Primary_Ciliary_Dyskinesia
Other
2013-05-28
EGAS00001000525
Analysis_of_somatic_mutations_in_normal_blood__AML_and_MDS_samples
Other
2013-05-31
EGAS00001000526
Integrative sequencing reveals alterations in untreated and castration resistant prostate cancer
Other
2013-06-03
EGAS00001000528
Tagmentation-based Whole Genome Bisulfite Sequencing
Other
2013-06-05
EGAS00001000530
Whole_exome_sequencing_of_inflammatory_bowel_disease_cases
Other
2013-06-10
EGAS00001000531
Exome_sequence_of_probands_in_Barrett_s_oesophagus_families
Other
2013-06-10
EGAS00001000532
Chromosome Y Philogeny in Sardinia
Other
2013-06-10
EGAS00001000533
Chondromyxoid_fibroma
Cancer Genomics
2013-06-11
EGAS00001000534
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Other
2013-06-12
EGAS00001000536
Identification of point mutations, expression perturbations, and gene fusions in T-cell acute lymphoblastic leukemia by RNA-seq
Other
2013-06-14
EGAS00001000544
Consanguineous_families_with_CHD_KAIMRC
Other
2013-06-17
EGAS00001000545
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Other
2013-06-20
EGAS00001000546
Landscape of gene mutations in Down syndrome-related myeloid disorders
Other
2013-06-25
EGAS00001000547
Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling
Other
2013-06-25
EGAS00001000549
CPC-GENE Prostate Cancer Heterogeneity Study
Other
2013-06-26
EGAS00001000551
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Other
2013-07-02
EGAS00001000552
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Other
2013-07-03
EGAS00001000554
Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma
Other
2013-07-06
EGAS00001000557
Whole exome sequencing of peripheral T-cell lymphoma (PTCL)
Other
2013-07-10
EGAS00001000558
DNA from colon cancer samples and matched normal samples was hybridized on Human 660W-Quad SNP arrays and sequenced in Illumina HiScanSQ.
Other
2013-07-11
EGAS00001000559
ICGC Oesophageal adenocarcinoma - pilot samples
Other
2013-07-19
EGAS00001000561
ICGC PedBrain DNA methylation sequencing
Other
2013-07-24
EGAS00001000562
Whole_genome_sequencing_of_a_Grem1_mutant_human_tumour
Whole Genome Sequencing
2013-07-25
EGAS00001000563
Comparison_of_transcriptional_response_of_induced_pluripotent_stem__iPS__cell_derived_and_monocyte_derived_macrophages_to_bacterial_lipopolysaccharide_stimulation
Transcriptome Analysis
2013-07-25
EGAS00001000564
Lymphocyte_RNA_profiling
Transcriptome Analysis
2013-07-26
EGAS00001000565
Hypermutation of the inactive X chromosome is a frequent event in cancer
Other
2013-07-26
EGAS00001000566
Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing
Other
2013-07-28
EGAS00001000567
Autozygosity_pilot___British_Pakistani_from_Birmingham_2
Other
2013-07-30
EGAS00001000568
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Other
2013-07-31
EGAS00001000569
TMD_AMKL_targeted_follow_up
Cancer Genomics
2013-07-31
EGAS00001000570
Targeted_sequencing_of_genes_recurrently_mutated_in_AML___part2
Cancer Genomics
2013-07-31
EGAS00001000571
POT1_splice_site_mutant_analysis
Transcriptome Analysis
2013-08-01
EGAS00001000572
Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas
Other
2013-08-01
EGAS00001000574
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Other
2013-08-07
EGAS00001000575
Whole genome sequencing and whole exome sequencing of DIPG tumors and matched normal tissue
Other
2013-08-08
EGAS00001000578
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M-mutant pediatric high-grade gliomas
Other
2013-09-11
EGAS00001000579
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Exome Sequencing
2013-09-13
EGAS00001000580
Whole genome sequencing of metastatic melanomas from a patient with primary resistance to BRAF inhibition
Other
2013-09-17
EGAS00001000582
Resistance to anti-EGFR therapy in colorectal cancer
Other
2013-09-20
EGAS00001000584
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Other
2013-09-24
EGAS00001000585
Assessment of genomic copy number alterations in breast cancer
Other
2013-09-25
EGAS00001000586
Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Gene Regulation Study
2013-09-25
EGAS00001000587
Epi_Tax_targeted_sequencing
Cancer Genomics
2013-09-26
EGAS00001000588
Angiosarcoma_whole_exome
Cancer Genomics
2013-09-26
EGAS00001000589
Angiosarcoma_targeted_pulldown_cancer_gene_panel
Cancer Genomics
2013-09-26
EGAS00001000590
Angiosarcoma_RNA_sequencing
Cancer Genomics
2013-09-26
EGAS00001000591
Sequencing_of_rare_human_histiocytic_tumour
Cancer Genomics
2013-09-26
EGAS00001000592
HipSci-Whole Exome sequencing-healthy volunteers
Other
2013-09-30
EGAS00001000593
HipSci-RNAseq-healthy volunteers
Transcriptome Analysis
2013-10-02
EGAS00001000596
Breast_Cancer_Sequential_Sampling_Targeted_Capture
Cancer Genomics
2013-10-11
EGAS00001000597
HKU Gastric Cancer Genomics study - WGS, DNA genotyping array, expression and methylation profiling
Other
2013-10-12
EGAS00001000598
RB1 Gene Inactivation by Chromothripsis in Human Retinoblastoma
Other
2013-10-14
EGAS00001000599
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Other
2013-10-14
EGAS00001000600
Measuring the level of relatedness between NGS datasets
Other
2013-10-15
EGAS00001000602
Whole_exome_sequencing_for_HELIC
Other
2013-10-16
EGAS00001000603
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis_PART2
Cancer Genomics
2013-10-16
EGAS00001000604
These are from Korean HCC samples with exome sequencing
Other
2013-10-17
EGAS00001000605
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Other
2013-10-17
EGAS00001000606
Pseudogene_RNAseq
Cancer Genomics
2013-10-17
EGAS00001000607
SHH medulloblastoma samples
Other
2013-10-21
EGAS00001000610
RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Other
2013-10-22
EGAS00001000612
PLCRC_study
Cancer Genomics
2013-10-24
EGAS00001000613
Mosaic_Colorectal_Metastasis
Cancer Genomics
2013-10-24
EGAS00001000615
Osteosarcoma_RNAseq
Cancer Genomics
2013-10-24
EGAS00001000616
BIG_MS_Pilot
Cancer Genomics
2013-10-24
EGAS00001000617
Identification_of_drug_resistance_genes_in_melanoma
Other
2013-10-28
EGAS00001000619
Acquisition_of_additional_mutations_drives_accelerated_progression_of_NPM1_positive_CMML_to_AML_
Resequencing
2013-10-31
EGAS00001000620
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Other
2013-10-31
EGAS00001000621
Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Other
2013-11-01
EGAS00001000622
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Other
2013-11-05
EGAS00001000624
WTCCC2 project Glaucoma (GL) samples
Other
2013-11-06
EGAS00001000625
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Other
2013-11-12
EGAS00001000626
Haemoglobin_E_beta_thalassaemia_in_a_patient_group_from_Sri_Lanka
Other
2013-11-12
EGAS00001000627
Leiden_melanomafamilies
Whole Genome Sequencing
2013-11-13
EGAS00001000628
WTCCC2 BO (Barretts oesophagus) samples
Other
2013-11-15
EGAS00001000630
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Other
2013-11-22
EGAS00001000641
Mutational context and diverse clonal development in early and late bladder cancer
Other
2013-11-26
EGAS00001000642
Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Other
2013-11-27
EGAS00001000643
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Other
2013-11-27
EGAS00001000644
Genome of the Netherlands
Other
2013-11-28
EGAS00001000646
The study provides comprehensive access to the set of EGA studies which may be useful as controls.
Other
2013-12-06
EGAS00001000647
A Genomics-Based Classification of Human Lung Tumors
Other
2013-12-10
EGAS00001000648
FinHer_Breast_Cancer_Study
Cancer Genomics
2013-12-11
EGAS00001000649
GEL_WGS_Comparison
Cancer Genomics
2013-12-11
EGAS00001000650
Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Other
2013-12-12
EGAS00001000651
Mutational_Signatures_of_relapse_in_rectal_cancer_FFPE_samples_in_the_CR07_clinical_trial
Cancer Genomics
2013-12-13
EGAS00001000652
Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Other
2013-12-13
EGAS00001000653
CD74-NRG1 fusions in lung adenocarcinoma
Other
2013-12-17
EGAS00001000654
PCGP Ph-like ALL
Other
2013-12-17
EGAS00001000655
Combination_therapies_for_personalized_cancer_medicine
Cancer Genomics
2013-12-17
EGAS00001000658
Illumina Human Exome (ExomeChip) genotype data from the Pomak villages in Greece (HELIC Pomak Isolate). 1040 samples all >=16 years old.
Other
2013-12-19
EGAS00001000659
Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data
Other
2013-12-23
EGAS00001000660
High number of somatic mutations found in the healthy blood compartment of a 115-year-old woman reveals oligoclonal hematopoiesis
Other
2013-12-24
EGAS00001000661
Whole-exome analysis of corticotropin-independent Cushing's syndrome
Other
2013-12-26
EGAS00001000662
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Other
2014-01-09
EGAS00001000663
MPN_mutation_order_followup
Cancer Genomics
2014-01-09
EGAS00001000664
Whole-Genome Sequencing of 128 Ashkenazi Jewish individuals
Other
2014-01-09
EGAS00001000665
Integrated genomic characterization of adrenocortical carcinoma
Other
2014-01-13
EGAS00001000667
Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Other
2014-01-14
EGAS00001000668
Study on the consequences of prenatal famine exposure on DNA methylation.
Other
2014-01-15
EGAS00001000669
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Other
2014-01-20
EGAS00001000671
Whole genome sequencing of Japanese HCCs
Other
2014-01-21
EGAS00001000672
WTCCC2 People of the British Isles (POBI) genotypes
Other
2014-01-21
EGAS00001000673
Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Other
2014-01-21
EGAS00001000674
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Other
2014-01-21
EGAS00001000677
Whole exome sequencing of 103 pairs BLCA-CN
Other
2014-01-22
EGAS00001000678
WGS of liver cancer in the Japanese population
Other
2014-01-23
EGAS00001000679
Integrative genomic profiling of hepatocellular adenomas reveals recurrent FRK activating mutations and mutational processes of malignant transformation
Other
2014-01-24
EGAS00001000680
Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing
Other
2014-01-24
EGAS00001000682
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Other
2014-01-27
EGAS00001000685
Recurrent epimutations activate gene body promoters in primary glioblastoma
Other
2014-01-28
EGAS00001000687
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Other
2014-01-29
EGAS00001000689
BLUEPRINT EpiVar Whole Genome Sequencing
Other
2014-01-30
EGAS00001000691
miRNA_expression_in_response_to_LPS_stimulus_in_macrophages
Transcriptome Analysis
2014-02-05
EGAS00001000692
FFPE_CPA_Accreditation_Study__Part_2
Cancer Genomics
2014-02-05
EGAS00001000698
Neuromics / RD-Connect - Huntington's disease
Other
2014-02-06
EGAS00001000703
MDS_Sequential_Treatment_Validation
Cancer Genomics
2014-02-07
EGAS00001000704
Metastatic_breast_cancer_targeted_gene_screen
Cancer Genomics
2014-02-07
EGAS00001000706
Whole-Genome sequencing of hepatocellular carcinomas
Other
2014-02-18
EGAS00001000707
BASIS_RNAseq
Cancer Genomics
2014-02-18
EGAS00001000708
Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors
Other
2014-02-19
EGAS00001000709
whole-genome sequencing in 17 ESCC cases and whole-exome sequencing in 71 cases
Other
2014-02-20
EGAS00001000711
Identification_of_cardiovascular_biomarkers_through_an_integrative_omics_approach
Transcriptome Analysis
2014-02-25
EGAS00001000712
Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Other
2014-02-26
EGAS00001000713
UK10K COHORT IMPUTATION
Other
2014-02-26
EGAS00001000714
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Other
2014-02-28
EGAS00001000716
Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit.
Other
2014-02-28
EGAS00001000717
Autozygosity_pilot___QMUL
Other
2014-03-05
EGAS00001000718
Human_Evolution_3B
Whole Genome Sequencing
2014-03-05
EGAS00001000719
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Other
2014-03-06
EGAS00001000720
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Other
2014-03-06
EGAS00001000721
Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Other
2014-03-06
EGAS00001000722
UQCCR/QCMG brain metastasis sequence analysis
Other
2014-03-07
EGAS00001000723
ICGC Oesophageal adenocarcinoma - normal samples
Other
2014-03-07
EGAS00001000724
ICGC Oesophageal adenocarcinoma - 100 tumour samples
Other
2014-03-07
EGAS00001000725
ICGC Oesophageal adenocarcinoma - tumour samples
Other
2014-03-07
EGAS00001000726
ICGC Oesophageal adenocarcinoma - Barrett's samples
Other
2014-03-07
EGAS00001000727
ICGC Oesophageal adenocarcinoma - lymph-node samples
Other
2014-03-07
EGAS00001000728
SPECTA__NGS_Screening_Program_for_Efficient_Clinical_Trial_Access
Cancer Genomics
2014-03-07
EGAS00001000729
Whole Exome Sequencing of cohorts of Mutant Braf mouse model melanoma DNA and germline DNA.
Other
2014-03-10
EGAS00001000730
Metastatic_Prostate_Follow_Up
Cancer Genomics
2014-03-14
EGAS00001000731
Plasma RNA sequencing
Other
2014-03-14
EGAS00001000732
TMD_AMKL_targeted_follow_up_part_2
Cancer Genomics
2014-03-14
EGAS00001000733
Barcelona_kids_with_melanoma
Whole Genome Sequencing
2014-03-17
EGAS00001000734
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Other
2014-03-18
EGAS00001000736
Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Other
2014-03-18
EGAS00001000737
Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Other
2014-03-19
EGAS00001000738
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Other
2014-03-20
EGAS00001000740
DNA_repair_in_BLM_deficient_hiPSCs
Other
2014-03-20
EGAS00001000741
Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Epigenetics
2014-03-20
EGAS00001000742
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Transcriptome Analysis
2014-03-20
EGAS00001000743
Myeloma_Follow_up_Pilot
Cancer Genomics
2014-03-20
EGAS00001000744
ICGC medulloblastoma whole genome sequencing data, ICGC release 16
Other
2014-03-21
EGAS00001000747
ESGI_Exome_sequencing_in_Circulating_Tumor_Cells_to_determine_therapy_related_markers_____
Other
2014-03-26
EGAS00001000749
Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency
Other
2014-03-27
EGAS00001000750
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Other
2014-03-28
EGAS00001000751
Transposome_Bisulfite_Sequencing
Cancer Genomics
2014-03-28
EGAS00001000752
BLUEPRINT EpiVar RNA-seq for Naive naive CD4+ T-cells
Other
2014-03-28
EGAS00001000753
BLUEPRINT EpiVar ChIP-seq for naive CD4+ T-cells
Other
2014-03-28
EGAS00001000756
Metastatic_Prostate_Follow_Up_2
Cancer Genomics
2014-03-31
EGAS00001000758
TCELL_PILOT_ATAC_SEQ
Transcriptome Analysis
2014-04-02
EGAS00001000760
Unraveling metastatic progression of breast cancer
Other
2014-04-03
EGAS00001000761
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Other
2014-04-03
EGAS00001000762
Genetics_and_Networks_of_Congenital_Heart_Defects
Other
2014-04-07
EGAS00001000763
Expressed_fusion_transcripts_in_rare_bone_tumours
Cancer Genomics
2014-04-08
EGAS00001000764
SINGLE_CELL_ANALYSIS_OF_IN_VITRO_ERYTHROPOIESIS
Transcriptome Analysis
2014-04-10
EGAS00001000765
MPN_TGS2_Follow_up___PT1_Vori_other
Cancer Genomics
2014-04-10
EGAS00001000767
Next generation sequencing of sporadic schwannomatosis samples
Other
2014-04-11
EGAS00001000768
Low_Coverage_Sequencing_of_rare_human_histiocytic_tumour
Cancer Genomics
2014-04-14
EGAS00001000769
Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected
Other
2014-04-15
EGAS00001000772
MYD88/TLR mutations in CLL
Other
2014-04-22
EGAS00001000773
WTCCC2 Visceral Leishmaniasis (VL) samples
Other
2014-04-24
EGAS00001000775
Deciphering Developmental Disorders (DDD)
Other
2014-04-28
EGAS00001000789
Moles
Cancer Genomics
2014-04-30
EGAS00001000790
Exploration_of__mutational_processes_in_human_cancer_cell_lines__Exome
Cancer Genomics
2014-04-30
EGAS00001000793
Two lung cancer cell lines with EGFR mutations, PC-9 and KHM-3S, were either treated with Tarceva for 24 hours or left untreated. The gene expression profiles were examined by RNAseq, and the genome wide binding profiles of total STAT3 and pSTAT3 were characterized by ChIPseq.
Other
2014-04-30
EGAS00001000800
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Whole Genome Sequencing
2014-05-06
EGAS00001000801
TBA
Whole Genome Sequencing
2014-05-06
EGAS00001000802
TBA
Whole Genome Sequencing
2014-05-06
EGAS00001000803
TBA
Whole Genome Sequencing
2014-05-06
EGAS00001000805
RNA-seq data from the EUROBATS Project in four tissues: Fat, LCL, Skin and whole Blood.
Other
2014-05-06
EGAS00001000807
Imputation-Based Meta-Analysis of Severe Malaria in Three African Populations
Other
2014-05-08
EGAS00001000808
Whole_exome_sequencing_CHD_trios
Other
2014-05-08
EGAS00001000809
TRACERx: TRAcking non-small cell lung Cancer Evolution through therapy (Rx). Pilot Study. Multi-region sequencing of early-stage NSCLCs.
Other
2014-05-08
EGAS00001000812
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Cancer Genomics
2014-05-09
EGAS00001000813
RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Cancer Genomics
2014-05-09
EGAS00001000814
Study_to_investigate_the_prevalence__of_leukaemic_mutations_in_whole_blood_DNA_in_a_cohort_of_blood_donors
Resequencing
2014-05-09
EGAS00001000815
Identification_of_drug_resistance_genes_in_melanoma_by_mRNA_gene_expression
Transcriptome Analysis
2014-05-13
EGAS00001000816
Identification_of_drug_resistance_genes_in_melanoma_by_small_RNAs_expression_analysis
Transcriptome Analysis
2014-05-13
EGAS00001000817
A WTCCC2 genome-wide association study for psychosis endophenotype (PE) in individuals from UK, Germany, Holland, Spain and Australia.
Other
2014-05-13
EGAS00001000824
Diverse modes of genomic alterations in hepatocellular carcinoma
Other
2014-05-15
EGAS00001000825
Whole_Exome_Sequencing_of_INTERVAL
Other
2014-05-19
EGAS00001000826
Reproducibility of variant calls in replicate next generation sequencing experiments
Other
2014-05-19
EGAS00001000828
CGP_CORE_CELL_LINES___RNA_seq
Cancer Genomics
2014-05-22
EGAS00001000830
Mesothelioma_Whole_Genomes
Cancer Genomics
2014-05-22
EGAS00001000836
FFPE_Normal_Panel_V3_Cancer_Panel
Cancer Genomics
2014-05-30
EGAS00001000837
Lung_Progression_versus_Regression_Whole_Genome_Sequencing
Cancer Genomics
2014-05-30
EGAS00001000839
Targeting the DNA Repair Pathway in Ewing Sarcoma
Other
2014-06-02
EGAS00001000840
Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution.
Other
2014-06-03
EGAS00001000841
HumanMethylation450K data from Purified Plasma Cells of Monoclonal gammopathy of unknown significance and Multiple myeloma patients and Healthy donors
Other
2014-06-03
EGAS00001000845
Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Other
2014-06-03
EGAS00001000849
Celiac disease case-control North Indian Immunochip dataset
Other
2014-06-04
EGAS00001000850
Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing
Whole Genome Sequencing
2014-06-04
EGAS00001000851
Primary_angiosarcoma_Whole_Genome_Sequencing
Cancer Genomics
2014-06-05
EGAS00001000852
Benchmark and validation of whole exome sequencing of a trio and singleton
Other
2014-06-05
EGAS00001000853
Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
Other
2014-06-06
EGAS00001000854
Systems biology of Colorectal Cancer
Other
2014-06-10
EGAS00001000855
Genomic landscape of Ewing sarcoma (ICGC project)
Other
2014-06-10
EGAS00001000857
Deep_sequencing_of_melanoma_for_driver_mutations
Cancer Genomics
2014-06-12
EGAS00001000858
Integrative_genome_profiling_in_AML
Cancer Genomics
2014-06-12
EGAS00001000859
Anaplastic_Meningioma_WGS_X10
Cancer Genomics
2014-06-12
EGAS00001000860
Use_of_deep_sequencing_to_detect_clonal_mutations_in_sun_exposed_human_epidermis___whole_genome
Cancer Genomics
2014-06-12
EGAS00001000864
The_life_history_of_colorectal_cancer_metastases_study_WGS_X10
Cancer Genomics
2014-06-18
EGAS00001000865
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Other
2014-06-18
EGAS00001000866
HipSci HumanExome BeadChip analysis-Healthy volunteers
Other
2014-06-18
EGAS00001000867
HipSci HumanHT_12v4 Expression BeadChip analysis-Healthy volunteers
Other
2014-06-18
EGAS00001000869
Colorectal_organoids_and_tumoroids___pulldown
Cancer Genomics
2014-06-25
EGAS00001000870
BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils
Other
2014-06-25
EGAS00001000872
Chugai_colorectal_organoid_sequencing
Cancer Genomics
2014-06-26
EGAS00001000874
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Cancer Genomics
2014-07-01
EGAS00001000875
Loss of functional mutation in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan Anemia
Other
2014-07-02
EGAS00001000876
Characterization_of_iPSC_derived_macrophages___cardiovascular_pilot
Transcriptome Analysis
2014-07-02
EGAS00001000877
Whole genome DNA sequencing for two long-lived humans.
Other
2014-07-02
EGAS00001000878
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Other
2014-07-03
EGAS00001000879
Prognostic_factors_in_prostate_cancer__deep_sequencing_pilot_project_TAPG
Cancer Genomics
2014-07-03
EGAS00001000880
Myeloma_Targeted_Follow_up_Study
Cancer Genomics
2014-07-03
EGAS00001000881
Colorectal_organoids_and_tumour_tissue
Cancer Genomics
2014-07-03
EGAS00001000882
Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Other
2014-07-07
EGAS00001000883
Study on the proliferation history of colorectal adenomas
Other
2014-07-07
EGAS00001000884
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Other
2014-07-08
EGAS00001000885
Whole Genome Sequencing to track subclonal heterogeneity in 18 samples from 3 Chronic Lymphocytic Leukemia patients subjected to repeated cycles of therapy.
Other
2014-07-08
EGAS00001000886
WTCCC2 Reading and Mathematics (RM) samples
Other
2014-07-10
EGAS00001000888
65 prostate cancer cases WGS and transcriptome sequencing project
Other
2014-07-16
EGAS00001000889
TEST_STUDY for submitter testing
Other
2014-07-21
EGAS00001000890
Multisite_Breast_Cancer_Whole_Genome
Cancer Genomics
2014-07-21
EGAS00001000891
Multisite_Primary_Breast_Cancer
Cancer Genomics
2014-07-21
EGAS00001000892
Chordoma_Extension_Study
Cancer Genomics
2014-07-23
EGAS00001000895
Chordoma_Extension__known_cancer_genes_
Cancer Genomics
2014-07-23
EGAS00001000896
An isolated cohort of samples from the Greek island of Crete that have been genotyped on the Illumina CoreExome array.
Other
2014-07-23
EGAS00001000899
SeqControl: Process Control for DNA Sequencing
Other
2014-07-23
EGAS00001000900
Canadian Prostate Cancer Genome Network
Other
2014-07-23
EGAS00001000901
The Genomic Landscape of Childhood and Adolescent Melanoma
Other
2014-07-23
EGAS00001000902
Metastatic_Breast_Cancer_Whole_Genome
Cancer Genomics
2014-07-23
EGAS00001000904
Exome sequencing to identify predisposition to Wilms tumour
Other
2014-07-24
EGAS00001000906
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors
Other
2014-07-28
EGAS00001000907
Von Hippel-Lindau syndrome multi-region exome sequencing project from two patients undertaken at Cancer Research UK's London Research Institute
Other
2014-07-29
EGAS00001000908
Evolution of the African pygmy phenotype
Other
2014-07-29
EGAS00001000909
Normal brain controls for ICGC PedBrain DNA methylation sequencing
Other
2014-07-30
EGAS00001000910
DNA methylation repeatability in the Lothian Birth Cohorts of 1921 and 1936.
Other
2014-07-30
EGAS00001000913
WTCCC3_Anorexia_Nervosa
Population Genomics
2014-07-31
EGAS00001000916
Developmental_Dysplasia_of_the_Hip__DDH_
Population Genomics
2014-07-31
EGAS00001000917
ARGO_GWAS
Population Genomics
2014-07-31
EGAS00001000918
Genome_wide_association_study_of_vaccine_responses_in_infants_living_in_the_Developing_World__VaccGene___Phase_II_African_Cohorts
Population Genomics
2014-07-31
EGAS00001000924
Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014
Other
2014-07-31
EGAS00001000925
Comprehensive genomic profiles of small cell lung cancer
Other
2014-07-31
EGAS00001000926
Study of non-clear cell renal cell carcinoma
Other
2014-08-01
EGAS00001000927
A Comparative Analysis of Algorithms for Somatic SNV Detection in Cancer
Other
2014-08-04
EGAS00001000930
Intra-tumor heterogeneity of localized lung adenocarcinomas defined by multi-region sequencing
Other
2014-08-05
EGAS00001000932
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Other
2014-08-06
EGAS00001000933
Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas
Other
2014-08-07
EGAS00001000934
PREDICT___Whole_Genomes
Cancer Genomics
2014-08-07
EGAS00001000935
Single_Cell_Sequencing_of_Sperm__scSperm_
Population Genomics
2014-08-08
EGAS00001000936
Ischemic stroke in a Swedish case-control study.
Other
2014-08-10
EGAS00001000938
Whole Exome Sequencing of healthy Spanish individuals
Other
2014-08-11
EGAS00001000940
Whole genome study of Hurthle cell thyroid carcinoma
Other
2014-08-12
EGAS00001000941
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Other
2014-08-14
EGAS00001000942
Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer
Other
2014-08-15
EGAS00001000943
Genomic analysis of seminomas
Other
2014-08-18
EGAS00001000946
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Cancer Genomics
2014-08-22
EGAS00001000947
ATAC_SEQ_MAIN___PHASE_1
Transcriptome Analysis
2014-08-23
EGAS00001000948
DKFZ-HIPO Project H021/NCT MASTER
Other
2014-08-26
EGAS00001000949
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Other
2014-08-28
EGAS00001000950
Whole exome and transcriptome sequencing of biliary tract cancer
Other
2014-08-29
EGAS00001000951
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Other
2014-08-29
EGAS00001000952
Dynamics of genomic clones in breast cancer patient xenografts at single cell resolution
Other
2014-08-29
EGAS00001000953
BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Other
2014-09-01
EGAS00001000954
BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Other
2014-09-01
EGAS00001000955
EBV_AID_project
Cancer Genomics
2014-09-03
EGAS00001000957
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Other
2014-09-04
EGAS00001000958
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Cancer Genomics
2014-09-05
EGAS00001000959
APCDR AGV Project: The African Genome Variation Project(dense array genotyping data)
Other
2014-09-05
EGAS00001000960
APCDR AGV Project: Whole genome sequencing of 3 African populations (curated data)
Other
2014-09-05
EGAS00001000961
Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes
Other
2014-09-05
EGAS00001000962
Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing
Other
2014-09-06
EGAS00001000963
The Druze analysis group
Other
2014-09-08
EGAS00001000968
Origins and functional consequence of somatic mitochondrial DNA mutations
Other
2014-09-10
EGAS00001000969
HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Other
2014-09-10
EGAS00001000971
Exome sequencing of 1000 population control samples from the UK 1958 birth cohort
Other
2014-09-15
EGAS00001000973
High coverage target resequencing of coding and regulatory regions of 38 Parkinson disease genes associated either to the Mendelian or the sporadic forms of the disease
Other
2014-09-16
EGAS00001000974
Genetic landscape of malignant peripheral nerve sheath tumors
Other
2014-09-17
EGAS00001000975
Signatures of Aristolochic Acid Mutagenesis in Bladder Cancer
Other
2014-09-18
EGAS00001000978
Cancer_Cell_Line_Exome_Sequencing_
Cancer Genomics
2014-09-19
EGAS00001000979
Pulldown_DNA_methylation_study_v2
Cancer Genomics
2014-09-19
EGAS00001000980
Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))
Other
2014-09-22
EGAS00001000981
We evaluate the PGD/PGS including 129 couples with NGS test and 266 couples with SNP-array test for the detection of embryonic chromosomal abnormalities.
Other
2014-09-23
EGAS00001000982
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Other
2014-09-24
EGAS00001000983
SOFT_study___sequencing_premenopausal_breast_cancer
Cancer Genomics
2014-09-24
EGAS00001000985
_RNAseq___Colorectal_organoids_and_tumoroids
Cancer Genomics
2014-09-24
EGAS00001000988
30X_WGS_sequencing_of_100_individuals_from_the_general_Greek_population
Other
2014-09-26
EGAS00001000990
Fetal hemoglobin in sickle cell disease patients from Tanzania
Other
2014-09-26
EGAS00001000991
Therapeutic Resistance to PI3K-alpha Inhibitors
Other
2014-09-26
EGAS00001000992
Human melanoma samples with and without resistance to BRAF inhibitor therapy
Other
2014-09-26
EGAS00001000993
Identification of causal mutation in two patients with Sotos Syndrome Features
Other
2014-09-29
EGAS00001000995
McGill Epigenomics Mapping Centre
Other
2014-10-01
EGAS00001000996
Illumina HumanOmniExpress genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study.
Other
2014-10-03
EGAS00001001000
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Other
2014-10-08
EGAS00001001001
Illumina HumanCoreExome genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study.
Other
2014-10-09
EGAS00001001002
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets
Other
2014-10-09
EGAS00001001003
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Other
2014-10-09
EGAS00001001004
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Other
2014-10-10
EGAS00001001009
Biased allelic expression in human primary fibroblast single cells.
Other
2014-10-14
EGAS00001001011
MDS Sequencing Project_Cancer Cell
Other
2014-10-17
EGAS00001001012
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Other
2014-10-20
EGAS00001001013
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness
Other
2014-10-20
EGAS00001001014
Spatial heterogeneity in medulloblastoma
Other
2014-10-21
EGAS00001001015
Exomes of High-risk Prostate cancer
Other
2014-10-23
EGAS00001001016
A Cancer Cell-Line Titration Series for Evaluating Somatic Classification
Exome Sequencing
2014-10-23
EGAS00001001017
Genotype data of osteoarthritis cases from the UK collected by the arcOGEN Consortium (http://www.arcogen.org.uk/).
Other
2014-10-27
EGAS00001001018
Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer
Other
2014-10-29
EGAS00001001019
(h)MeDIP-Seq of high-risk prostate cancer
Other
2014-10-29
EGAS00001001020
Genome-wide prediction of human embryos
Other
2014-10-30
EGAS00001001021
Exome_sequencing_of_EBV_driven_lymphoma
Cancer Genomics
2014-10-30
EGAS00001001023
Whole genome sequencing of ASD quartet families
Other
2014-10-31
EGAS00001001024
Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients
Other
2014-10-31
EGAS00001001025
Comprehensive miRNA Sequence Analysis Reveals Survival Differences in Diffuse Large B-cell Lymphoma Patients
Other
2014-10-31
EGAS00001001026
Prediction and quantification of splice events from RNA-seq data
Other
2014-10-31
EGAS00001001028
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR02
Other
2014-11-03
EGAS00001001033
Spatial and temporal genomic evolution in glioblastoma
Other
2014-11-09
EGAS00001001035
Identification_of_drug_resistance_genes_in_cancer_cell_lines_by_insertional_mutagenesis
Cancer Genomics
2014-11-12
EGAS00001001036
English Longitudinal Study of Ageing Genome-wide genotyping using the Illumina HumanOmni2.5-8
Other
2014-11-13
EGAS00001001041
Spatio-temporal evolution of the primary glioblastoma genome
Other
2014-11-17
EGAS00001001044
To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 291 SNP-array were performed.
Other
2014-11-19
EGAS00001001045
To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 293 SNP-array were performed.
Other
2014-11-19
EGAS00001001047
Finnish_population_cohort_genotyping_B
Population Genomics
2014-11-19
EGAS00001001048
Preeclampsia InterPregGen Consortium: GWAS meta-analysis summary statistics for European fetal preeclampsia cases versus controls and GWAS genotype data for European fetal preeclampsia cases
Other
2014-11-19
EGAS00001001051
Methylation differences in trisomy 21 using monozygotic twins
Other
2014-11-26
EGAS00001001052
Skin Adenocarcinoma Genome Sequencing
Other
2014-12-01
EGAS00001001054
GIST_SSGXVIII_trial_targeted_gene_sequencing
Cancer Genomics
2014-12-02
EGAS00001001056
WGS and WES of 78 pairs Chinese gastric cancer
Other
2014-12-04
EGAS00001001059
Cell_lines_with_telomere_fusion_induced_rearrangements
Cancer Genomics
2014-12-04
EGAS00001001060
CRISPR_screen_M14__NCI_H3122
Cancer Genomics
2014-12-04
EGAS00001001066
Genome-wide SNP genotyping and DNA methylation epigenotyping of African rainforest hunter-gatherers and neighbouring agriculturalists
Other
2014-12-05
EGAS00001001067
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Other
2014-12-08
EGAS00001001077
The mission of the BIOS Consortium is to create a large-scale data infrastructure and to bring together BBMRI researchers focusing on integrative omics studies in Dutch Biobanks.
Other
2014-12-09
EGAS00001001082
2014 chunnam AML analysis
Other
2014-12-10
EGAS00001001084
Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Other
2014-12-10
EGAS00001001085
Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci
Other
2014-12-10
EGAS00001001086
Exome_sequencing_of_short_SGA_children_with_IGF_I_and_insulin_resistance
Other
2014-12-10
EGAS00001001090
GWAS of tuberculosis in Russia
Other
2014-12-15
EGAS00001001093
Exome Sequencing Of 75 Individuals From Multiply Affected Coeliac Families
Other
2014-12-16
EGAS00001001095
NGS_based_viability_screening_using_haploid_cell_line
Cancer Genomics
2014-12-16
EGAS00001001099
ABIS_1_MeDIP-seq
Other
2014-12-17
EGAS00001001102
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Other
2014-12-19
EGAS00001001103
Whole-exome sequencing of Fanconi anemia
Other
2014-12-28
EGAS00001001108
Exome Sequencing Reveals Frequent Inactivating Mutations in BAP1, ARID1A, and PBRM1 in Intrahepatic Cholangiocarcinomas
Other
2015-01-08
EGAS00001001110
Blueprint RNAseq profile of purified plasma cells from multiple myeloma patients and tonsils of healthy donors
Other
2015-01-09
EGAS00001001112
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Other
2015-01-12
EGAS00001001113
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Other
2015-01-13
EGAS00001001114
Whole_exome_sequencing_of_additional_thyroid_disease_cases
Other
2015-01-13
EGAS00001001115
Genetic_profiling_of_mucosal_melanoma
Other
2015-01-14
EGAS00001001116
ESGI___Whole_Genome_Sequencing_of_samples_from_the_Cilentogen_isolates
Population Genomics
2015-01-14
EGAS00001001117
ESGI___Whole_Genome_Sequencing_of_NSPHS_samples
Population Genomics
2015-01-14
EGAS00001001119
ESGI___Whole_Genome_Sequencing_of_samples_from_the_Croatian_isolated_populations_
Population Genomics
2015-01-14
EGAS00001001123
ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_
Population Genomics
2015-01-14
EGAS00001001124
Congenital_anosmia_1
Other
2015-01-14
EGAS00001001125
ESGI___Whole_Genome_Sequencing_of_samples_from_the_ORCADES_cohort__X10__
Cancer Genomics
2015-01-14
EGAS00001001127
MiR expression profiles of paired primary colorectal cancerand metastases by next-generation sequencing
Other
2015-01-19
EGAS00001001129
IBDCA_Edinburgh
Other
2015-01-20
EGAS00001001130
Genome-wide association study of response to warfarin in a UK prospective cohort
Other
2015-01-21
EGAS00001001132
DPY30_ChIP_seq
Epigenetics
2015-01-22
EGAS00001001133
mFAST-SeqS
Other
2015-01-22
EGAS00001001134
Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Other
2015-01-22
EGAS00001001135
Intratumor heterogeneity evaluation in primary HCC cells
Other
2015-01-23
EGAS00001001137
HipSci___RNAseq___Rare_Monogenic Diabetese
Other
2015-01-26
EGAS00001001139
Whole genome and RNA sequencing of paediatric glioblastoma in the ICGC PedBrain project
Other
2015-01-26
EGAS00001001140
HipSci___Whole_Exome_sequencing___Monogenic_Diabetes
Other
2015-01-26
EGAS00001001145
FWO_project_G_0687_12_X10_WGS
Cancer Genomics
2015-01-29
EGAS00001001146
Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia
Other
2015-01-30
EGAS00001001147
463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Other
2015-02-02
EGAS00001001149
Mapping_regulatory_variation_in_sensory_neurons_using_IPS_lines_from_the_HIPSCI_project
Gene Regulation Study
2015-02-05
EGAS00001001150
A personalised medicine approach for ponatinib-resistant chronic myeloid leukaemia
Other
2015-02-05
EGAS00001001153
Aplastic anemia
Other
2015-02-10
EGAS00001001155
Anaplastic_Meningioma_V3__cancer_gene_panel
Cancer Genomics
2015-02-11
EGAS00001001158
Leeds_Melanoma_Cohort
Cancer Genomics
2015-02-12
EGAS00001001159
The BC Cancer Agency's Personalized Onco-Genomics Project
Cancer Genomics
2015-02-19
EGAS00001001165
Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations
Other
2015-02-19
EGAS00001001167
The Berlin (BLN) panel of glioblastoma cell lines: RNAseq of human gliomasphere cell lines and matched parental tumors
Other
2015-02-19
EGAS00001001168
GWAS study on arsenic-exposed population
Other
2015-02-20
EGAS00001001170
Recursive splicing in long vertebrate genes
Other
2015-02-23
EGAS00001001171
Mutational_Analysis_of_Colorectal_PDX_models
Cancer Genomics
2015-02-24
EGAS00001001172
Sequencing of heritable Bleeding and Platelet Disorders
Other
2015-02-24
EGAS00001001173
Reference_DNA_standards_for_GCLP_pipeline
Cancer Genomics
2015-02-26
EGAS00001001174
Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Other
2015-02-26
EGAS00001001176
Study of renal cancers and renal cancer metastases
Other
2015-02-27
EGAS00001001178
560 whole-genome sequenced breast cancers
Other
2015-03-02
EGAS00001001179
Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Other
2015-03-03
EGAS00001001180
Methylation_changes_in_OA_patients_with_chronic_exposure_to_cobalt_and_chromium
Population Genomics
2015-03-05
EGAS00001001182
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Population Genomics
2015-03-08
EGAS00001001183
Neuroblastoma relapse trio series from the AMC
Other
2015-03-08
EGAS00001001184
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Other
2015-03-09
EGAS00001001190
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
Other
2015-03-10
EGAS00001001191
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Other
2015-03-10
EGAS00001001194
Exome sequencing
Other
2015-03-12
EGAS00001001195
ICGC Breast Cancer Project
Other
2015-03-12
EGAS00001001196
BLUEPRINT DNA methylation profiling of B-cell differentiation using Illumina HumanMethylation 450K BeadArray
Other
2015-03-13
EGAS00001001197
BLUEPRINT Gene expression analysis during human B-cell differentiation using the Affymetrix Human Genome U219 Array
Other
2015-03-13
EGAS00001001199
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Other
2015-03-20
EGAS00001001202
CONSERTING: integrating copy number analysis with structural variation detection
Other
2015-03-24
EGAS00001001203
Pilot_experiment_on_functional_genomics_in_osteoarthritis_RNA
Transcriptome Analysis
2015-03-25
EGAS00001001204
G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Whole Genome Sequencing
2015-03-26
EGAS00001001205
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Other
2015-03-26
EGAS00001001206
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Other
2015-03-27
EGAS00001001207
15x_WGS_HELIC_MANOLIS_
Whole Genome Sequencing
2015-03-27
EGAS00001001209
Anaplastic oligodendroglioma exome and RNA sequencing data
Metagenomics
2015-03-27
EGAS00001001210
Whole Genome sequencing of adult T-cell leukemia/lymphoma
Other
2015-03-30
EGAS00001001212
Pilot_experiment_on_functional_genomics_in_osteoarthritis
Population Genomics
2015-03-30
EGAS00001001213
Pilot_experiment_on_functional_genomics_in_osteoarthritis
Population Genomics
2015-03-30
EGAS00001001214
Whole genome and transcriptome analysis of anaplastic thyroid carcinoma
Other
2015-04-03
EGAS00001001218
Validation_for_human_early_embryonic_substitutions_
Cancer Genomics
2015-04-10
EGAS00001001219
Deconvolution
Other
2015-04-14
EGAS00001001223
LINE_luminal_breast_cancer_Neoadjuvant_Chemotherapy_Study
Cancer Genomics
2015-04-15
EGAS00001001231
Yemen_and_Chad_Genotyping
Cancer Genomics
2015-04-15
EGAS00001001232
Understanding_Society_GWAS
Other
2015-04-16
EGAS00001001234
Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Other
2015-04-20
EGAS00001001235
Associations between APOE status and cognitive ability across the lifecourse
Other
2015-04-21
EGAS00001001236
Comprehensive Transcriptional Analysis of Early Stage Urothelial Carcinoma using whole transcriptome sequencing
Other
2015-04-21
EGAS00001001237
SNP genotyping of multiplex autoimmune Addison's families from the UK and Norway
Other
2015-04-23
EGAS00001001238
Targeted_replication_of_LVOTO_genes
Other
2015-04-23
EGAS00001001240
Exploring the role of mtDNA variation in Multiple Sclerosis in a large cohort of discordant monozygotic twins
Metagenomics
2015-04-26
EGAS00001001242
The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer
Other
2015-04-30
EGAS00001001244
Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Other
2015-05-04
EGAS00001001245
Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts
Other
2015-05-04
EGAS00001001247
Papuan Genomes: whole genome sequencing
Other
2015-05-07
EGAS00001001250
Exome Sequencing in Moebius Syndrome
Other
2015-05-08
EGAS00001001251
Leucocyte eQTLs in autoimmune disease and health
Other
2015-05-09
EGAS00001001252
Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Other
2015-05-11
EGAS00001001253
Microinjection_of_hIPSC_derived_intestinal_organoids_with_Salmonella_Typhimurium
Transcriptome Analysis
2015-05-13
EGAS00001001254
Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy
Other
2015-05-13
EGAS00001001255
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Other
2015-05-13
EGAS00001001256
Genetic_screening__of_GPI_anchor_protein_synthesis__
Other
2015-05-14
EGAS00001001257
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Other
2015-05-15
EGAS00001001258
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Other
2015-05-18
EGAS00001001260
Understand_Paratyphoid_Disease___host_responses_to_human_challenge_with_S__Paratyphi_A
Transcriptome Analysis
2015-05-19
EGAS00001001261
Colorectal_Adenoma_Gene_Screen
Cancer Genomics
2015-05-19
EGAS00001001262
Deciphering the mutational landscape and the genome organization of LMS
Other
2015-05-20
EGAS00001001263
Exome_Sequencing_of_Human_myeloid_malignancies
Cancer Genomics
2015-05-20
EGAS00001001264
CMML Collection of WES, WGS, RNA-Seq and ERRBS data
Other
2015-05-20
EGAS00001001265
cis-eQTL mapping of human pancreatic islets
Metagenomics
2015-05-21
EGAS00001001266
Preeclampsia InterPregGen Consortium: Large-scale GWAS meta-analysis of maternal preclampsia cases and controls from Europe and Central Asia. Plus extension of earlier European fetal preeclampsia GWAS meta-analysis (see EGAS00001001048) by adding Central Asian fetal preeclampsia cases and controls. Datasets provided under this study are GWAS meta-analysis summary statistics and individual level GWAS genotype data. Related InterPregGen Consortium data are also provided under studies EGAS00001000416 and EGAS00001000417 (whole genome sequence data for 100 unrelated Uzbeks and 100 unrelated Kazakhs) and EGAS00001001048 (European fetal preeclampsia GWAS summary statistics and genotype data
Other
2015-05-22
EGAS00001001268
Whole exome sequencing of papillary thyroid carcinoma in the Chinese population
Other
2015-05-25
EGAS00001001272
HipSci HumanExome BeadChip analysis-Rare_BBS
Other
2015-06-04
EGAS00001001273
HipSci HumanExome BeadChip analysis - monogenic diabetes
Other
2015-06-04
EGAS00001001274
HipSci Illumina 450K Methylation analysis-Rare_BBS
Other
2015-06-04
EGAS00001001275
HipSci Illumina 450K Methylation analysis - monogenic diabetes
Other
2015-06-04
EGAS00001001276
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Other
2015-06-04
EGAS00001001277
HipSci HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes
Other
2015-06-04
EGAS00001001279
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Other
2015-06-06
EGAS00001001281
PLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma
Other
2015-06-08
EGAS00001001283
IL_10_signalling_and_macrophage_gene_expression
Transcriptome Analysis
2015-06-09
EGAS00001001284
Recurrent adeno-associated virus 2-related insertional mutagenesis in human hepatocellular carcinomas
Other
2015-06-09
EGAS00001001285
Ribosome_Profiling_of_Macrophages_during_Salmonella_Infection
Whole Genome Sequencing
2015-06-10
EGAS00001001287
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Other
2015-06-12
EGAS00001001288
Induced Pluripotent Cells Derived from Differentiated Rod Photoreceptors Undergo Efficient Retinogenesis in Three-Dimensional Cultures
Other
2015-06-12
EGAS00001001289
Targeted_Sequencing_of_Human_Myeloid_Malignancies
Cancer Genomics
2015-06-17
EGAS00001001292
SNP genotyping data in genes related to trace element homeostasis
Other
2015-06-19
EGAS00001001293
Growth Hormone (GH) -secreting Pituitary Adenoma
Other
2015-06-22
EGAS00001001294
Transcriptome_human_nasal_epithelium
Transcriptome Analysis
2015-06-22
EGAS00001001296
Integrated molecular analysis of adult T-cell leukemia/lymphoma
Other
2015-06-22
EGAS00001001297
Comprehensive analysis of the (epi)genome of pediatric atypical teratoid/rhabdoid tumours (AT/RTs)
Other
2015-06-23
EGAS00001001299
Multiple_Myeloma_Diagnosis_to_Relapse_study_samples
Cancer Genomics
2015-06-25
EGAS00001001301
PRDM9_loss_of_function_follow_up_from_Born_in_Bradford_Autozygosity_sequencing
Whole Genome Sequencing
2015-06-25
EGAS00001001302
Identification of four new susceptibility loci for testicular germ cell tumour, including variants near GAB2, GSPT1 and ZFPM1
Other
2015-06-30
EGAS00001001303
Accurate sample assignment in a multiplexed, ultra-sensitive, high-throughput sequencing assay for minimal residual disease
Other
2015-06-30
EGAS00001001304
Resistance_to_MAPK_inhibitor_induces_internal_duplication_in_BRAF
Other
2015-07-01
EGAS00001001305
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Other
2015-07-01
EGAS00001001306
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Other
2015-07-02
EGAS00001001308
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Other
2015-07-06
EGAS00001001310
Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells
Other
2015-07-09
EGAS00001001311
Genome-wide study of resistance to severe malaria in eleven worldwide populations
Other
2015-07-13
EGAS00001001314
Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Other
2015-07-20
EGAS00001001315
Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Other
2015-07-20
EGAS00001001316
Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia
Other
2015-07-20
EGAS00001001317
Genomic landscape of childhood acute lymphoblastic leukemia
Other
2015-07-21
EGAS00001001318
HipSci___RNAseq___Rare_BBS
Transcriptome Analysis
2015-07-22
EGAS00001001323
Whole_Genome_Sequencing_of_JK_Family
Whole Genome Sequencing
2015-07-23
EGAS00001001324
JMML targeted sequencing (2013)
Other
2015-07-23
EGAS00001001329
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Other
2015-07-27
EGAS00001001332
A collection of 142 samples used to evaluate the sensitivity and specificity of small-scale variation detection in exome-capture data with a particular focus on indel detection.
Other
2015-07-27
EGAS00001001340
Genomic analysis of HPV positive versus HPV negative esophageal adenocarcinoma
Other
2015-07-29
EGAS00001001343
Somatic_Genetics_of_lesions_from_a_POT1_patient
Cancer Genomics
2015-07-30
EGAS00001001348
Melanoma_multi_site_metastases
Cancer Genomics
2015-07-31
EGAS00001001353
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Other
2015-08-03
EGAS00001001354
Genome-wide association data on male-pattern baldness
Other
2015-08-03
EGAS00001001355
Whole_Genome_Sequencing_of_INTERVAL
Whole Genome Sequencing
2015-08-03
EGAS00001001382
OCCAMS_Oesophageal_Cancer_Organoids_1
Cancer Genomics
2015-08-06
EGAS00001001385
A somatic reference standard for cancer genome sequencing with COLO829
Other
2015-08-06
EGAS00001001386
Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis
Other
2015-08-06
EGAS00001001387
Genomes of Relapsing Neuroblastoma
Other
2015-08-10
EGAS00001001394
Genome-wide identification of distinct miRNA-mRNA target regulation pairs in Non-Hodgkin lymphomas: a report from the ICGC MMML-Seq consortium
Other
2015-08-13
EGAS00001001418
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Other
2015-08-19
EGAS00001001422
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Cancer Genomics
2015-08-20
EGAS00001001427
Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Other
2015-08-25
EGAS00001001429
Congenital_anosmia_2
Other
2015-08-26
EGAS00001001431
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Other
2015-08-28
EGAS00001001433
Fixative optimisation study for BRITROC project
Other
2015-08-28
EGAS00001001436
Multiregion Whole Exome sequencing of paediatric High Grade Gliomas and DIPG
Other
2015-09-01
EGAS00001001437
Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A
Other
2015-09-01
EGAS00001001456
BLUEPRINT EpiVar 450K DNA methylation profiles of naive CD4+ T-cells, monocytes & neutrophils
Other
2015-09-04
EGAS00001001457
Genetic and epigenetic characterization of adenoid cystic carcinoma
Other
2015-09-04
EGAS00001001458
GENETIC HISTORY OF ITALY
Other
2015-09-08
EGAS00001001459
GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Other
2015-09-08
EGAS00001001460
T2D-GENES: Exome sequencing
Other
2015-09-08
EGAS00001001461
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Other
2015-09-09
EGAS00001001462
Targeting PTPRK-RSPO3 colon tumours promotesdifferentiation and loss of stem-cell function
Other
2015-09-09
EGAS00001001463
Exome-sequencing of human B cell lymphoma cell lines
Other
2015-09-10
EGAS00001001465
HipSci - Human Induced Pluripotent Stem Cells Initiative
Other
2015-09-11
EGAS00001001466
Sequencing of serial plasma and multiregional tumor samples in a patient with metastatic breast cancer
Other
2015-09-12
EGAS00001001472
Analysis of the lung gene expression profile in COPD
Other
2015-09-18
EGAS00001001473
Whole genome and transcriptome analysis of medullary thyroid cancer
Other
2015-09-18
EGAS00001001474
WGS-Lung Cancer sample 30 pair
Other
2015-09-20
EGAS00001001475
71 Whole-exome sequencing of Esophageal Squamous Cell Carcinoma on Chinese Patients
Other
2015-09-20
EGAS00001001476
TraIT Cell Line use case
Other
2015-09-21
EGAS00001001479
TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors
Other
2015-09-28
EGAS00001001486
Transcriptomics_of_human_olfactory_mucosa
Transcriptome Analysis
2015-09-29
EGAS00001001487
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Other
1980-01-01
EGAS00001001501
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Other
1980-01-01
EGAS00001001515
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Other
2015-09-30
EGAS00001001516
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Other
2015-09-30
EGAS00001001519
Glioblastoma_CRISPR_Screen
Cancer Genomics
1980-01-01
EGAS00001001520
BAP1_sequence_of_uveal_melanoma_cell_lines
Cancer Genomics
1980-01-01
EGAS00001001521
S_CORT_Stratification_in_COloRecTal_cancer_
Cancer Genomics
2015-10-01
EGAS00001001537
RNA_expression_profiling_of_melanoma_patient_derived_xenograft
Transcriptome Analysis
1980-01-01
EGAS00001001539
A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Other
1980-01-01
EGAS00001001540
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Other
1980-01-01
EGAS00001001542
Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified
Other
2015-10-07
EGAS00001001552
Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Other
2015-10-09
EGAS00001001553
Genetic landscape of relapsed DLBCL
Other
2015-10-10
EGAS00001001558
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Other
2015-10-12
EGAS00001001559
AML_WES
Other
2015-10-14
EGAS00001001561
PSCP_mutation_analysis_in_hESCs
Whole Genome Sequencing
2015-10-16
EGAS00001001563
Genomic characterization of Malignant Pleural Mesothelioma.
Other
1980-01-01
EGAS00001001565
The_British_Autozygosity_Populations_BioResource
Other
2015-10-19
EGAS00001001568
reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4+ memory T-Cells
Other
1980-01-01
EGAS00001001569
Population whole-genome bisulfite sequencing across two tissues highlights environment as principal source of human methylome variation
Other
1980-01-01
EGAS00001001570
Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Other
2015-10-24
EGAS00001001572
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Other
2015-10-28
EGAS00001001573
The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Cancer Genomics
1980-01-01
EGAS00001001575
Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Other
2015-10-30
EGAS00001001585
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Other
1980-01-01
EGAS00001001587
Papuan_Genotyping
Population Genomics
2015-11-03
EGAS00001001588
Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Other
1980-01-01
EGAS00001001590
TTV018_RORC_IBD_associated_genotype_effects_on_RORgT_expression_and_function_in_ex_vivo_T_cells
Transcriptome Analysis
1980-01-01
EGAS00001001591
RNAseq_of_ribosomal_footprints
Cancer Genomics
1980-01-01
EGAS00001001595
Epigenetic dynamics of monocyte to macrophage differentiation
Other
1980-01-01
EGAS00001001596
BLUEPRINT ATAC-seq data for cells in the haematopoietic lineages, from adult and cord blood samples
Other
1980-01-01
EGAS00001001597
Low_depth_whole_genome_sequencing_across_multiple_isolated_populations
Whole Genome Sequencing
1980-01-01
EGAS00001001598
BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins
Other
2015-11-10
EGAS00001001599
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Other
2015-11-11
EGAS00001001600
Container Study for ICGC Malignant Lymphoma Master Study (MMML)
Other
2015-11-12
EGAS00001001601
Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Other
1980-01-01
EGAS00001001603
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Other
2015-11-19
EGAS00001001604
Identifying_new_diagnostic_and_treatment_pathways_for_patients_with_unclassifiable_sarcomas
Cancer Genomics
2015-11-19
EGAS00001001605
Targeted sequencing of 12 genes in patients with HLH
Other
1980-01-01
EGAS00001001606
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Other
1980-01-01
EGAS00001001607
Targeted sequencing of brain expressed miRNA genes
Other
1980-01-01
EGAS00001001608
All available datasets of DEEP
Other
1980-01-01
EGAS00001001610
We screened 2.5 million SNPs in 161 individuals from 13 Sahelian populations from Western, Central and Eastern parts of the belt, and including both nomadic and sedentary groups
Other
2015-11-24
EGAS00001001611
FetalQuant-SD: Accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA
Other
2015-11-26
EGAS00001001612
Exome sequencing of uterine leiomyosarcomas
Other
2015-11-26
EGAS00001001613
GILD_ExomeSeq_PTNHL
Cancer Genomics
2015-11-26
EGAS00001001614
Melanoma_C32_ENU_resistance_to_Combination_Therapy
Cancer Genomics
2015-11-26
EGAS00001001615
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Other
2015-11-27
EGAS00001001623
Pediatric Whole Genome Sequencing Diagnostic Utility
Other
2015-12-01
EGAS00001001624
Epigenetic profiling of human CD4+ memory T cells reveals their proliferative history and argues in favor of a progressive differentiation model driven by epigenetically controlled master regulators.
Other
2015-12-02
EGAS00001001625
PSCP_bisulphite_analysis_in_hESCs
Epigenetics
2015-12-03
EGAS00001001632
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Other
2015-12-08
EGAS00001001637
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Other
2015-12-16
EGAS00001001638
BLUEPRINT Bisulfite-seq and Whole Genome Sequencing of mantle cell lymphoma
Other
2015-12-16
EGAS00001001639
Amplicon_based_sequencing_of_drug_resistant_organoids
Cancer Genomics
2015-12-16
EGAS00001001641
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Other
2015-12-17
EGAS00001001645
EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION
Other
2015-12-18
EGAS00001001653
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Other
2015-12-21
EGAS00001001654
Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pointine Glioma
Other
2015-12-21
EGAS00001001655
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Transcriptome Analysis
2015-12-22
EGAS00001001656
A unidirectional histone code in bidirectional promoters across cell types
Other
2015-12-22
EGAS00001001658
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Other
2015-12-28
EGAS00001001659
Integrated clinical, whole genome, and transcriptome analysis of multisampled lethal metastatic prostate cancer
Other
2016-01-01
EGAS00001001663
Population Structure and Genetic Diversity in Argentinean populations
Other
2016-01-07
EGAS00001001664
Investigating_the_genetics_of_immunity_against_Salmonella_in_humans
Whole Genome Sequencing
2016-01-07
EGAS00001001665
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Other
2016-01-07
EGAS00001001666
Large scale familial CRC exome sequencing study
Other
2016-01-08
EGAS00001001667
ICR MOPOPGEN UK exome control series
Other
2016-01-08
EGAS00001001675
Amplicon_based_sequencing_of_drug_resistant_lung_cancer_cell_lines
Cancer Genomics
2016-01-13
EGAS00001001676
Clonal_architecture_of_pre_malignant_and_malignant_tumours
Cancer Genomics
2016-01-15
EGAS00001001678
Comparison of HCC cell lines and primary HCCs
Other
2016-01-19
EGAS00001001682
Tissue-specific mutation accumulation in human adult stem cells during life
Other
2016-01-20
EGAS00001001686
Paired exome analysis in urothelial carcinoma
Other
2016-01-21
EGAS00001001687
Clonal_expansion_of_mutated_cell_population_in_bladder_urothelium_
Cancer Genomics
2016-01-22
EGAS00001001688
Genome_Diversity_in_Africa_Project__Benin
Whole Genome Sequencing
2016-01-25
EGAS00001001689
Flemish_Gut_Flora_Project
Other
2016-01-25
EGAS00001001690
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Other
2016-01-26
EGAS00001001692
ICGC PanCancer Analysis of Whole Genomes
Cancer Genomics
2016-01-29
EGAS00001001694
Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival.
Other
2016-02-01
EGAS00001001695
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Other
2016-02-02
EGAS00001001697
Melanoma_C32_ENU_Resistance_to_Single_Agent_Therapy
Cancer Genomics
2016-02-03
EGAS00001001698
Warm_Autopsy_Single_Cell_X10
Cancer Genomics
2016-02-03
EGAS00001001699
Genetic sequencing of MODY patients.
Other
2016-02-03
EGAS00001001700
Post-zygotic germline mutations in sperm
Other
2016-02-04
EGAS00001001701
Very short reads file for testing purposes
Other
2016-02-05
EGAS00001001702
Patient-derived conditionally reprogrammed cells (CRCs) were established and characterized to assess their biological properties and to apply these to test the efficacies of drugs.
Other
2016-02-06
EGAS00001001704
LifeLines-DEEP population multi-omix cohort from the noth of the Netherlands.
Other
2016-02-08
EGAS00001001706
Identification of gene mutations and fusion genes in patients with Sézary Syndrome
Other
2016-02-08
EGAS00001001708
RNA_seq_of_Toxoplasma_gondii_response_in_human_macrophages
Transcriptome Analysis
2016-02-10
EGAS00001001709
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Other
2016-02-10
EGAS00001001710
The Haplotype Reference Consortium
Other
2016-02-10
EGAS00001001711
Korean Young Age Diffuse Gastric Cancers
Other
2016-02-11
EGAS00001001713
PAGE: Prenatal Assessment of Genomes and Exomes
Other
2016-02-11
EGAS00001001714
WES analysis of a mixed cohort of pituitary tumors
Other
2016-02-12
EGAS00001001715
Copy number profiling of primary samples and cell lines of retinoblastoma
Other
2016-02-12
EGAS00001001723
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Other
2016-02-16
EGAS00001001726
HipSci whole exome sequencing for embryonic stem cell control lines
Other
2016-02-19
EGAS00001001727
HipSci RNA sequencing for embryonic stem cell control lines
Other
2016-02-19
EGAS00001001728
HipSci Methylation analysis for embryonic stem cell control lines
Other
2016-02-19
EGAS00001001729
HipSci expression microarray for embryonic stem cell control lines
Other
2016-02-19
EGAS00001001730
HipSci genotyping microarray for embryonic stem cell control lines
Other
2016-02-19
EGAS00001001732
Novel mutational mechanisms and drivers in Pancreatic Neuroendocrine Tumours
Other
2016-02-22
EGAS00001001733
120 individuals from the TEENAGE study (Ntalla et al., 2013) have been genotyped on the Illumina HumanCoreExome-12v1-1_A array. This is a population-based study of adolescents from the Attica region in Greece
Other
2016-02-22
EGAS00001001735
IBD_Whole_Genome_Sequencing_Phase_1
Other
2016-02-22
EGAS00001001736
Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing
Other
2016-02-24
EGAS00001001737
Exome-sequencing of two UFM individuals and their Fragile X family members.
Other
2016-02-25
EGAS00001001738
Multi-layered population structure in Island Southeast Asians
Other
2016-02-27
EGAS00001001740
Nrf2 transcript alterations
Other
2016-02-27
EGAS00001001741
Searching for variants associated with endometriosis
Other
2016-03-02
EGAS00001001742
We performed whole exome sequencing (WES) using Hiseq on 22 paired CMLs. We also performed whole exome sequencing (WES) using CG on 88 paired CMLs. All the data belongs to CML in China - ICGC project.
Other
2016-03-02
EGAS00001001743
ENU_CCK_81_cetuximab_pilot_project
Cancer Genomics
2016-03-02
EGAS00001001744
ENU_NCI_H508_cetuximab_fixed_concentration_project
Cancer Genomics
2016-03-02
EGAS00001001745
ENU_NCI_H508_Cetuximab_SecondRound
Cancer Genomics
2016-03-02
EGAS00001001746
Drug-perturbation-based stratification of blood cancer
Other
2016-03-03
EGAS00001001751
An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Other
2016-03-10
EGAS00001001752
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Other
2016-03-11
EGAS00001001753
METABRIC: Data from Pereira et al (2016), The somatic mutation profiles of 2433 breast cancers refine their genomic and transcriptomic landscapes. Nat Comms 7.
Other
2016-03-13
EGAS00001001754
Inferring expressed genes by whole-genome sequencing of plasma DNA
Other
2016-03-14
EGAS00001001755
Transcriptomes_of_human_lymphocytes
Transcriptome Analysis
2016-03-15
EGAS00001001756
WTCCC2 Bacteraemia Susceptibility (BS) samples
Other
2016-03-22
EGAS00001001757
Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas
Other
2016-03-22
EGAS00001001763
Longitudinal RNA-seq (whole blood) in a twin cohort
Other
2016-03-30
EGAS00001001764
The_mutational_landscape_of_recurrent_Glioblastome_multiforme
Cancer Genomics
2016-03-30
EGAS00001001765
Targeted_analysis_of_chondrosarcoma_cancer_genes
Cancer Genomics
2016-03-30
EGAS00001001766
A Genomic History of Aboriginal Australia
Other
2016-03-30
EGAS00001001767
Ashkenazi Jewish Leukoencephalopathy
Exome Sequencing
2016-03-30
EGAS00001001774
Korea Epigenome Project(KEP), Korea National Research Institute of Health(KNIH)
Other
2016-04-04
EGAS00001001777
ENU_LS_411N_TripleTherapy
Cancer Genomics
2016-04-12
EGAS00001001778
ENU_HT_29_BRAF_Triple_Therapy_Clones
Cancer Genomics
2016-04-12
EGAS00001001779
AML clonal phylogeny
Other
2016-04-13
EGAS00001001780
V2_panel_bait_design_test
Cancer Genomics
2016-04-14
EGAS00001001782
Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Other
2016-04-14
EGAS00001001783
Genome sequencing of HCC from a Chinese cohort
Other
2016-04-15
EGAS00001001784
Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Other
2016-04-19
EGAS00001001788
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Other
2016-04-24
EGAS00001001789
Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility
Other
2016-04-25
EGAS00001001791
ZhongShan Hospital liver tumor single cell sequencing.
Other
2016-04-27
EGAS00001001795
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Other
2016-04-27
EGAS00001001797
Targeted_gene_screen_of_drug_resistant_organoids
Cancer Genomics
2016-04-29
EGAS00001001799
Spiradenocarcinoma
Cancer Genomics
2016-04-29
EGAS00001001800
Spatio-temporal evolution of the primary glioblastoma genome (newly added after 2015)
Other
2016-05-01
EGAS00001001801
Comparing nodal versus bony metastatic spread using tumour phylogenies
Other
2016-05-04
EGAS00001001802
Native_American_Ancient_DNA_sequencing
Whole Genome Sequencing
2016-05-05
EGAS00001001803
Characterization of a human iPSC-derived endocrine pancreas model
Other
2016-05-05
EGAS00001001804
Interactions between the tumor and the systemic response of breast cancer patients
Other
2016-05-06
EGAS00001001805
A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma
Other
2016-05-09
EGAS00001001806
V2_Colorectal_panel_test
Cancer Genomics
2016-05-10
EGAS00001001807
V4_Colorectal_panel_test
Cancer Genomics
2016-05-10
EGAS00001001808
V4_panel_bait_design_test
Cancer Genomics
2016-05-10
EGAS00001001810
Clonal selection and double hit events involving tumor suppressor genes underlie relapse from total therapy
Other
2016-05-10
EGAS00001001821
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Other
2016-05-11
EGAS00001001822
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments
Other
2016-05-12
EGAS00001001828
Genome_Diversity_in_Africa_Project___GemCode_libraries_
Population Genomics
2016-05-13
EGAS00001001835
Whole exome sequencing of Finnish hereditary breast cancer families
Other
2016-05-17
EGAS00001001836
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Other
2016-05-17
EGAS00001001837
Dense_fine_mapping_study_identifies_new_susceptibility_loci_for_primary_biliary_cirrhosis
Population Genomics
2016-05-18
EGAS00001001838
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Other
2016-05-18
EGAS00001001839
Circulating Tumor DNA Analysis Detects Minimal Residual Disease and Predicts Recurrence in Patients with Stage II Colon Cancer
Other
2016-05-18
EGAS00001001840
RNA-seq analysis of megakaryocytes and granulocytes in Quebec platelet disorder
Other
2016-05-18
EGAS00001001841
The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Other
2016-05-19
EGAS00001001844
Targeting FGFR1 for treatment of soft-tissue sarcoma (H021)
Other
2016-05-23
EGAS00001001845
Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma (H021)
Other
2016-05-23
EGAS00001001846
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Other
2016-05-23
EGAS00001001847
Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia
Other
2016-05-23
EGAS00001001848
Evolution of a FLT3-TKD mutated subclone at meningeal relapse in acute promyelocytic leukemia (H021)
Other
2016-05-23
EGAS00001001849
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Other
2016-05-25
EGAS00001001852
Population_sequencing_phasing
Population Genomics
2016-05-26
EGAS00001001853
Australia_and_New_Guinea_haplotype_phasing_
Population Genomics
2016-05-26
EGAS00001001854
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Other
2016-05-26
EGAS00001001855
Low_input_LC__WGS_
Other
2016-05-27
EGAS00001001856
Low_input_LC__ISC_
Cancer Genomics
2016-05-27
EGAS00001001857
Genetic subclone heterogeneity of tumor-initiating cells in human colorectal cancer
Other
2016-05-29
EGAS00001001858
Whole transcriptome and exome sequencing of childhood ALL
Other
2016-05-31
EGAS00001001859
Transcriptome profiling for Korean Diffuse Gastric cancers
Other
2016-06-01
EGAS00001001861
Molecular evolution of metastatic clear cell renal cell carcinoma progressing under tyrosine kinase inhibitor therapy (HIPO-045)
Other
2016-06-01
EGAS00001001862
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Other
2016-06-01
EGAS00001001866
Subtype specific progression from DCIS to invasive breast cancer
Other
2016-06-07
EGAS00001001868
Recent genetic history of Denmark
Other
2016-06-08
EGAS00001001870
CD4+ T cell subsets stratified by complement receptor type 2 (CR2) expression
Other
2016-06-10
EGAS00001001871
Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Other
2016-06-21
EGAS00001001872
RNA sequencing data from visceral and abdominal subcutaneous adipose tissue from morbidly obese women with normal glucose tolerance or type 2 diabetes
Other
2016-06-21
EGAS00001001873
Transcriptome_analysis_of_anaplastic_meningiomas
Transcriptome Analysis
2016-06-14
EGAS00001001874
Mutant_clone_mapping_in_normal_oesophagus
Cancer Genomics
2016-06-14
EGAS00001001875
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Other
2016-06-21
EGAS00001001876
Exome and RNA sequencing of relapsed TCF3-PBX1 t(1;19) acute lymphoblastic leukemia
Other
2016-06-19
EGAS00001001878
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Other
2016-06-21
EGAS00001001879
EATL-II STUDY
Other
2016-06-22
EGAS00001001880
Spatiotemporal genomic architecture informs precision oncology in glioblsatoma
Other
2016-06-23
EGAS00001001881
Investigating genetic susceptibility to rheumatic heart disease in Oceania
Other
2016-06-23
EGAS00001001882
Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends
Other
2016-06-24
EGAS00001001883
Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement
Population Genomics
2016-06-27
EGAS00001001886
We performed an integrative analysis to determine genomic aberrations common to sporadic schwannomas.
Other
2016-06-28
EGAS00001001889
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Other
2016-06-30
EGAS00001001891
ORCADES_15x
Whole Genome Sequencing
2016-07-04
EGAS00001001892
Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Other
2016-07-04
EGAS00001001893
The molecular landscape of colorectal cancer reveals genetic mutations.
Other
2016-07-06
EGAS00001001895
Genetic control of the transcriptomic response of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Other
2016-07-06
EGAS00001001896
Molecular dissection of germline chromothripsis in a developmental context
Other
2016-07-07
EGAS00001001897
Integrated Molecular Profilting in Advanced Cancers Trial
Other
2016-07-07
EGAS00001001898
The Prediction and Prevention of Preeclampsia
Other
2016-07-08
EGAS00001001899
Knee_OA_Functional_Genomics
Transcriptome Analysis
2016-07-11
EGAS00001001900
Comparison of EGF and PDGF driven glioblastomas.
Other
2016-07-12
EGAS00001001901
Whole Genome Sequencing of Gingivo-buccal Cancer: ICGC-India Project_YR03
Other
2016-07-13
EGAS00001001906
SNU_WGS_AML
Other
2016-07-18
EGAS00001001908
Breast Cancer - Very young women
Other
2016-07-19
EGAS00001001909
Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies
Other
2016-07-20
EGAS00001001910
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Other
2016-07-24
EGAS00001001911
Lineage-specific genome architecture links disease variants to target genes
Other
2016-07-24
EGAS00001001913
Breast Cancer PDTX Encyclopaedia
Other
2016-07-24
EGAS00001001914
Maastricht IBS cohort MIBS
Other
2016-07-27
EGAS00001001916
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Other
2016-07-30
EGAS00001001918
RNA sequencing in blood samples of cluster headache patients
Other
2016-08-02
EGAS00001001922
DNA methylation and the adverse metabolic outcomes of adiposity
Other
2016-08-02
EGAS00001001923
Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
Other
2016-08-06
EGAS00001001924
MIBS MGS
Other
2016-08-04
EGAS00001001926
Mesenchymal inflammation drives genotoxic stress in hematopoietic stem cells and predicts disease evolution in human pre-leukemia
Other
2016-08-06
EGAS00001001930
Hi-C dataset for testicular germ cell tumour GWAS risk loci, as described in the Oncoarray Litchfield et al. 2016 paper.
Other
2016-08-09
EGAS00001001933
Mutant_clone_mapping_in_normal_oesohagus_and_skin
Other
2016-08-09
EGAS00001001934
Genomic characterization of NUT midline carcinoma
Other
2016-08-09
EGAS00001001937
IHEC DEEP Release August 2016
Other
2016-08-12
EGAS00001001940
Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Other
2016-08-15
EGAS00001001941
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_
Cancer Genomics
2016-08-18
EGAS00001001943
Histone Acetylome-wide Association Study of Autism Spectrum Disorder
Other
2016-08-24
EGAS00001001945
Single cell Transcriptomic Analysis of Cellular Heterogeneity in Human Colorectal Tumors
Other
2016-08-25
EGAS00001001946
CRC Promoter capture Hi-C
Other
2016-08-26
EGAS00001001948
Exome sequencing of samples taken at multipl time points to monitor therapy response in AML
Other
2016-09-01
EGAS00001001949
Targeted sequencing analysis for MDS with HSCT
Other
2016-09-01
EGAS00001001950
Mutational landscape of renal cell carcinoma with venous tumor thrombus
Other
2016-09-01
EGAS00001001951
Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer
Other
2016-09-05
EGAS00001001952
Genomic Analyses Identify Recurrent MEF2D Fusions in Acute Lymphoblastic Leukemia
Other
2016-09-06
EGAS00001001953
Comprehensive molecular profiling identifies novel genetic drivers and subtypes underlying medulloblastoma
Other
2016-09-06
EGAS00001001954
Genomics of enteropathy associated T cell lymphoma (EATL)
Other
2016-09-06
EGAS00001001957
Relaxed selection during a recent human expansion
Other
2016-09-09
EGAS00001001959
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Other
2016-09-12
EGAS00001001960
Novel CNV contribution to schizophrenia from a genome wide study of 41,321 subjects
Other
2016-09-13
EGAS00001001961
Chromosome contacts in activated T cells identify autoimmune disease-candidate genes
Other
2016-09-13
EGAS00001001963
CLL_targeted_exome_sequencing
Cancer Genomics
2016-09-13
EGAS00001001964
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Cancer Genomics
2016-09-14
EGAS00001001967
FFPE_whole_genome_pilot
Cancer Genomics
2016-09-15
EGAS00001001968
Metastatic_Breast_Cancer_Validation
Cancer Genomics
2016-09-15
EGAS00001001969
Whole genome sequencing of colon organoid cultures with artificially induced oncogenic mutations
Other
2016-09-16
EGAS00001001971
In_Situ_Transcription_whole_genome_sequencing
Cancer Genomics
2016-09-20
EGAS00001001972
Breast_Heterogeneity_Validation
Cancer Genomics
2016-09-20
EGAS00001001973
Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Other
2016-09-20
EGAS00001001974
HipSci___Whole_Exome_sequencing___Alport
Other
2016-09-20
EGAS00001001975
HipSci___Whole_Exome_sequencing___Battens
Other
2016-09-20
EGAS00001001976
HipSci___Whole_Exome_sequencing___BPD
Other
2016-09-20
EGAS00001001977
HipSci___Whole_Exome_sequencing___Congenital_hyperinsulinia
Other
2016-09-20
EGAS00001001978
HipSci___Whole_Exome_sequencing___Ataxia
Other
2016-09-20
EGAS00001001979
HipSci___Whole_Exome_sequencing___HSP
Other
2016-09-20
EGAS00001001980
HipSci___Whole_Exome_sequencing___Cardiomyopathy
Other
2016-09-20
EGAS00001001981
HipSci___Whole_Exome_sequencing___Kabuki
Other
2016-09-20
EGAS00001001982
HipSci___Whole_Exome_sequencing___Macular_dystrophy
Other
2016-09-20
EGAS00001001983
HipSci___Whole_Exome_sequencing___PID
Other
2016-09-20
EGAS00001001984
HipSci___Whole_Exome_sequencing___Retinitis_Pigmentosa
Other
2016-09-20
EGAS00001001985
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Other
2016-09-20
EGAS00001001986
HipSci_RNASEQ_Alport
Transcriptome Analysis
2016-09-20
EGAS00001001987
HipSci_RNASEQ_Battens
Transcriptome Analysis
2016-09-20
EGAS00001001988
HipSci_RNASEQ_Congenital_hyperinsulinia
Transcriptome Analysis
2016-09-20
EGAS00001001989
HipSci_RNASEQ_Kabuki
Transcriptome Analysis
2016-09-20
EGAS00001001990
HipSci_RNASEQ_PID
Transcriptome Analysis
2016-09-20
EGAS00001001991
HipSci_RNASEQ_Spastic_paraplegia
Transcriptome Analysis
2016-09-20
EGAS00001001992
HipSci_RNASEQ_Ataxia
Transcriptome Analysis
2016-09-20
EGAS00001001993
HipSci_RNASEQ_BPD
Transcriptome Analysis
2016-09-20
EGAS00001001994
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Transcriptome Analysis
2016-09-20
EGAS00001001995
HipSci_RNASEQ_Macular_Dystrophy
Transcriptome Analysis
2016-09-20
EGAS00001001996
HipSci_RNASEQ_Retinitis_Pigmentosa
Transcriptome Analysis
2016-09-20
EGAS00001001997
HipSci_RNASEQ_Usher syndrome and congenital eye defects
Other
2016-09-20
EGAS00001002005
HipSci HumanExome BeadChip analysis - Hereditary Cerebellar Ataxias
Other
2016-09-23
EGAS00001002006
HipSci HumanExome BeadChip analysis - Hereditary Spastic Paraplegia
Other
2016-09-23
EGAS00001002007
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Other
2016-09-23
EGAS00001002008
HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects
Other
2016-09-23
EGAS00001002009
HipSci HumanExome BeadChip analysis - Alport Syndrome
Other
2016-09-23
EGAS00001002010
HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
Other
2016-09-23
EGAS00001002011
HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy
Other
2016-09-23
EGAS00001002012
HipSci HumanExome BeadChip analysis - Primary immune deficiency
Other
2016-09-23
EGAS00001002013
HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders
Other
2016-09-23
EGAS00001002014
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Other
2016-09-23
EGAS00001002015
HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa
Other
2016-09-23
EGAS00001002016
HipSci HumanExome BeadChip analysis - Battens disease
Other
2016-09-23
EGAS00001002020
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Cerebellar Ataxias
Other
2016-09-23
EGAS00001002021
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Other
2016-09-23
EGAS00001002022
HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Other
2016-09-23
EGAS00001002023
HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
Other
2016-09-23
EGAS00001002024
HipSci HumanHT 12 Expression BeadChip analysis - Alport syndrome
Other
2016-09-23
EGAS00001002025
HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
Other
2016-09-23
EGAS00001002026
HipSci HumanHT 12 Expression BeadChip analysis - Hypertrophic Cardiomyopathy
Other
2016-09-23
EGAS00001002027
HipSci HumanHT 12 Expression BeadChip analysis - Primary immune deficiency
Other
2016-09-23
EGAS00001002028
HipSci HumanHT 12 Expression BeadChip analysis - Bleeding and Platelet disorders
Other
2016-09-23
EGAS00001002029
HipSci HumanHT 12 Expression BeadChip analysis - Macular Dystrophy
Other
2016-09-23
EGAS00001002030
HipSci HumanHT 12 Expression BeadChip analysis - Retinitis Pigmentosa
Other
2016-09-23
EGAS00001002031
HipSci HumanHT 12 Expression BeadChip analysis - Battens disease
Other
2016-09-23
EGAS00001002049
Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium
Other
2016-09-27
EGAS00001002050
WES used for direct identification of clinically relevant neoepitopes presented on native human melanoma tissue by mass spectrometry
Other
2016-09-27
EGAS00001002052
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Other
2016-09-29
EGAS00001002057
Characterization_of_genomic_landscape_of_Peripheral_T_cell_Lymphomas__not_otherwise_specified__PTCL_NOS_
Cancer Genomics
2016-09-30
EGAS00001002059
Exome_sequencing_of_a_cohort_of_Rett_syndromelike_patients
Other
2016-10-03
EGAS00001002060
A_compendium_of_mutational_signatures_due_to_environmental_exposures
Whole Genome Sequencing
2016-10-03
EGAS00001002064
Identification_of_genes_involved_in_congenital_disorders_of_glycosylation_and_3_methylglutaconic_aciduria
Other
2016-10-03
EGAS00001002065
Similarity and diversity of the tumor microenvironment in multiple metastases: critical implications for overall and progression-free survival of high-grade serous ovarian cancer.
Other
2016-10-03
EGAS00001002067
Whole_exome_sequencing_for_clarification_of_rare_causes_of_axonal_Charcot_Marie_Tooth_disease_
Other
2016-10-04
EGAS00001002068
Molecular_diagnosis_of_albinism
Other
2016-10-04
EGAS00001002069
MYOSEQ project
Other
2016-10-05
EGAS00001002070
BLUEPRINT Hematopoietic Stem/Progenitor Cell Methylomes
Epigenetics
2016-10-06
EGAS00001002072
Single-cell RNA sequencing on 5063 single T cells isolated from peripheral blood, tumour and adjacent normal tissues from six hepatocellular carcinoma patients.
Other
2016-10-07
EGAS00001002073
Combining transcription factor binding affinities with open chromatin data for accurate gene expression prediction
Other
2016-10-10
EGAS00001002074
Gene_Characterization_in_Carbohydrate_metabolic_alterations__neonatel_diabetes___congenital_hyperinsulinemic__in_early_childhood
Other
2016-10-10
EGAS00001002075
A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi
Other
2016-10-10
EGAS00001002078
Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Other
2016-10-12
EGAS00001002081
Sequencing_melanoma_germlines
Other
2016-10-13
EGAS00001002082
T19_Chad_xten
Whole Genome Sequencing
2016-10-14
EGAS00001002083
T19_Yemen
Whole Genome Sequencing
2016-10-14
EGAS00001002084
Lebanon_LowCov_seq
Whole Genome Sequencing
2016-10-14
EGAS00001002085
Lebanon_HighCov_seq
Whole Genome Sequencing
2016-10-14
EGAS00001002091
A new subgroup of hepatocellular adenomas with sonic hedgehog pathway activation
Other
2016-10-14
EGAS00001002092
The ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge
Other
2016-10-17
EGAS00001002093
Transcriptional and functional profiling defines human small intestinal macrophage subsets
Other
2016-10-19
EGAS00001002094
Genomic and Epigenomic Features of Primary and Recurrent Hepatocellular Carcinomas
Other
2016-10-19
EGAS00001002100
The Asian Diversity Project: genotyping of 37 Asian populations and ethnic groups
Other
2016-10-22
EGAS00001002102
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Other
2016-10-24
EGAS00001002104
Psoriatic_arthritis
Cancer Genomics
2016-10-25
EGAS00001002105
RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the SardiNIA cohort.
Other
2016-10-26
EGAS00001002106
Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Other
2016-10-28
EGAS00001002107
Melanoma_brain_metastases
Cancer Genomics
2016-10-28
EGAS00001002108
De novo assembly of 150 Danish genomes reveals rich structural complexity
Other
2016-10-31
EGAS00001002110
North American Brain Expression Consortium (NABEC) Exome Sequencing
Other
2016-10-31
EGAS00001002111
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Other
2016-11-01
EGAS00001002113
Exome sequencing of United Kingdom Brain Expression Consortium samples
Other
2016-11-02
EGAS00001002114
Patients with metastatic urothelial carcinoma
Other
2016-11-02
EGAS00001002115
MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition
Other
2016-11-02
EGAS00001002117
Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library
Cancer Genomics
2016-11-08
EGAS00001002123
Meta-analysis of Genome-Wide-Association Sudies for plasma Factor XI
Other
2016-11-09
EGAS00001002124
FFPE_normals_v2_gbm_wtsi_panel
Cancer Genomics
2016-11-09
EGAS00001002128
Preclinical_evolution_of_haematological_malignancies_
Cancer Genomics
2016-11-09
EGAS00001002132
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Cancer Genomics
2016-11-09
EGAS00001002147
Genome-wide association study of prognosis in Crohn's disease
Other
2016-11-11
EGAS00001002149
RNA-sequencing of six Pilocytic astrocytoma tumors
Other
2016-11-14
EGAS00001002150
Inter and intra - tumor heterogeneity in Colorectal Cancer
Other
2016-11-15
EGAS00001002153
The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program 'CASCADE'
Other
2016-11-17
EGAS00001002154
SNU_PROSPECTIVE
Other
2016-11-17
EGAS00001002156
Whole exome sequencing of Parkinson's disease patients from the United Kingdom
Other
2016-11-18
EGAS00001002157
Resequencing_candidate_genes_for_male_spermatogenic_impairment
Resequencing
2016-11-21
EGAS00001002158
A living biobank of breast cancer organoids captures disease heterogeneity
Other
2016-11-21
EGAS00001002159
Assessment of de novo copy number variations in Italian patients with schizophrenia.
Other
2016-11-21
EGAS00001002161
Methylation of Ewing sarcoma tumors (ICGC)
Other
2016-11-22
EGAS00001002164
The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma
Other
2016-11-25
EGAS00001002165
Somatic_mutation_in_skin_epidermis__SMS_
Other
2016-11-25
EGAS00001002167
Osteosarcoma_X10
Cancer Genomics
2016-11-25
EGAS00001002168
Longitudinal analysis of treatment induced genomic alterations in gliomas
Other
2016-11-26
EGAS00001002169
MeDALL epigenetics study
Other
2016-11-28
EGAS00001002170
Scalable whole-genome single-cell library preparation without pre-amplification
Other
2016-11-28
EGAS00001002171
Orphan_Tumour_Study___familial_neuroblastoma
Other
2016-11-29
EGAS00001002173
Prebiotic inulin-type fructans induce specific changes in the human gut microbiota
Other
2016-12-01
EGAS00001002174
The molecular landscape of colorectal cancer (17 cases)
Other
2016-12-02
EGAS00001002175
Genomic and transcriptomic profiling of signalling networks in follicular lymphoma
Other
2016-12-04
EGAS00001002176
The aim of this project is to identify, on 15 French Caucasian and 10 African-Caribbean men, through an integrative approach of DNA sequencing and transciptomic analyses, relevant genomic events that characterize or allow targeting the various phenotypes of aggressiveness of early stages of prostate cancer.
Other
2016-12-05
EGAS00001002182
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Other
2016-12-06
EGAS00001002183
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Other
2016-12-08
EGAS00001002184
miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Other
2016-12-08
EGAS00001002185
Single-cell profiling maps the spectrum of crosstalk between glioma cells and tumor associated macrophages
Other
2016-12-08
EGAS00001002186
Sequencing of pancreatic cancer primary tumors and metastases
Other
2016-12-09
EGAS00001002189
Gene fusion and transcriptomic landscapes of sarcomas
Other
2016-12-14
EGAS00001002190
Widespread DNA hypomethylation and differential gene expression in Turner syndrome
Other
2016-12-14
EGAS00001002192
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Other
2016-12-16
EGAS00001002193
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Other
2016-12-19
EGAS00001002195
Transcriptional mechanisms of resistance to anti-PD-1 therapy
Other
2016-12-20
EGAS00001002197
Oncogenic gene fusions in primary colon cancers
Other
2016-12-21
EGAS00001002198
The genomic landscape of Burkitt Lymphoma
Other
2016-12-22
EGAS00001002199
The genomic landscape of follicular and diffuse large B-cell lymphoma
Other
2016-12-22
EGAS00001002200
Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency
Other
2016-12-27
EGAS00001002201
THAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development
Other
2016-12-31
EGAS00001002202
Genomic Landscape of Pediatric Myelodysplastic Syndromes
Other
2017-01-03
EGAS00001002204
The_identification_of_genetic_vulnerabilities_in_head_and_neck_cancers_for_the_development_of_novel_therapies
Cancer Genomics
2017-01-05
EGAS00001002205
Genomic data from analysis of the human placenta, part of the Pregnancy Outcome Prediction study (POPs)
Other
2017-01-05
EGAS00001002206
Spectrum and significance of MYC and BCL2 mutations in DLBCL
Other
2017-01-06
EGAS00001002207
Circumventing intratumoral heterogeneity to identify potential therapeutic targets in hepatocellular carcinoma. Details please contact lifuqiang@genomics and zhaoxin@genomics.cn.
Other
2017-01-09
EGAS00001002210
Targeted_sequencing_of_blood_DNA_from_Human_twins_
Other
2017-01-09
EGAS00001002211
CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA
Other
2017-01-09
EGAS00001002212
Whole-genome low pass sequencing of 3,514 Sardinian individuals
Other
2017-01-10
EGAS00001002213
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Other
2017-01-10
EGAS00001002216
Warm_autopsy__mutational_signatures_and_clonal_units
Other
2017-01-11
EGAS00001002217
Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Other
2017-01-11
EGAS00001002218
The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Other
2017-01-12
EGAS00001002221
Organoid_Derivation_Project__TGS
Cancer Genomics
2017-01-12
EGAS00001002222
Organoid_Derivation_Project__WGS
Cancer Genomics
2017-01-12
EGAS00001002223
Organoid_Derivation_Pilot__RNAseq
Cancer Genomics
2017-01-12
EGAS00001002224
DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Other
2017-01-12
EGAS00001002225
Tracing the origins of relapse in AML to stem cells
Other
2017-01-12
EGAS00001002226
Aging and genome-wide patterns of DNA methylation in an African rainforest hunter-gathering population
Other
2017-01-13
EGAS00001002228
Identification of fungal species in brain tissue from Alzheimer's disease
Other
2017-01-16
EGAS00001002230
Whole genome bisulfite sequencing of hepatitis B virus-associated hepatocellular carcinoma tumor and non-cancerous samples
Other
2017-01-17
EGAS00001002234
Global Anaplastic Thyroid Cancer Initiative
Other
2017-01-17
EGAS00001002236
Genetics_of_gene_expression_in_human_macrophage_response_to_Salmonella
Transcriptome Analysis
2017-01-18
EGAS00001002237
Sequencing of liver cancer cell lines
Other
2017-01-19
EGAS00001002238
IBD_Whole_Genome_Sequencing
Whole Genome Sequencing
2017-01-19
EGAS00001002239
Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities
Other
2017-01-20
EGAS00001002246
Indonesian sea-nomads genomic history
Other
2017-01-26
EGAS00001002247
TRACERx 100: whole exome data of the first 100 TRACERx tumours
Other
2017-01-30
EGAS00001002248
Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls
Other
2017-01-30
EGAS00001002249
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Other
2017-01-30
EGAS00001002251
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Other
2017-01-30
EGAS00001002253
Genetic_vulnerability_of_knockout_cancer_lines
Other
2017-01-31
EGAS00001002255
Functional_genomics_approaches_to_understand_osteoarthritis
Transcriptome Analysis
2017-01-31
EGAS00001002256
A Functional Network of Gastric-Cancer-Associated Splicing Events Controlled by Dysregulated Splicing Factors
Other
2017-02-01
EGAS00001002257
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Cancer Genomics
2017-02-01
EGAS00001002259
The_impact_of_the_human_leukaemia_virus_HTLV_1_on_host_gene_expression
Whole Genome Sequencing
2017-02-02
EGAS00001002261
CELM
Cancer Genomics
2017-02-02
EGAS00001002262
TSG_knock_out_in_hiPSCs
Cancer Genomics
2017-02-02
EGAS00001002265
Regions of common inter-individual DNA methylation differences in human monocytes.
Other
2017-02-03
EGAS00001002270
Genomic profiling of Acute Lymphoblastic Leukemia in Ataxia Telangiectasia patients reveals tight link between ATM mutations and chromothripsis
Other
2017-02-07
EGAS00001002271
Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Other
2017-02-07
EGAS00001002272
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Other
2017-02-08
EGAS00001002273
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Other
2017-02-08
EGAS00001002274
WGS_of_AML_during_PARPi_therapy
Cancer Genomics
2017-02-08
EGAS00001002275
Whole-genome Sequencing Suggests Mechanisms for 22q11.2 deletion-associated Parkinson’s disease
Other
2017-02-08
EGAS00001002276
GWAS data (Illumina 2.5 M SNPs) in Cuban cohorts of dengue disease
Other
2017-02-08
EGAS00001002278
Single_Cell_RNAseq_at_various_stages_of_HiPSCs_differentiating_toward_definitive_endoderm_and_endoderm_derived_lineages
Transcriptome Analysis
2017-02-09
EGAS00001002294
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Other
2017-02-11
EGAS00001002298
BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs
Other
2017-02-14
EGAS00001002299
Mesothelioma Genomics Study - WGS tumour/normal pairs
Other
2017-02-14
EGAS00001002300
LICA-CN project - 116 liver cancer cases
Other
2017-02-14
EGAS00001002301
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Other
2017-02-14
EGAS00001002305
The Ovarian Cancer Association Consortium OncoArray genome-wide association study
Other
2017-02-14
EGAS00001002306
Whole-Genome Sequencing of a Healthy Aging Cohort.
Other
2017-02-14
EGAS00001002309
Next_gen_seq_of_eye_cancers
Cancer Genomics
2017-02-15
EGAS00001002312
Whole-exome sequencing of PTC, benign nodule and normal tissues in 28 patients
Other
2017-02-16
EGAS00001002314
Sequencing of paediatric High Grade Gliomas and DIPG
Other
2017-02-21
EGAS00001002317
18 Whole Exome Sequencing for Radiation Induced-Meningiomas
Other
2017-02-21
EGAS00001002318
RNA seq on 19 samples of Radiation-Induced Meningiomas
Other
2017-02-21
EGAS00001002319
Whole exome sequencing in RVOT patients
Other
2017-02-22
EGAS00001002320
Massively parallel nanowell-based single-cell gene expression profiling
Other
2017-02-22
EGAS00001002322
Functional_genomics_approaches_to_understand_osteoarthritis
Population Genomics
2017-02-23
EGAS00001002323
The Immune Microenvironment, Genome–Wide Copy Number Aberrations and Survival in Mesothelioma
Other
2017-02-23
EGAS00001002324
Genome-to-genome analysis highlights the impact of the human innate and adaptive immune systems on the hepatitis C virus
Other
2017-02-24
EGAS00001002325
Kidney_Single_Cell_Study
Transcriptome Analysis
2017-02-24
EGAS00001002326
Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Other
2017-02-27
EGAS00001002328
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Other
2017-02-27
EGAS00001002329
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Cancer Genomics
2017-02-27
EGAS00001002331
160 WES and 25 WGS for HBV related HCC, and 15 WES for ICC belongs LICA-CN.
Other
2017-03-01
EGAS00001002333
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Other
2017-03-01
EGAS00001002334
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
Other
2017-03-01
EGAS00001002335
Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors.
Other
2017-03-02
EGAS00001002336
UK renal cancer samples genotyped on Illumina OmniExpress BeadChip
Other
2017-03-02
EGAS00001002337
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Other
2017-03-03
EGAS00001002338
whole genome sequence data of multifocal hepatocellular carcinoma
Other
2017-03-03
EGAS00001002340
Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease
Other
2017-03-06
EGAS00001002343
Copy number profiling of putative cancer stem from pleural effusion aspirates from breast cancer patients
Other
2017-03-07
EGAS00001002344
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Other
2017-03-07
EGAS00001002346
Transcriptome sequencing of myelodysplasia
Other
2017-03-09
EGAS00001002347
Edinburgh_Naevi_Cohort
Cancer Genomics
2017-03-09
EGAS00001002352
In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer.
Other
2017-03-10
EGAS00001002364
Ongoing_mutagenesis_RNAseq
Cancer Genomics
2017-03-10
EGAS00001002366
CEHM
Cancer Genomics
2017-03-10
EGAS00001002368
HYPERMUTATION AND MALIGNANT PROGRESSION IN LOW-GRADE GLIOMA PATIENTS
Other
2017-03-10
EGAS00001002372
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_2
Cancer Genomics
2017-03-13
EGAS00001002374
The molecular landscape of colorectal cancer (5 cases)
Other
2017-03-14
EGAS00001002376
Molecular Subtype-specific Biomarkers Improves Colorectal Cancer Prognostication
Other
2017-03-15
EGAS00001002377
Tumor-derived exosomes modulate PD-L1 expression in monocytes
Other
2017-03-15
EGAS00001002379
Somatic_mutations_in_twin_breast_cancers
Cancer Genomics
2017-03-15
EGAS00001002380
Botswana 15 autosomal unlinked microsatellites
Other
2017-03-16
EGAS00001002382
Field_effect_of_healthy_and_diseased_livers
Cancer Genomics
2017-03-16
EGAS00001002388
2017_AML_WGS
Other
2017-03-21
EGAS00001002390
Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Other
2017-03-21
EGAS00001002393
Genomic landscape of oral cancers (Complete Genomics WGS)
Other
2017-03-22
EGAS00001002398
WGS of T-cell and NK-cell lymphoma for ICGC (NKTL-SG)
Other
2017-03-27
EGAS00001002400
Biological insights from the whole genome sequences of human embryonic stem cell lines
Other
2017-03-27
EGAS00001002402
Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population.
Other
2017-03-28
EGAS00001002404
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Other
2017-03-29
EGAS00001002405
Targeted resequencing of ribosomal proteins in multiple myeloma patient samples.
Other
2017-03-29
EGAS00001002406
Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations
Other
2017-03-29
EGAS00001002408
Whole Genome Sequencing of Liver Cancers
Other
2017-03-30
EGAS00001002409
Human_primary_melanoma_project
Other
2017-03-31
EGAS00001002410
Suppressors and activators of JAK-STAT signaling at diagnosis and relapse of acute lymphoblastic leukemia in Down Syndrome
Other
2017-04-01
EGAS00001002413
Field_effect_of_healthy_and_diseased_livers_WGS
Other
2017-04-04
EGAS00001002414
ChIP Seq data of multiple myeloma and plasma cell leukaemia cell lines
Other
2017-04-04
EGAS00001002415
TRACERx 100: metastatic samples
Other
2017-04-05
EGAS00001002416
WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin
Cancer Genomics
2017-04-05
EGAS00001002418
Exome sequencing of pseudomyxoma peritonei
Other
2017-04-07
EGAS00001002419
Clinical and genetic analysis of a rare syndrome associated with neoteny
Other
2017-04-07
EGAS00001002420
Whole genome sequencing identified biomarker of response to PD1 blockade in Natural-killer/T-cell lymphoma
Other
2017-04-10
EGAS00001002421
CD36 defines CML cells less sensitive to imatinib
Other
2017-04-10
EGAS00001002422
The genomic landscape of germinal center derived B-cell lymphomas other than follicular, diffuse-large B-cell and Burkitt lymphom
Other
2017-04-11
EGAS00001002423
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Other
2017-04-11
EGAS00001002424
Cell fate mapping of human glioblastoma reveals an invariant stem cell hierarchy pre- and post-treatment
Other
2017-04-11
EGAS00001002425
Whole Mitochondrial Sequencing of Gingivo-buccal Cancer: ICGC-India Project
Other
2017-04-12
EGAS00001002428
A dataset compiled as a resource a for orthogonal assessment of exon CNV calling in NGS data
Other
2017-04-18
EGAS00001002430
Deep single-cell RNA sequencing data for 12346 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive NSCLC patients
Other
2017-04-19
EGAS00001002431
Neurodegenerative_TGS
Cancer Genomics
2017-04-20
EGAS00001002432
The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Other
2017-04-21
EGAS00001002433
Genomic landscape of Chordoid Glioma
Other
2017-04-24
EGAS00001002436
Subclonal evolution of four ER+ breast cancers determined by WGS and scRNA-Seq
Other
2017-04-25
EGAS00001002437
Integrative genomic and transcriptomic analysis of adult leiomyosarcoma (HIPO-028, HIPO-018, HIPO-021)
Other
2017-04-25
EGAS00001002438
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Transcriptome Analysis
2017-04-26
EGAS00001002439
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Other
2017-04-26
EGAS00001002440
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Other
2017-04-26
EGAS00001002441
Successful immune checkpoint blockade in a patient with advanced stage microsatellite unstable biliary tract cancer (H021)
Other
2017-04-26
EGAS00001002443
Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma
Other
2017-05-02
EGAS00001002444
A combined circulating tumor DNA and protein biomarker-based liquid biopsy for the earlier detection of pancreatic cancer
Other
2017-05-02
EGAS00001002445
Control samples, breast cancer clinical samples and matched patient-derived tumour xenografts (PDTXs) to develop and test a computational approach to discriminate human and mouse sequences in PDTXs
Other
2017-05-03
EGAS00001002449
Integrative single-cell and cell-free plasma RNA transcriptomics elucidates placental cellular dynamics
Other
2017-05-05
EGAS00001002450
Mutations in SPINK2 induce azoospermia
Other
2017-05-05
EGAS00001002452
Whole_genome_sequencing_of_100_DDD_trios_with_suspected_noncoding_causal_mutations
Whole Genome Sequencing
2017-05-08
EGAS00001002453
Comprehensive Molecular Analysis of Colon Cancer for the Identification and Validation of New Biomarkers
Other
2017-05-09
EGAS00001002454
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Other
2017-05-09
EGAS00001002457
The demographic history and mutational load of African hunter-gatherers and farmers
Other
2017-05-10
EGAS00001002460
SNP array data for the Milieu Intérieur cohort
Other
2017-05-12
EGAS00001002461
Whole_Genome_Sequencing_of_INTERVAL
Whole Genome Sequencing
2017-05-12
EGAS00001002462
PCR-free HiSeqX whole genome sequence data on 120 samples with triplet repeat expansions (premutation and full expansions)
Other
2017-05-12
EGAS00001002463
ChIP-seq of GOF p53 mutants
Other
2017-05-13
EGAS00001002471
Mutational_signatures_and_clonal_dynamics_in_normal_human_tissues
Cancer Genomics
2017-05-16
EGAS00001002472
CINECA synthetic data.Please note: This study contains synthetic data (with cohort “participants” / ”subjects” marked with FAKE) has no identifiable data and cannot be used to make any inference about cohort data or results.
Other
2017-05-16
EGAS00001002473
Fungal infection in neural tissue from Amyotrophic Lateral Sclerosis
Other
2017-05-17
EGAS00001002474
Genomic_profiling_of_B_other_Adult_ALL_WGS
Other
2017-05-17
EGAS00001002475
Identification of fusion transcripts by RNA-sequencing and Whole genome sequencing of a METABRIC patient sample
Other
2017-05-18
EGAS00001002477
GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER
Other
2017-05-18
EGAS00001002478
Cell motility and migration as determinants of stem cell efficacy
Other
2017-05-18
EGAS00001002479
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Other
2017-05-22
EGAS00001002481
CNV detection in targeted NGS panel data
Other
2017-05-23
EGAS00001002482
H3Africa - Genomic and Environmental Risk Factors for Cardiometabolic Disease in Africans
Other
2017-05-24
EGAS00001002483
Hip OA Functional Genomics
Transcriptome Analysis
2017-05-24
EGAS00001002484
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Other
2017-05-25
EGAS00001002485
Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment
Other
2017-05-26
EGAS00001002486
Kidney_tumour_DNA
Cancer Genomics
2017-05-26
EGAS00001002487
Kidney_tumour_RNA
Cancer Genomics
2017-05-26
EGAS00001002489
Paediatric IBD Mosaicism
Other
2017-05-26
EGAS00001002490
Mutational signatures of aflatoxin
Other
2017-05-29
EGAS00001002492
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Other
2017-05-31
EGAS00001002493
Whole_Exome_PC9_and_A375
Cancer Genomics
2017-06-01
EGAS00001002494
Profiling_molecular_heterogeneity_in_human_primary_microglia
Transcriptome Analysis
2017-06-01
EGAS00001002495
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Other
2017-06-04
EGAS00001002496
H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples
Other
2017-06-05
EGAS00001002499
Genetic Risk for Subsequent Neoplasms among Long-term Survivors of Childhood Cancer in the St. Jude Lifetime Cohort
Other
2017-06-06
EGAS00001002501
Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Other
2017-06-09
EGAS00001002504
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Other
2017-06-09
EGAS00001002505
H3K27ac and RNA-seq data of neuroblastoma PDXs and/or primary tumors
Other
2017-06-12
EGAS00001002506
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie
Other
2017-06-12
EGAS00001002507
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Other
2017-06-12
EGAS00001002508
Fibroblast heterogeneity and immunosuppressive environment in Human breast cancer
Other
2017-06-13
EGAS00001002509
Combination Therapies for Personalised Cancer Medicine in drug resistant EGFR mutant lung cancer
Other
2017-06-14
EGAS00001002511
Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Other
2017-06-14
EGAS00001002512
Mutation_burden_in_sun_exposed_eyelid__MSSE_
Other
2017-06-15
EGAS00001002515
Pharmacogenomic landscape of patient-derived cells informs precision oncology therapy
Other
2017-06-16
EGAS00001002517
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Other
2017-06-19
EGAS00001002518
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Other
2017-06-20
EGAS00001002520
Local In Time Statistics for processual research
Other
2017-06-21
EGAS00001002521
Cylindromas_sun_protected_and_exposed
Cancer Genomics
2017-06-21
EGAS00001002523
Genome_Diversity_in_Africa_Project__Uganda
Whole Genome Sequencing
2017-06-21
EGAS00001002526
The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Other
2017-06-21
EGAS00001002527
Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study
Other
2017-06-21
EGAS00001002528
Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors
Other
2017-06-21
EGAS00001002533
Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Other
2017-06-23
EGAS00001002534
Orphan_Tumour_Study___RNAseq
Cancer Genomics
2017-06-23
EGAS00001002535
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Other
2017-06-26
EGAS00001002536
A biobank of patient-derived pediatric brain tumor models
Other
2017-06-27
EGAS00001002537
Integrative genomic analysis identifies multiple subtypes and therapeutic targets in acute erythroid leukemia
Other
2017-06-27
EGAS00001002538
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Other
2017-06-27
EGAS00001002543
PanCuRx Translational Research Initiative
Other
2017-06-28
EGAS00001002549
Genomic landscape of human diversity across Madagascar
Other
2017-07-04
EGAS00001002551
Y_chromosome_mis_segregation_in_the_DLD_1_cell_line
Cancer Genomics
2017-07-06
EGAS00001002553
Pilot_Fetal_Cell_Atlas_RNAseq
Transcriptome Analysis
2017-07-07
EGAS00001002554
Genentech - Cell line exome sequencing
Other
2017-07-07
EGAS00001002555
Plasma pQTLs in INTERVAL cohort
Other
2017-07-10
EGAS00001002556
TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells.
Other
2017-07-10
EGAS00001002557
Copy-number signatures and mutational processes in ovarian carcinoma
Other
2017-07-10
EGAS00001002558
Genomic diversity of the African-descent Makranis of Pakistan
Other
2017-07-11
EGAS00001002559
Exome-wide somatic mutation characterization of small bowel adenocarcinoma
Other
2017-07-11
EGAS00001002560
Single-cell RNA sequencing reveals cell-type specific eQTLs in peripheral blood mononuclear cells
Other
2017-07-11
EGAS00001002562
Exome sequencing data from two myelosarcomas
Other
2017-07-11
EGAS00001002565
Genetic history of the Comorian populations.
Other
2017-07-12
EGAS00001002566
Combined clinical and gene expression score identifies high-risk individuals among follicular lymphoma patients on immunotherapy
Other
2017-07-13
EGAS00001002567
Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples
Other
2017-07-13
EGAS00001002568
KLB mutations in congenital hypogonadotropic hypogonadism
Other
2017-07-13
EGAS00001002569
Genetic history of the Swahili population
Other
2017-07-13
EGAS00001002570
Progression to AML is predictable and distinct from age related clonal hematopoiesis
Other
2017-07-13
EGAS00001002571
Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks
Other
2017-07-17
EGAS00001002576
Comparative genomics research for Chinese colorectal cancer
Other
2017-07-19
EGAS00001002577
Direct Detection of Early-stage Cancers Using Circulating Tumor DNA
Other
2017-07-19
EGAS00001002578
Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma
Other
2017-07-20
EGAS00001002579
Combination Therapies for Personalised Cancer Medicine in 11-18
Other
2017-07-20
EGAS00001002581
Molecular profiling of MBD4-deficient acute myeloid leukaemia
Other
2017-07-21
EGAS00001002582
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Other
2017-07-21
EGAS00001002586
Transcriptome analysis in very preterm infants with chronic lung disease after birth
Other
2017-07-24
EGAS00001002588
Systematic kinase inhibitor profiling identifies CDK9 as a synthetic lethal target in NUT midline carcinoma
Other
2017-07-25
EGAS00001002589
High Grade Serous Ovarian Carcinomas Originate in the Fallopian Tube
Other
2017-07-25
EGAS00001002591
Genes associated with pancreas development and function maintain open chromatin in iPSCs generated from human pancreatic beta cells
Other
2017-07-25
EGAS00001002592
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Other
2017-07-25
EGAS00001002593
Illumina HiSeqX whole genome sequence data on 58 samples including 54 with known HTT triplet repeat expansions (2 premutation and 52 full expansions)
Other
2017-07-25
EGAS00001002594
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Other
2017-07-26
EGAS00001002597
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Other
2017-08-01
EGAS00001002598
Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Other
2017-08-01
EGAS00001002599
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Epigenetics
2017-08-02
EGAS00001002602
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Other
2017-08-02
EGAS00001002604
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Other
2017-08-03
EGAS00001002605
The chromatin accessibility signature of human immune aging stems from CD8+ T cells
Other
2017-08-03
EGAS00001002606
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Other
2017-08-03
EGAS00001002607
Comparative genomics research for Chinese colorectal cancer
Other
2017-08-07
EGAS00001002608
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Cancer Genomics
2017-08-07
EGAS00001002609
Reduced Representation Bisulfite Sequencing (RRBS) in various tissues to discover DNA methylation markers for the diagnosis of breast and ovarian cancer.
Other
2017-08-08
EGAS00001002610
Somatic_Variation_Angiosarcoma
Cancer Genomics
2017-08-09
EGAS00001002612
The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure
Other
2017-08-09
EGAS00001002614
Capture Hi-C on MM
Other
2017-08-11
EGAS00001002616
Breast cancer women lack normal lifelong immune response after full-term pregnancies
Other
2017-08-14
EGAS00001002617
AngioPredict CNV and Exome data
Other
2017-08-14
EGAS00001002618
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH
Epigenetics
2017-08-14
EGAS00001002619
Cryptic Relatedness in the Singapore Living Biobank Project
Other
2017-08-15
EGAS00001002621
Multi-omics Profiling of Asian Breast Cancers
Other
2017-08-16
EGAS00001002622
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping
Other
2017-08-16
EGAS00001002624
The_genetics_of_thinness_compared_to_obesity
Population Genomics
2017-08-18
EGAS00001002625
Clonal evolution study of Intrahepatic cholangiocarcinoma in Zhongshan Hospital
Other
2017-08-20
EGAS00001002626
Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS
Cancer Genomics
2017-08-22
EGAS00001002627
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Other
2017-08-22
EGAS00001002628
2017_prospective_v2 Whole Exome Sequencing
Other
2017-08-28
EGAS00001002630
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1).
Other
2017-08-28
EGAS00001002631
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples
Other
2017-08-29
EGAS00001002632
Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
Other
2017-08-30
EGAS00001002633
_Isotype_resolved_sequencing_of_B_cell_receptor__in_sorted_memory_populations
Transcriptome Analysis
2017-08-30
EGAS00001002634
Isotype_resolved_sequencing_of_B_cell_receptor__in_health_and_disease
Transcriptome Analysis
2017-08-30
EGAS00001002635
Isotype_resolved_sequencing_of_B_cell_receptor_in_measles_virus_infection
Transcriptome Analysis
2017-08-30
EGAS00001002636
Cross-tissue transcriptomic analysis of human secondary lymphoid organ residing ILC3 reveals a default quiescent state in the absence of inflammation
Other
2017-08-30
EGAS00001002637
HDAC inhibitors in synovial sarcoma cells
Other
2017-08-30
EGAS00001002639
The Southern African Human Genome Programme
Other
2017-09-04
EGAS00001002641
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Other
2017-09-06
EGAS00001002642
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Transcriptome Analysis
2017-09-07
EGAS00001002643
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Population Genomics
2017-09-07
EGAS00001002645
Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors
Other
2017-09-08
EGAS00001002646
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Other
2017-09-08
EGAS00001002649
Transcriptional_analysis_of_cells_from_lungs
Cancer Genomics
2017-09-11
EGAS00001002650
Ultra-fast multiplex small DNA sequencing on the MinION nanopore sequencing platform
Other
2017-09-12
EGAS00001002652
Childhood_arthritis_DNA
Cancer Genomics
2017-09-13
EGAS00001002654
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Other
2017-09-13
EGAS00001002655
DEEP IHEC release 2017
Other
2017-09-13
EGAS00001002656
H3Africa - Collaborative African Genomics Network
Other
2017-09-14
EGAS00001002657
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Other
2017-09-15
EGAS00001002658
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WGS
Cancer Genomics
2017-09-15
EGAS00001002659
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_TGS
Cancer Genomics
2017-09-15
EGAS00001002660
RNA sequencing data of 66 matched primary and recurrent high grade serous ovarian cancer
Other
2017-09-15
EGAS00001002662
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Other
2017-09-18
EGAS00001002664
Exome_trios_in_patients_with_gastroschisis
Other
2017-09-19
EGAS00001002665
Family-based GWAS for CRSwNP
Other
2017-09-19
EGAS00001002667
Immunodeficiency_
Other
2017-09-20
EGAS00001002668
WGS of 32 paired SRCC samples
Other
2017-09-22
EGAS00001002670
We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Other
2017-09-26
EGAS00001002671
MicroRNA expression in malignant and benign breast tissue – the Norwegian Women and Cancer study
Other
2017-09-26
EGAS00001002674
Y_phylogeny_haplogroupDE
Resequencing
2017-09-28
EGAS00001002676
Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Other
2017-09-28
EGAS00001002678
Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Other
2017-09-29
EGAS00001002679
Employing_single_cell_sequencing_for_detection_of_mutational_signatures_reflecting_on_going_mutagenesis_
Cancer Genomics
2017-09-29
EGAS00001002680
WGS___Exploration_of__mutational_processes_in_human_cancer_cell_lines
Cancer Genomics
2017-09-29
EGAS00001002681
Genome-wide mutational consequences of nucleotide excision repair-deficiency through XPC deletion in a human adult stem cell culture
Other
2017-10-02
EGAS00001002682
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Other
2017-10-03
EGAS00001002684
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Other
2017-10-04
EGAS00001002685
WGS of breast cancer diagnosed during pregnancy and matched control
Other
2017-10-05
EGAS00001002687
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Other
2017-10-06
EGAS00001002692
Wilms_Tumour_organoid_sequencing_WGS
Cancer Genomics
2017-10-06
EGAS00001002694
MMR (DNA mismatch repair) pathway in human samples
Other
2017-10-06
EGAS00001002696
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Other
2017-10-10
EGAS00001002697
Alternative splicing isoforms in patient-derived hepatocellular carcinoma cells
Other
2017-10-11
EGAS00001002698
Gut microbiome modulates response to anti PD1 immunotherapy in metastatic melanoma patients
Other
2017-10-11
EGAS00001002699
TCR β-chain repertoire characterization of regulatory and conventional T cells in peripheral blood from breast cancer patients and healthy individuals.
Other
2017-10-12
EGAS00001002700
Genome-wide DNA Methylation is Predictive of Outcome in Juvenile Myelomonocytic Leukemia
Other
2017-10-13
EGAS00001002702
Multi-omics data of 1000 Inflammatory Bowel Disease patients
Other
2017-10-23
EGAS00001002703
The integrated genomic and immune landscapes of lethal metastatic breast cancer.
Other
2017-10-23
EGAS00001002704
Dynamics of neoantigen landscape during immunotherapy
Other
2017-10-23
EGAS00001002705
Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Other
2017-10-25
EGAS00001002707
Sequencing-based counting and size profiling of plasma Epstein-Barr virus DNA enhance population screening of nasopharyngeal carcinoma.
Other
2017-10-27
EGAS00001002708
Targeted_sequencing_of_cylindroma_patients
Other
2017-10-27
EGAS00001002709
Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments
Other
2017-10-28
EGAS00001002714
Keratinocyte_CRISPR_screens
Cancer Genomics
2017-11-02
EGAS00001002717
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Other
2017-11-03
EGAS00001002718
We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy.
Other
2017-11-06
EGAS00001002719
We performed whole-exome sequencing and whole epigenome sequencing (RRBS) of samples collected from different time points during radiotherapy from thirty-four ESCC patients. We compared the genetic and epigenetic features of the different time biopsy samples to reveal the changes in ESCC received radiotherapy.
Other
2017-11-06
EGAS00001002720
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Other
2017-11-06
EGAS00001002721
Characterization of a human iPSC-derived islet differentiation model
Other
2017-11-06
EGAS00001002723
Genetic_Overlap_between_Metabolic_and_Psychiatric_disease
Whole Genome Sequencing
2017-11-09
EGAS00001002724
Angiopredict: predicting response for bevacizumab treatment
Other
2017-11-09
EGAS00001002725
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Cancer Genomics
2017-11-09
EGAS00001002726
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas
Cancer Genomics
2017-11-09
EGAS00001002727
Exome and RNA sequencing of Greenlanders
Other
2017-11-13
EGAS00001002728
CancerDetector: Ultrasensitive and Non-Invasive Cancer Detection at the Resolution of Individual Reads using Cell-free DNA Methylation Sequencing Data
Other
2017-11-15
EGAS00001002729
We describe a method to culture organoids from adult human kidney tissue and describe applications for the culture system.
Other
2017-11-16
EGAS00001002730
Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D)
Other
2017-11-16
EGAS00001002731
Himalayan_population_genetic_study
Population Genomics
2017-11-16
EGAS00001002733
Targeted next-generation sequencing of 13 chordoid gliomas of the third ventricle
Cancer Genomics
2017-11-22
EGAS00001002736
Molecular characterization of endothelial cells under conditions associated with hematopoietic niche formation in humans
Other
2017-11-22
EGAS00001002737
Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data.
Other
2017-11-23
EGAS00001002738
X chromosomal genetic variants are associated with childhood obesity
Other
2017-11-26
EGAS00001002740
Targeted Gene Panel for 171 PTCLs
Other
2017-11-27
EGAS00001002742
The_British_Autozygosity_Populations_BioResource
Other
2017-11-28
EGAS00001002743
Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma
Other
2017-11-29
EGAS00001002744
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Other
2017-11-29
EGAS00001002745
Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients
Other
2017-11-30
EGAS00001002746
BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology)
Other
2017-11-30
EGAS00001002747
Somatic_mutation_and_clonal_evolution_in_premalignant_lung_disease___WGS
Cancer Genomics
2017-12-01
EGAS00001002749
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Epigenetics
2017-12-04
EGAS00001002750
Mitochondrial DNA mutations contribute to autism and also to the characteristics of mitochondrial disorders present in patients with autism spectrum disorders
Other
2017-12-04
EGAS00001002751
Antisense long non-coding RNAs are deregulated in skin tissue of patients with systemic sclerosis
Other
2017-12-04
EGAS00001002753
Defective T-cell expansion in RASGRP1 deficiency
Other
2017-12-04
EGAS00001002754
IBD_Whole_Genome_Sequencing
Whole Genome Sequencing
2017-12-07
EGAS00001002755
The European Bank for Induced Pluripotent stem cells (EBiSC) is designed to address the increasing demand by iPSC researchers for quality-controlled, disease-relevant research grade iPSC lines, data and cell services.In this study Whole Genome Sequencing was performed on a selection of lines from the project.
Other
2017-12-14
EGAS00001002756
GWAS in a dengue Thai cohort
Other
2017-12-14
EGAS00001002757
Aberrant ERBB4-SRC Signaling as a Hallmark of Group 4 Medulloblastoma Revealed by Integrative Phosphoproteomic Profiling
Other
2017-12-14
EGAS00001002758
Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009
Other
2017-12-14
EGAS00001002759
NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Other
2017-12-15
EGAS00001002760
Germline alterations of acute myeloid leukemia
Other
2017-12-15
EGAS00001002761
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Other
2017-12-15
EGAS00001002762
HSC_population_dynamics_KSP_samples
Cancer Genomics
2017-12-15
EGAS00001002763
Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer
Other
2017-12-15
EGAS00001002764
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Other
2017-12-16
EGAS00001002765
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Other
2017-12-18
EGAS00001002766
Co-infection of fungi and bacteria in brain tissue of Alzheimer’s patients.
Other
2017-12-18
EGAS00001002767
The genomic and radiomic complexity of multifocal prostate cancer
Other
2017-12-18
EGAS00001002769
Insular Celtic population structure and genomic footprints of migration
Other
2017-12-18
EGAS00001002770
DSRCT RNA genomic sequencing
Other
2017-12-18
EGAS00001002771
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 2).
Other
2017-12-19
EGAS00001002772
An integrated molecular study of 20 hepatoblastoma pairs using whole genome sequencing and RNA sequencing
Other
2017-12-20
EGAS00001002773
Mutational profiling of LUAD in young never-smokers
Other
2017-12-20
EGAS00001002777
Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Other
2017-12-21
EGAS00001002778
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Other
2017-12-21
EGAS00001002782
Kibbutzim Family study
Other
2017-12-28
EGAS00001002783
Whole-exome sequencing reveals the origin and evolution of Hepato-Cholangiocarcinoma
Other
2018-01-01
EGAS00001002784
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Other
2018-01-02
EGAS00001002786
An Empirical Approach Leveraging Tumorgrafts to Dissect the Tumor Microenvironment in Renal Cell Carcinoma Identifies Missing Link to Prognostic Inflammatory Factors
Other
2018-01-04
EGAS00001002787
Whole_Genome_Sequencing_of_INTERVAL
Other
2018-01-05
EGAS00001002788
Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing.
Other
2018-01-08
EGAS00001002789
CD49f single-cell methylomes
Other
2018-01-09
EGAS00001002790
Preferential infiltration of distinct Vγ9δ2 T cells into Glioblastoma multiforme
Other
2018-01-10
EGAS00001002791
Deep single-cell RNA sequencing data for 11138 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive CRC patients. The DATA ACCESS AGREEMENT is provided at https://github.com/zhangyybio/single-T-cell-data-access. Applicants can request access to the data by directly downloading it or by sending an email to cancerpku@pku.edu.cn. The process that is used to approve an application includes verifying the institution, participants and research purposes of the application. In general this process will take about two weeks. In principal, any scientific research program complying with the laws and bioethic regulation policies of China will be approved.
Other
2018-01-10
EGAS00001002792
Breast cancer DNA repair
Other
2018-01-10
EGAS00001002793
TRACERx Renal 100
Other
2018-01-10
EGAS00001002795
Molecular profiling of acinar cell carcinoma of the salivary glands
Other
2018-01-11
EGAS00001002796
Somatic IL4R Hotspot Mutations in Primary Mediastinal Large B-cell lymphoma lead to constitutive JAK-STAT activation
Other
2018-01-11
EGAS00001002797
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Other
2018-01-12
EGAS00001002798
Hominin-specific NOTCH2 paralogs expand human cortical neurogenesis through regulation of Delta/Notch interactions.
Other
2018-01-15
EGAS00001002801
Analysis of Complex Genomic Rearrangements of Lung Adenocarcinomas
Other
2018-01-16
EGAS00001002802
RNA-seq profiling of NKX6.1 reporter iPSC lines for isolation and analysis of functionally relevant neuronal and pancreas populations
Other
2018-01-16
EGAS00001002803
Sensitive and Frequent Identification of High Avidity Neo-epitope Specific CD8 + T-cells in Immunotherapy-naïve Ovarian Cancer
Other
2018-01-18
EGAS00001002804
2018_ETO_WGS
Other
2018-01-19
EGAS00001002805
Predictor_RIO_TNBC
Cancer Genomics
2018-01-19
EGAS00001002806
Predictor_ChemoNEAR_TNBC
Cancer Genomics
2018-01-19
EGAS00001002807
Genomic profiling of matched well differentiated and de-differentiated liposarcoma.
Other
2018-01-19
EGAS00001002809
Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Other
2018-01-23
EGAS00001002811
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Other
2018-01-23
EGAS00001002812
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Other
2018-01-23
EGAS00001002814
Natural variation of circulating RNAs in human serum
Other
2018-01-24
EGAS00001002816
Prostate Cancer and Normal Adjacent Prostate RNA-seq samples, NGS-ProToCol
Other
2018-01-25
EGAS00001002818
Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes
Other
2018-01-26
EGAS00001002819
2014_AML_WES_51 samples
Other
2018-01-26
EGAS00001002820
Molecular subtypes of malignant peritoneal mesothelioma
Other
2018-01-27
EGAS00001002822
Psoriatic_arthritis_WGS
Cancer Genomics
2018-01-29
EGAS00001002823
Physiological and genetic adaptations to diving in Sea Nomads
Other
2018-01-29
EGAS00001002825
Whole genome and whole exome sequencing of epilaptic patients
Other
2018-01-29
EGAS00001002826
A novel subset of human CD33+ haematopoietic stem cells characterized at single-cell resolution
Other
2018-01-31
EGAS00001002827
Ibrutinib induces a global chromatin reorganisation in chronic lymphocytic leukaemia
Other
2018-01-31
EGAS00001002830
Single cell sequencing reveals the origin and the order of mutation acquisition in T-cell acute lymphoblastic leukemia.
Other
2018-02-05
EGAS00001002831
Size-tagged preferred ends in maternal plasma DNAshed light on the production mechanism and showutility in noninvasive prenatal testing
Other
2018-02-06
EGAS00001002832
Transcriptome profiling of human plucked frontal and occipital hair follicles
Other
2018-02-06
EGAS00001002833
Genomic profiling of ovarian adult type granulosa cell tumors
Other
2018-02-06
EGAS00001002836
DNA methylation using EPIC array in UK population study
Other
2018-02-07
EGAS00001002839
The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Other
2018-02-07
EGAS00001002840
A novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient
Other
2018-02-08
EGAS00001002842
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WES
Cancer Genomics
2018-02-08
EGAS00001002843
Korean Lung Cancer - 36 pair WES data
Other
2018-02-09
EGAS00001002844
2014_Lung_sq_WES
Other
2018-02-09
EGAS00001002845
Single cell sequencing of breast cancer T cells reveals a tissue-resident memory subset associated with improved prognosis
RNASeq
2018-02-12
EGAS00001002846
Whole exome sequencing of longitudinal samples from a melanoma patient receiving MEK plus CDK4/6 inhibitor therapy.
Other
2018-02-12
EGAS00001002847
ALPI deficiency and inflammatory bowel disease
Other
2018-02-13
EGAS00001002850
A genomic approach towards an understanding of clonal evolution and disease progression in multiple myeloma
Other
2018-02-16
EGAS00001002851
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_YR03
Other
2018-02-16
EGAS00001002852
Whole Exome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch04
Other
2018-02-16
EGAS00001002853
Genomic and functional fidelity of small cell lung cancer patient-derived xenografts
Other
2018-02-16
EGAS00001002854
Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol
Other
2018-02-16
EGAS00001002856
Integrated analysis of relapsed B-cell precursor Acute Lymphoblastic Leukemia identifies subtype-specific cytokine and metabolic signatures
Other
2018-02-16
EGAS00001002857
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Other
2018-02-16
EGAS00001002858
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Cancer Genomics
2018-02-16
EGAS00001002859
Targeted panel data for newly diagnosed myeloma patients.
Other
2018-02-16
EGAS00001002860
Whole-genome and transcriptome sequencing of tumor-stage mycosis fungoides
Other
2018-02-19
EGAS00001002861
Investigating_the_impact_of_MBD4_on_the_mutability_of_the_germline
Whole Genome Sequencing
2018-02-20
EGAS00001002863
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Cancer Genomics
2018-02-20
EGAS00001002864
Genome analysis of oesophageal cancer and Barrett's oesophagus
Other
2018-02-20
EGAS00001002865
Human Pancreatic Beta Cell lncRNAs Control Cell-Specific Regulatory Networks
Other
2018-02-21
EGAS00001002866
Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_
Cancer Genomics
2018-02-21
EGAS00001002869
Exome and RNA sequencing data from 32 ocular and extraocular sebaceous carcinomas
Other
2018-02-21
EGAS00001002871
Targeted exome sequencing of pleomorphic invasive lobular carcinoma (PILC).
Other
2018-02-22
EGAS00001002872
Whole genome analysis of mutation hotspots in gastric cancer
Other
2018-02-23
EGAS00001002873
Clonal_haematopoiesis_in_patients_with_AAA
Cancer Genomics
2018-02-23
EGAS00001002874
Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Other
2018-02-23
EGAS00001002875
This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Other
2018-02-24
EGAS00001002876
PanProstate Cancer Group UK data
Other
2018-02-27
EGAS00001002877
Transcriptional and DNA binding profiling of CEBPE in REH acute lymphoblastic leukaemia cells using shRNA RNA-Seq and ChIP-Seq
Other
2018-02-27
EGAS00001002879
RNA-seq of Liver Cancer
Other
2018-02-28
EGAS00001002882
scRNA-seq data of human nuclei collected from the temporal cortex of 17 individuals.
Other
2018-03-01
EGAS00001002884
Genomic analysis of Japanese gastric cancer (345 gastric cancers of NCC)
Other
2018-03-02
EGAS00001002885
Profiling_heterogeneity_in_Human_derived_IPSC_neurons
Transcriptome Analysis
2018-03-02
EGAS00001002886
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Other
2018-03-02
EGAS00001002888
Whole Genome Sequencing of HCC
Other
2018-03-02
EGAS00001002889
Integrated genetic and epigenetic analysis of myxofibrosarcoma
Other
2018-03-02
EGAS00001002891
Exome sequencing of 142 gastric cancer and matched normal from Japanese cohorts (UT)
Other
2018-03-02
EGAS00001002892
Exome sequencing of 102 gastric cancer and matched normal from Japanese cohorts (YCU)
Other
2018-03-02
EGAS00001002893
Exome sequencing demonstrates a dual origin of relapses in retinoic-acid resistant acute promyelocytic leukemia.
Other
2018-03-05
EGAS00001002894
The light chain IgLV3-21 defines a new poor prognostic subgroup in Chronic Lymphocytic Leukemia: results from a multicenter study
Other
2018-03-06
EGAS00001002895
Using human induced pluripotent stem cells (iPSC) and iPSC-derived neurons to explore cellular phenotypes associated with schizophrenia.
Other
2018-03-06
EGAS00001002896
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD
Whole Genome Sequencing
2018-03-07
EGAS00001002897
2015_AML_ETO
Other
2018-03-08
EGAS00001002898
2015_AML_ETO_WGS_additional
Other
2018-03-08
EGAS00001002899
Whole genome characterisation of lung cancer organoids and tissue
Other
2018-03-08
EGAS00001002901
Hypothalamic transcriptome in Prader-Willi syndrome
Other
2018-03-08
EGAS00001002903
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Other
2018-03-09
EGAS00001002907
HG_Retroduplications_in_Neurodevelopmental_Disorders
Whole Genome Sequencing
2018-03-13
EGAS00001002908
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Other
2018-03-13
EGAS00001002910
Molecular analysis of giant cell lesions
Other
2018-03-13
EGAS00001002911
Exploiting immune cell receptor information to quantify index switching in single cell transcriptome sequencing experiment
Other
2018-03-14
EGAS00001002915
Japan PBC-GWAS Haplotype Study
Other
2018-03-14
EGAS00001002917
Human islet 3D chromatin maps provide insights into type 2 diabetes
Other
2018-03-19
EGAS00001002919
Genomic Heterogeneity and the Small Renal Mass
Other
2018-03-20
EGAS00001002920
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Other
2018-03-20
EGAS00001002921
Genome Asia 100K Project
Other
2018-03-20
EGAS00001002922
Leeds Melanoma Cohort (LMC) gene expression study
Other
2018-03-21
EGAS00001002923
Molecular evolution and clinical trajectories of prostate cancer identifies novel markers for risk stratification
Other
2018-03-22
EGAS00001002926
502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Other
2018-03-23
EGAS00001002927
RNA-seq analysis of human skin
Other
2018-03-23
EGAS00001002928
Clinical activity and molecular correlates of response to atezolizumab alone or in combination with bevacizumab versus sunitinib in renal cell carcinoma
Other
2018-03-23
EGAS00001002929
Human_Developmental_Cell_Atlas_HDCA___WGS
Cancer Genomics
2018-03-26
EGAS00001002931
Benchmarking_CRISPR_Whole_genome_Drop_out_Screen___B_S
Cancer Genomics
2018-03-26
EGAS00001002932
RNAseq of 76 samples from Uveal Melanoma tumors
Other
2018-03-26
EGAS00001002933
Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Other
2018-03-27
EGAS00001002935
Infant_Spindle_Tumour_Study
Cancer Genomics
2018-03-27
EGAS00001002936
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Other
2018-03-27
EGAS00001002937
GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project.
Other
2018-03-27
EGAS00001002938
Gastric_Mutational_Signatures__GMS_
Cancer Genomics
2018-03-28
EGAS00001002939
Gastric_Mutational_Signatures__GMS_
Cancer Genomics
2018-03-28
EGAS00001002940
Germline DNMT3A mutation in mother-son pair with AML
Other
2018-03-30
EGAS00001002941
The genomic landscape of lung adenocarcinoma in East Asians
Other
2018-04-03
EGAS00001002945
RNA Sequencing of Colorectal Liver Metastases
Other
2018-04-04
EGAS00001002947
The spatio-temporal evolution of lymph node spread in early breast cancer
Other
2018-04-05
EGAS00001002948
Lymphoctye_colony_WGS
Cancer Genomics
2018-04-05
EGAS00001002951
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Other
2018-04-05
EGAS00001002952
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Other
2018-04-06
EGAS00001002953
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Other
2018-04-06
EGAS00001002954
Whole-genome sequencing reveals genomic signatures associated with the inflammatory microenvironments in Chinese NSCLC patients
Other
2018-04-09
EGAS00001002955
To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Other
2018-04-10
EGAS00001002957
Multiple esclerosis and mixed microbial infections
Other
2018-04-11
EGAS00001002962
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Other
2018-04-17
EGAS00001002963
Inference_of_B_cell_clonality_and_function_from_single_cell_RNA_seq_data
Transcriptome Analysis
2018-04-18
EGAS00001002964
Pre_clinical_evolution_of_haematological_malignancies
Cancer Genomics
2018-04-18
EGAS00001002965
SNP array data for 140 individuals from 5 populations in Pakistan
Other
2018-04-18
EGAS00001002966
Contribution of allelic imbalance to colorectal cancer
Other
2018-04-19
EGAS00001002967
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Other
2018-04-20
EGAS00001002968
Genomic landscape of IG-MYC positive Burkitt lymphoma with precursor B-cell immunophenotype.
Other
2018-04-20
EGAS00001002969
HELIUS cohort
Other
2018-04-20
EGAS00001002972
Single cell exome sequencing of lung adenocarcinoma
Other
2018-04-24
EGAS00001002975
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Other
2018-04-25
EGAS00001002976
H3Africa Chip Design - Aim of designing a cost-effective GWAS chip with content appropriate for use in genomics studies of individuals from the African continent.
Other
2018-04-26
EGAS00001002977
Targeted sequencing about core genes involved in telomere biology in colorectal cancer patients
Other
2018-04-27
EGAS00001002979
Targeted sequencing of head and neck squamous cell carcinomas
Other
2018-04-27
EGAS00001002980
RNAseq of Follicular Lymphoma
Other
2018-04-28
EGAS00001002981
RNA-seq analysis of human primary keratinocytes and skin
Other
2018-04-28
EGAS00001002983
Identification of the mutational consequences of precancerous liver disease (including alcohol abuse) on the genomes of human adult stem cells.
Other
2018-05-02
EGAS00001002987
The whole blood of female volunteers and sperm from the male volunteer were used to extract genomic DNA to do whole genome sequencing. Distinguished SNPs between parental genomes were retained to analyze parental allele-specific DNA methylation and chromatin accessibility in scCOOL-seq data.
Other
2018-05-03
EGAS00001002988
Role_of_HPV_and_Interferon_in_APOBEC_mutational_signature
Cancer Genomics
2018-05-03
EGAS00001002991
Interethnic comparability in blood pressure GWAS
Other
2018-05-07
EGAS00001002993
A benchmarking resource for NGS testing of cancer predisposition genes
Other
2018-05-08
EGAS00001002996
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Other
2018-05-10
EGAS00001002998
Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Other
2018-05-14
EGAS00001002999
Pheno-Seq, linking 3D phenotypes of clonal tumor spheroids to gene expression
Other
2018-05-14
EGAS00001003001
Spatial Transcriptomics on prostate cancer heterogeneity
Other
2018-05-15
EGAS00001003002
Next Generation Children project - WGS study of patients in NICU and PICU and their families
Other
2018-05-15
EGAS00001003003
Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq.
Other
2018-05-15
EGAS00001003004
Genentech study of gallbladder cancer
Other
2018-05-16
EGAS00001003006
Genomic profiling of paediatric glioma cell lines
Other
2018-05-17
EGAS00001003007
Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer
Other
2018-05-17
EGAS00001003008
Age-related remodeling of apparently normal esophageal epithelia by common cancer drivers
Other
2018-05-18
EGAS00001003010
CTCF/cohesin-binding sites are frequently mutated in cancer
Other
2018-05-18
EGAS00001003012
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___WGS
Other
2018-05-18
EGAS00001003014
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___BD___WGS
Other
2018-05-18
EGAS00001003016
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Other
2018-05-21
EGAS00001003017
Celiac disease-specific intestinal T cells analyzed with HLA-class II tetramers, RNA-seq and mass cytometry have a narrow, autoimmune-associated phenotype
Other
2018-05-22
EGAS00001003018
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Other
2018-05-22
EGAS00001003021
Somatic_mutation_and_clonal_evolution_in_the_human_testes
Cancer Genomics
2018-05-23
EGAS00001003023
Somatic_mutation_and_clonal_evolution_in_the_human_testes___WES
Cancer Genomics
2018-05-23
EGAS00001003025
WGS/RNA-seq pair of an inflammatory hepatocellular adenoma (IHCA)
Other
2018-05-24
EGAS00001003026
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Other
2018-05-25
EGAS00001003027
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Other
2018-05-25
EGAS00001003028
The evolutionary history of human colitis-associated colorectal cancer
Other
2018-05-25
EGAS00001003029
Identification of recurrent mutations in Cushing’s disease
Other
2018-05-28
EGAS00001003031
Patient-derived neuroblastoma model system OHC-NB1
Other
2018-05-30
EGAS00001003032
Capture Hi-C on Hodgkin lymphoma cell line L-428
Other
2018-05-31
EGAS00001003033
ChIP-seq data of Hodgkin lymphoma cell line L-428
Other
2018-05-31
EGAS00001003035
AUBTRG - Whole Exome Sequencing of Diffuse Glioma Samples
Cancer Genomics
2018-06-02
EGAS00001003038
Recurrent loss of heterozygosity correlates with clinical outcome in pancreatic neuroendocrine cancer
Other
2018-06-05
EGAS00001003039
Saliva microbiota in Finnish children
Other
2018-06-06
EGAS00001003040
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
Other
2018-06-06
EGAS00001003043
Evolutionary dynamics of residual disease in human glioblastoma
Other
2018-06-06
EGAS00001003044
16S rRNA gene amplification and maternal factors
Other
2018-06-06
EGAS00001003047
SPATC1L variants associated with age-related and hereditary hearing loss
Other
2018-06-06
EGAS00001003048
Whole exome DNA sequence profiling of spatial biopsies of high grade serous epithelial ovarian cancer
Other
2018-06-07
EGAS00001003049
Microdissection_sequencing_of_normal_human_prostate
Cancer Genomics
2018-06-07
EGAS00001003053
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Other
2018-06-09
EGAS00001003054
Indonesian Genome Diversity Project
Other
2018-06-10
EGAS00001003060
CCND1-negative MCL
Other
2018-06-14
EGAS00001003062
Ewings Sarcoma RNA-Seq
Other
2018-06-14
EGAS00001003063
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Other
2018-06-15
EGAS00001003064
Histone chaperone CHAF1A promotes proliferation and tumorigenicity in gastric cancer and impacts prognosis via context-depedent regulation of gene expression
Other
2018-06-15
EGAS00001003065
Control human putamen and Substantia Nigra
Other
2018-06-18
EGAS00001003066
The evolutionary landscape of colorectal tumorigenesis
Other
2018-06-19
EGAS00001003068
Somatic mutations reveal lineage relationships and age-related mutagenesis in human hematopoiesis
Other
2018-06-19
EGAS00001003070
RNA-seq of Glioblastoma stem cells
Other
2018-06-21
EGAS00001003071
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high risk disease
Other
2018-06-22
EGAS00001003072
SLC9A3R1 variant associated with age-related hearing loss
Other
2018-06-22
EGAS00001003073
Ovarian cancer organoid biobank
Other
2018-06-22
EGAS00001003075
Parallel Detections of Somatic Gene Mutations in Surgically Resected Tumor tissues and Matched Plasma Specimens in Early-Stages of Primary Breast Cancer
Other
2018-06-26
EGAS00001003079
RNA sequencing of high hyperdiploid and ETV6/RUNX1-positive pediatric acute lymphoblastic leukemia
Other
2018-06-27
EGAS00001003081
Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes.
Other
2018-06-27
EGAS00001003085
Exome sequencing in bipolar disorder families
Other
2018-06-28
EGAS00001003089
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___TPS___WGS
Other
2018-06-29
EGAS00001003091
HSC_population_dynamics_CBD_samples
Cancer Genomics
2018-07-03
EGAS00001003092
Aneurysmal Subarachnoid Hemorrhage patients with or without vasospasm
Other
2018-07-03
EGAS00001003093
Genomic and transcriptomic profiling of combined hepatocellular and intrahepatic cholangiocarcinoma reveals distinct molecular subtypes
Other
2018-07-03
EGAS00001003094
Bisulphite_MPN_colonies
Cancer Genomics
2018-07-04
EGAS00001003095
Somatic mutations in endometriosis and normal uterine endometrium
Other
2018-07-04
EGAS00001003096
Whole transcriptome RNA sequencing as comprehensive diagnostic tool for acute myeloid leukemia.
Other
2018-07-05
EGAS00001003099
Feasibility Study to Identify the Optimal Adjuvant Combination Scheme of Ipilimumab and Nivolumab (OpACIN) in resectable stage III melanoma patients
Other
2018-07-05
EGAS00001003101
Somatic point mutation data from microsatellite unstable colorectal cancers
Other
2018-07-06
EGAS00001003103
Study of the rare and low frequency variants in the Saguenay-Lac-Saint-Jean population
Other
2018-07-06
EGAS00001003104
Primary plasma cell leukemia (pPCL) samples were sequenced using the Nimblegen MedExome hybridization capture to detect translocations, copy number changes, and mutations in 20 pPCL samples and patient matched controls.
Other
2018-07-06
EGAS00001003105
Microbial signatures and innate immune gene expression in lamina propria phagocytes of inflammatory bowel diseases patients
Other
2018-07-07
EGAS00001003108
Whole genome amplification and whole genome sequencing of human single cells
Other
2018-07-10
EGAS00001003110
Circulating cell-free DNA analysis in Small Cell Lung Cancer
Other
2018-07-10
EGAS00001003112
Whole_genome_sequencing_of_in_vitro_colonies
Other
2018-07-11
EGAS00001003113
Frequent mutation of the FOXA1 untranslated region in prostate cancer
Other
2018-07-12
EGAS00001003114
Reconstruction of human terminal erythroid differentiation cell at single cell level
Transcriptome Analysis
2018-07-13
EGAS00001003115
Organoid Models of Human Liver Cancers Derived from Tumor Needle Biopsies
Cancer Genomics
2018-07-15
EGAS00001003116
DNA-seq from plasma of 14 liver transplantation patients
Other
2018-07-16
EGAS00001003117
BS-seq in plasma of CRC patients
Other
2018-07-16
EGAS00001003118
Histone acetylome-wide association study on tuberculosis infection
Other
2018-07-17
EGAS00001003119
Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Other
2018-07-17
EGAS00001003121
Resolving the Full Spectrum of Human Genome Variation using Linked-Reads
Other
2018-07-18
EGAS00001003122
Oesophageal_Adenocarcinoma_Organoid_Hi_C
Cancer Genomics
2018-07-19
EGAS00001003123
Heritable pulmonary arterial hypertension in a large Iberian family
Other
2018-07-19
EGAS00001003127
Understanding human fetal pancreas development using subpopulation sorting and RNA sequencing
Other
2018-07-20
EGAS00001003128
Circular RNA characterization in functionally distinct brain regions
Other
2018-07-23
EGAS00001003130
Exome sequencing of advanced hepatocellular carcinoma
Other
2018-07-25
EGAS00001003131
WES+WGS OSCCs Boot et al. 2018
Other
2018-07-27
EGAS00001003136
Open_Targets_020_Epigenomes_of_Cell_Lines
Epigenetics
2018-07-31
EGAS00001003137
Open_Targets_020_Epigenomes_of_Cell_Lines
Epigenetics
2018-07-31
EGAS00001003138
Open_Targets_020_Epigenomes_of_Cell_Lines
Transcriptome Analysis
2018-07-31
EGAS00001003139
Open_Targets_020_Epigenomes_of_Cell_Lines
Epigenetics
2018-07-31
EGAS00001003140
Automated image-based profiling of complex drug induced phenotypes in patient-derived organoids
Other
2018-07-31
EGAS00001003142
Whole exome sequencing of small cell neuroendocrine cancer of the cervix
Other
2018-07-31
EGAS00001003144
Single cell sequencing of endoscopic biopsies from Barrett's oesophagus and proximal tissue from the normal GI tract
Other
2018-08-01
EGAS00001003145
A comprehensive human gastric cancer organoid biobank captures tumor subtype heterogeneity and enables therapeutic screening
Other
2018-08-02
EGAS00001003147
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Other
2018-08-02
EGAS00001003148
Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions
Whole Genome Sequencing
2018-08-03
EGAS00001003151
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Cancer Genomics
2018-08-08
EGAS00001003154
Sequencing_of_patient_samples_who_received_immune_checkpoint_inhibition___WES___NKI
Cancer Genomics
2018-08-09
EGAS00001003157
Partially methylated domains across multiple cell types
Other
2018-08-10
EGAS00001003158
DNA Methylation-based diagnostic biomarkers for ESCC in Han Chinese population
Other
2018-08-10
EGAS00001003159
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Other
2018-08-14
EGAS00001003160
Tumor-associated preferred end coordinates and somatic variants as signatures of circulating tumor DNA
Other
2018-08-15
EGAS00001003162
Single_cell_resolution_of_human_CNV_body_map
Cancer Genomics
2018-08-15
EGAS00001003163
ChIP-seq data of H3K4me3, H3K27ac and H3K27me3 on multiple human embryonic tissues.
Other
2018-08-16
EGAS00001003164
Whole genome sequencing of multiple myeloma identifies novel structural and non-coding mutations.
Other
2018-08-16
EGAS00001003165
iNeuron_ChIPseq
Other
2018-08-16
EGAS00001003167
Repeated_clinical_malaria_episodes_are_associated_with_modification_of_the_immune_system_in_children_
Transcriptome Analysis
2018-08-20
EGAS00001003168
Primary breast tumor heterogeneity through therapy
Cancer Genomics
2018-08-20
EGAS00001003170
Childhood cerebellar tumors mirror conserved fetal transcriptional programs
Other
2018-08-21
EGAS00001003171
High Altitude Pulmonary Hypertension
Other
2018-08-22
EGAS00001003172
“Castration-persistence” is a distinct state of tolerance to androgen receptor targeting therapies in prostate cancer
Other
2018-08-22
EGAS00001003173
Primary breast cancers and paired brain metastases sequencing study
Other
2018-08-22
EGAS00001003174
Dnase1l3 knockout causes aberrations in plasma DNA fragmentation
Other
2018-08-22
EGAS00001003175
Targeted_sequencing_of_in_vitro_colonies___bulks
Cancer Genomics
2018-08-23
EGAS00001003176
Study the differences at the trascriptome level between iNKT and T cells
Other
2018-08-24
EGAS00001003177
A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy
Other
2018-08-27
EGAS00001003178
Neoadjuvant immune checkpoint blockade in high-risk resectable melanoma
Other
2018-08-27
EGAS00001003179
Molecular origins of mpMRI visibility
Other
2018-08-28
EGAS00001003180
Profiling of Peritoneal Metastases from Gastric Adenocarcinoma Identified Molecular Subtypes
Other
2018-08-29
EGAS00001003181
Population_dynamics_in_abnormal_haematopoiesis
Other
2018-08-29
EGAS00001003183
ImmunoAgeing_Longitudinal
Other
2018-08-30
EGAS00001003184
Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples
Other
2018-08-30
EGAS00001003185
BCR_repertoire_sequencing
Resequencing
2018-08-31
EGAS00001003186
The molecular landscape of glioma in patients with Neurofibromatosis 1.
Other
2018-08-31
EGAS00001003190
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing
Other
2018-09-05
EGAS00001003191
Oesophageal_Adenocarcinoma_Organoid_10x
Cancer Genomics
2018-09-05
EGAS00001003193
Improving CLL Vγ9Vδ2-T cell fitness for cellular therapy by ex vivo activation and ibrutinib
Other
2018-09-07
EGAS00001003195
Low frequency and rare coding variation contributes to multiple sclerosis risk
Other
2018-09-08
EGAS00001003197
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas_LCM_
Cancer Genomics
2018-09-10
EGAS00001003199
Genome-wide association study of cervical cancer in East Asian populations
Other
2018-09-11
EGAS00001003200
Exploiting evolutionary steering in cancer therapy
Other
2018-09-11
EGAS00001003201
Whole genome and RNAseq analysis of pediatric osteosarcoma
Other
2018-09-11
EGAS00001003203
Hyperhaploid Multiple Myeloma
Other
2018-09-11
EGAS00001003206
Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Other
2018-09-12
EGAS00001003207
Whole exome sequencing of 76 individuals with familial atrial fibrillation
Other
2018-09-12
EGAS00001003208
early onset lone atrial fibrillation case-control study
Other
2018-09-12
EGAS00001003209
PAX5 biallelic genomic alterations define a novel subgroup of B cell precursor acute lymphoblastic leukemia
Other
2018-09-13
EGAS00001003212
Structure and evolution of double minutes in diagnosis and relapse brain tumors
Other
2018-09-14
EGAS00001003213
ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer
Other
2018-09-14
EGAS00001003214
FBSeq: RNA sequencing of human fetal brain.
Other
2018-09-15
EGAS00001003215
Single_cell_analysis_of_cytokine_induced_T_cell_states
Transcriptome Analysis
2018-09-18
EGAS00001003216
Multiple Sclerosis Replication Chip data (MS Chip)
Other
2018-09-18
EGAS00001003217
Fecal Microbiota Transplantation for refractory immune checkpoint inhibitor-associated colitis
Other
2018-09-18
EGAS00001003219
Multiple Sclerosis ImmunoChip data
Other
2018-09-18
EGAS00001003220
Alternative splicing in Shh-MB
Other
2018-09-18
EGAS00001003221
Temporal stability of circulating microRNAs in human serum
Other
2018-09-19
EGAS00001003223
Multiple Myeloma Total Therapy trial patient sequencing
Other
2018-09-19
EGAS00001003225
Genomic profiling of esthesioneuroblastoma
Other
2018-09-20
EGAS00001003227
Whole Exome Sequencing in Multiple Myeloma
Other
2018-09-24
EGAS00001003228
Genomic landscape of oral cancers (Illumina WGS)
Other
2018-09-24
EGAS00001003231
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Other
2018-09-25
EGAS00001003232
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Other
2018-09-25
EGAS00001003233
Molecular Classification of Lymph Node Metastases Subtypes Predict for Survival in Head and Neck Cancer
Transcriptome Analysis
2018-09-26
EGAS00001003234
An exome sequencing approach to defining the genetic risk factors for Achilles tendinopathy
Other
2018-09-26
EGAS00001003235
Oncogenic fate conversion by PRDM16s causes acute myeloid leukemia
Other
2018-09-26
EGAS00001003236
Discovery of new fusion transcripts in a cohort of pediatric solid cancers at relapse
Other
2018-09-26
EGAS00001003237
Genomic landscape of oral cancers (Illumina RNA-Seq)
Other
2018-09-26
EGAS00001003238
Fibroblast heterogeneity drives metastatic spread in breast cancer through distinct mechanisms
Other
2018-09-28
EGAS00001003239
The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels
Other
2018-10-01
EGAS00001003242
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Other
2018-10-02
EGAS00001003244
A mechanistic classification of clinical phenotypes in neuroblastoma
Other
2018-10-02
EGAS00001003245
Single-cell TCR sequencing of gluten-specific T cells
Other
2018-10-02
EGAS00001003247
Characterizing the immune and genome landscapes for osteosarcoma
Other
2018-10-02
EGAS00001003248
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Other
2018-10-04
EGAS00001003249
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD_Full_STDY
Whole Genome Sequencing
2018-10-04
EGAS00001003250
1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Other
2018-10-04
EGAS00001003251
Infiltrative and drug-resistant slow-cycling cells support metabolic heterogeneity in glioblastoma
Other
2018-10-05
EGAS00001003252
A Study to Evaluate Denosumab in Young Patients With Primary Breast Cancer (D-Beyond)
Other
2018-10-08
EGAS00001003254
46 CLL Whole Genome Sequencing Study
Other
2018-10-09
EGAS00001003255
Detection of cell-free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients
Other
2018-10-09
EGAS00001003256
Molecular Characterization of ETMRs
Other
2018-10-09
EGAS00001003257
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Other
2018-10-09
EGAS00001003258
Enhanced detection of circulating tumor DNA by fragment size analysis
Other
2018-10-09
EGAS00001003263
Analysis of translatome, truncating mutations, lncRNA, circRNA and microproteins of 80 human DCM cases and controls
Other
2018-10-15
EGAS00001003264
X10_sequencing_of_Oesophageal_Adenocarcinoma_Organoids
Cancer Genomics
2018-10-16
EGAS00001003266
Mullighan - PAX5-driven Subtypes
Other
2018-10-16
EGAS00001003274
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Other
2018-10-18
EGAS00001003275
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Other
2018-10-18
EGAS00001003276
Butyrate producers as potential next-generation probiotics: safety assessment of the administration of Butyricicoccus pullicaecorum to healthy volunteers
Other
2018-10-18
EGAS00001003278
A GWAS meta-analysis on severe acne on a European population of 26,722 individuals
Other
2018-10-22
EGAS00001003280
INSPIRE - Investigator-initiated Phase 2 Study of Pembrolizumab Immunological Response in Metastatic Solid Tumors
Cancer Genomics
2018-10-25
EGAS00001003281
Mutations of whole genome sequencing in single cells in normal esophageal epithelium
Other
2018-10-29
EGAS00001003282
Paired whole exome sequence of subcutaneous panniculitis-like T-cell lymphoma.
Other
2018-10-29
EGAS00001003284
Molecular profiling of longitudinally observed small colorectal polyps: a cohort study
Other
2018-10-30
EGAS00001003285
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_Batch05
Other
2018-10-30
EGAS00001003286
Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat
Other
2018-10-31
EGAS00001003288
Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness
Other
2018-11-01
EGAS00001003290
Genomic characterization of metastatic breast cancers
Other
2018-11-05
EGAS00001003291
RNA sequencing of undifferentiated sarcomas
Other
2018-11-05
EGAS00001003292
Whole Tumor spatial heterogeneity in metastatic melanoma
Other
2018-11-05
EGAS00001003293
Pseudotime_ordering_of_cell_cycle_state
Cancer Genomics
2018-11-06
EGAS00001003295
SEARCH FOR BACTERIA IN NEURAL TISSUE FROM AMYOTROPHIC LATERAL SCLEROSIS
Other
2018-11-07
EGAS00001003296
1054 Flemish Gut Flora Project (FGFP) samples (16S sequencing, dual index)
Other
2018-11-07
EGAS00001003297
Placental_genomics
Cancer Genomics
2018-11-08
EGAS00001003298
FGFP and TR-MDD shotgun sequencing samples (N=157)
Other
2018-11-08
EGAS00001003300
Acquiring and sequencing of all 24 single human chromosomes
Other
2018-11-09
EGAS00001003302
Tetralogy of fallot whole-exome sequencing
Other
2018-11-10
EGAS00001003303
Genetic alterations in metastatic uveal melanoma
Cancer Genomics
2018-11-11
EGAS00001003305
Whole genome sequencing of tumour and matched normal from patients with family history of breast cancer
Other
2018-11-13
EGAS00001003306
Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer
Other
2018-11-13
EGAS00001003307
Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer RNA-Seq
Other
2018-11-13
EGAS00001003309
The analysis of mtDNA variability of the modern Polish population
Other
2018-11-13
EGAS00001003310
Adeno-associated virus in the liver: natural history and consequences in tumor development
Other
2018-11-13
EGAS00001003311
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Other
2018-11-14
EGAS00001003313
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Other
2018-11-14
EGAS00001003315
MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Targeted_
Cancer Genomics
2018-11-14
EGAS00001003316
MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Exome_
Cancer Genomics
2018-11-14
EGAS00001003317
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__WG_
Cancer Genomics
2018-11-14
EGAS00001003318
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Targeted_
Cancer Genomics
2018-11-14
EGAS00001003319
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Exome_
Cancer Genomics
2018-11-14
EGAS00001003320
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__WG_
Cancer Genomics
2018-11-14
EGAS00001003321
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_
Cancer Genomics
2018-11-14
EGAS00001003322
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD38233__WG_
Cancer Genomics
2018-11-14
EGAS00001003324
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD38234__WG_
Cancer Genomics
2018-11-14
EGAS00001003325
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD38234__Targeted_
Cancer Genomics
2018-11-14
EGAS00001003329
H014: HES5 mediates NOTCH signaling by interaction with AKT to drive liver carcinogenesis
Other
2018-11-15
EGAS00001003331
SNP array datas of 'Matched' cancer/PNE
Other
2018-11-15
EGAS00001003332
RNAseq data from human colon organoid infected by KP
Other
2018-11-16
EGAS00001003333
RNA-seq of Ewing sarcoma tumors (ICGC)
Other
2018-11-19
EGAS00001003335
Genome-wide characterization of Arabian Peninsula populations
Other
2018-11-21
EGAS00001003337
Naive B-cell receptor heavy chain repertoire of celiac patients and healthy controls
Other
2018-11-21
EGAS00001003341
MGA-NUTM1 fusion in high grade spindle cell sarcoma
Other
2018-11-22
EGAS00001003342
WGS and WES of pediatric osteosarcoma
Other
2018-11-22
EGAS00001003343
Exome sequencing of a novel cervical cancer cell line
Other
2018-11-23
EGAS00001003344
CAF-S3 subset in human breast and ovarian cancers
Other
2018-11-26
EGAS00001003345
Small intestinal plasma cells transcriptome profiles
Other
2018-11-26
EGAS00001003346
HG Transcriptome sequencing in the INTERVAL cohort
Other
2018-11-26
EGAS00001003349
WTCCC2 Pre-eclampsia Study
Other
2018-11-28
EGAS00001003350
ALPI deficiency causes refractory Inflammation Bowel Disease
Other
2018-11-28
EGAS00001003351
Circulating tumour DNA abundance and potential utility in de novo metastatic prostate cancer
Other
2018-11-29
EGAS00001003352
Evaluation of commercial Guardant360 ctDNA test in metastatic prostate cancer
Other
2018-11-29
EGAS00001003353
Non-coding RNAs in breast cancer
Other
2018-11-29
EGAS00001003354
Neoadjuvant chemotherapy alters the genomic landscape and immune microenvironment of breast cancers
Other
2018-11-30
EGAS00001003355
Gene expression in CSF and blood of patients with pneumococcal meningitis
RNASeq
2018-11-30
EGAS00001003357
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis -Part II
Other
2018-12-02
EGAS00001003358
Small intestinal neuroendocrine tumors
Other
2018-12-02
EGAS00001003359
Ancient nuclear genomes enable repatriation of Indigenous human remains
Other
2018-12-02
EGAS00001003360
organoid data of colorectal cancers
Whole Genome Sequencing
2018-12-03
EGAS00001003361
Forty-Five patient-derived xenografts capture the clinical and biological heterogeneity of Wilms tumor
Other
2018-12-03
EGAS00001003362
Uveal melanoma patient with germline MBD4 nonsense mutation
Other
2018-12-04
EGAS00001003363
Single-cell RNA-seq of immune cells sorted from human melanoma tumors
Other
2018-12-04
EGAS00001003365
Finding structural variation from the patient-derived xenografts of pediatric T-cell leukemia at the single-cell level
Other
2018-12-05
EGAS00001003366
Microsatellite unstable colorectal cancers
Other
2018-12-06
EGAS00001003367
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Other
2018-12-06
EGAS00001003368
Single-cell atlas of the developing brain to investigate the cellular origins of pediatric brain tumors
RNASeq
2018-12-06
EGAS00001003369
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Other
2018-12-07
EGAS00001003370
Mutational Patterns in Metastatic Cutaneous Squamous Cell Carcinoma
Other
2018-12-10
EGAS00001003372
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Other
2018-12-10
EGAS00001003380
PTPN22 SNPs and outcome after lung transplantation
Other
2018-12-12
EGAS00001003382
Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing
Other
2018-12-12
EGAS00001003383
ProjectMinE :llumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Other
2018-12-12
EGAS00001003384
Lymphocyte_LCM_WGS
Cancer Genomics
2018-12-12
EGAS00001003385
Whole genome sequencing of Ewings Sarcoma
Other
2018-12-12
EGAS00001003386
Nuclear_single_seq_pilot
Cancer Genomics
2018-12-12
EGAS00001003387
Single cell RNA sequencing and Whole Genome Sequencing on different cells from the same sample for a triple negative patient derived xenograft and ovarian cancer cell lines.
Other
2018-12-12
EGAS00001003388
Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer
Other
2018-12-13
EGAS00001003396
Hepatocellular carcinoma xenografts established from needle biopsies preserve the characteristics of the originating tumors
Transcriptome Analysis
2018-12-17
EGAS00001003397
HSC_population_dynamics___CB001_samples
Cancer Genomics
2018-12-17
EGAS00001003399
Familial Myeloid Leukemia
Other
2018-12-17
EGAS00001003400
Whole-exome sequencing of NTHL1 deficient tumors
Exome Sequencing
2018-12-18
EGAS00001003405
KIT-dependent and -independent genomic heterogeneity of resistance in gastrointestinal stromal tumors - TORC1/2 inhibition as salvage strategy
Other
2018-12-19
EGAS00001003406
Sequencing Study in COPD cases and controls
Other
2018-12-19
EGAS00001003407
Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study
Other
2018-12-21
EGAS00001003408
Methylation analysis of plasma DNA informs etiologies of Epstein-Barr virus-associated diseases
Other
2018-12-26
EGAS00001003409
Plasma DNA motif analysis
Other
2018-12-26
EGAS00001003411
RNA sequencing of multiple myeloma identifies genes dysregulated by structural variants.
Other
2018-12-27
EGAS00001003412
Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing
Other
2018-12-31
EGAS00001003414
Mutation tracking in single cell RNA-Seq reveals consequences of subclonal evolution in acute myeloid leukemia
Other
2019-01-02
EGAS00001003415
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
Other
2019-01-02
EGAS00001003418
Landscape of somatic mutations and DNA copy number alterations and transcriptomic profiling identifies metabolic reprogramming as a hallmark of ibrutinib resistance
Other
2019-01-08
EGAS00001003419
16S-based fecal microbiota composition of the Milieu Intérieur Cohort
Other
2019-01-08
EGAS00001003421
STREP GENE: Genetics and Severe Streptococcal Infections
Other
2019-01-09
EGAS00001003423
Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Other
2019-01-11
EGAS00001003424
Genome Wide Association Study:GR@ACE Stage I
Other
2019-01-14
EGAS00001003425
the Yemeni-Somali 5 million SNP array dataset
Other
2019-01-14
EGAS00001003426
Panel-based next-generation sequencing study of human liver samples.
Other
2019-01-14
EGAS00001003427
Combined MEK and BCL-2/XL inhibition is effective in high-grade serous ovarian cancer patient-derived xenograft models and BIM levels are predictive of responsiveness
Other
2019-01-15
EGAS00001003428
Genomic_profiling_of_B_other_Adult_ALL_RNA
Other
2019-01-16
EGAS00001003430
Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Other
2019-01-16
EGAS00001003432
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Other
2019-01-17
EGAS00001003433
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_Novaseq
Whole Genome Sequencing
2019-01-18
EGAS00001003434
Extreme intratumor heterogeneity and driver evolution in mismatch repair deficient gastro-esophageal cancer
Cancer Genomics
2019-01-21
EGAS00001003436
SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons
Other
2019-01-21
EGAS00001003437
Paediatric Tumour Profiling
Other
2019-01-21
EGAS00001003438
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Other
2019-01-22
EGAS00001003439
Multi-region exome sequencing of lung adenocarcinoma precursors -1
Other
2019-01-22
EGAS00001003442
Functional and genomic heterogeneity of long-term self-renewing compartment as the origin of treatment resistance in pancreatic tumors
Other
2019-01-23
EGAS00001003443
Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution
Other
2019-01-24
EGAS00001003444
Analysis of error profiles in deep next-generation sequencing data
Other
2019-01-24
EGAS00001003445
Orphan_Tumour_Study_NB
Transcriptome Analysis
2019-01-25
EGAS00001003446
Liver_Tumours_WGS
Whole Genome Sequencing
2019-01-25
EGAS00001003447
Clonal architectures predict clinical outcome in clear cell renal cell carcinoma
Other
2019-01-26
EGAS00001003449
Single-cell RNA sequencing on single CD45+ immune cells isolated from peripheral blood, lymphnode, ascites, tumour and adjacent normal tissues from six hepatocellular carcinoma patients.
Other
2019-01-27
EGAS00001003450
MCO colorectal cancer genomics at UNSW
Other
2019-01-28
EGAS00001003451
RNA-seq of M-CSF differentiated human peripheral monocyte-derived macrophages (MDMs) - Validation macIDR
Other
2019-01-28
EGAS00001003452
Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers
Other
2019-01-28
EGAS00001003453
Molecular profiling of blastic plasmacytoid dendritic cell neoplasm (BPDCN) as compared to acute myeloid leukemia (AML)
Other
2019-01-29
EGAS00001003454
Molecular Phenotype of Constitutional TET2 Haploinsufficiency in Humans
Other
2019-01-31
EGAS00001003455
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Whole Genome Sequencing
2019-01-31
EGAS00001003456
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WES_NOVASEQ
Other
2019-01-31
EGAS00001003457
GermCellTumour
Whole Genome Sequencing
2019-02-01
EGAS00001003458
TRACERx 100: RNAseq data from the first 100 TRACERx tumours
Other
2019-02-01
EGAS00001003460
GWAS and Meta-analysis on Frontal Fibrosing Alopecia in two European Populations
Other
2019-02-05
EGAS00001003462
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Other
2019-02-07
EGAS00001003463
Exome sequencing of stroke cases with good or bad recovery three months after stroke
Other
2019-02-08
EGAS00001003465
Identification_of_immune_mechanisms_associated_with_the_high_rate_of_relapse_in_patient_with_visceral_leishmaniasis_and_HIV_co_infection
Transcriptome Analysis
2019-02-11
EGAS00001003467
Placental multi-omics data-mining in Intra-Uterine Growth Restriction
Other
2019-02-11
EGAS00001003468
Adenoma to Carcinoma transition in Colorectal Cancer
Other
2019-02-12
EGAS00001003469
We evaluate the potential for routine WGS using ONT by sequencing the well-characterised reference sample NA12878 and the genome of an individual with ataxia-pancytopenia syndrome accompanied by severe immune dysregulation.
Other
2019-02-12
EGAS00001003471
Dedifferentiated_Melanoma
Cancer Genomics
2019-02-13
EGAS00001003474
Exome sequencing of synchronous colorectal cancers
Other
2019-02-14
EGAS00001003479
Single_cell_analysis_T_cell_activation
Other
2019-02-15
EGAS00001003481
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Other
2019-02-15
EGAS00001003484
TRACERx 100: RRBS data from a subset of the first 100 TRACERx tumours
Other
2019-02-18
EGAS00001003485
Chromatin 3D interactions mediate genetic effects on gene expression
Other
2019-02-18
EGAS00001003486
Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms
Other
2019-02-18
EGAS00001003487
Combined gene expression and digital pathology identifies molecular mediators of T cell exclusion and immune suppression in ovarian cancer
Other
2019-02-20
EGAS00001003488
Growth Hormone (GH) -secreting Pituitary Adenoma
Other
2019-02-20
EGAS00001003489
Molecular phenotyping of MCA/ID patients to improve diagnosis
Other
2019-02-20
EGAS00001003490
Predicting brain tumor recurrence: development and validation of a DNA-methylation based nomogram in meningioma
Other
2019-02-20
EGAS00001003493
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Other
2019-02-20
EGAS00001003496
Somatic mutations increase hepatic clonal fitness and regeneration in chronic liver disease
Other
2019-02-21
EGAS00001003497
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Other
2019-02-22
EGAS00001003498
DIME study: Safety, dose-response and efficacy of treatment with Anaerobutyricum soehgenii on glucose metabolism in human subjects with metabolic syndrome
Other
2019-02-22
EGAS00001003499
EXCEED Study
Other
2019-02-24
EGAS00001003500
Whole-genome sequencing of Tibetans from China
Other
2019-02-25
EGAS00001003501
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Epigenetics
2019-02-26
EGAS00001003502
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Other
2019-02-26
EGAS00001003503
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__Exome_
Other
2019-02-26
EGAS00001003504
Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data
Other
2019-02-27
EGAS00001003506
Analysis of Multiparametric MR imaging and tumor tissue sampling to identify response and acquired resistance to HIF-2 inhibition in patients with advanced clear cell renal cell carcinoma enrolled in a phase 1, multiple-dose, dose-escalation trial of PT2385, a HIF-2alpha inhibitor
Cancer Genomics
2019-02-27
EGAS00001003507
Fixation effects on variant-calling in a clinical resequencing panel
Other
2019-02-28
EGAS00001003508
300-Obese: clinical cohort of obese individuals, Nijmegen, the Netherlands
Other
2019-03-01
EGAS00001003510
Juvenile Idiopathic Arthritis exome sequencing in a consanguineous family
Other
2019-03-03
EGAS00001003511
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Other
2019-03-04
EGAS00001003512
whole-genome sequencing of gastric cancer
Other
2019-03-04
EGAS00001003513
Comparison of 3 protocols for deriving pancreatic progenitors from hPSC with RNA-seq and ATAC-seq
Other
2019-03-04
EGAS00001003514
The biology of cell-free DNA fragmentation and the roles ofDNASE1, DNASE1L3 and DFFB
Other
2019-03-05
EGAS00001003515
Gene regulation of human stimulated and cultured CD4+ Treg cells
Other
2019-03-05
EGAS00001003516
Gene_regulation_of_human_CD4__Treg_cells_
Other
2019-03-05
EGAS00001003517
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Whole Genome Sequencing
2019-03-07
EGAS00001003519
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Transcriptome Analysis
2019-03-07
EGAS00001003520
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Whole Genome Sequencing
2019-03-08
EGAS00001003521
Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants
Other
2019-03-09
EGAS00001003523
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___WG__Novaseq_
Other
2019-03-11
EGAS00001003524
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Other
2019-03-11
EGAS00001003525
MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__WG__Novaseq_
Whole Genome Sequencing
2019-03-11
EGAS00001003526
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Other
2019-03-11
EGAS00001003527
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Other
2019-03-11
EGAS00001003528
MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_
Other
2019-03-11
EGAS00001003530
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Other
2019-03-12
EGAS00001003531
Melanoma_post_mortem_analysis
Cancer Genomics
2019-03-13
EGAS00001003532
Sequencing of Infant high grade gliomas
Other
2019-03-13
EGAS00001003534
The landscape of LAM disease
Other
2019-03-14
EGAS00001003535
Immune induction strategies to enhance the sensitivity to PD-1 blockade in metastatic triple negative breast cancer: the TONIC-trial
Other
2019-03-14
EGAS00001003536
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Other
2019-03-15
EGAS00001003538
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Cancer Genomics
2019-03-15
EGAS00001003539
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Other
2019-03-15
EGAS00001003540
Genomic and transcriptomic landscape of aggressive thyroid cancer
Other
2019-03-16
EGAS00001003541
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___UGI___WGS
Other
2019-03-18
EGAS00001003542
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Other
2019-03-18
EGAS00001003544
RNA sequencing of NK cells in human lung
Other
2019-03-18
EGAS00001003545
Genomics analysis of mucinous tumours of the ovary and related neoplasms
Other
2019-03-19
EGAS00001003546
Evolution of GBM through therapy
Other
2019-03-20
EGAS00001003547
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Cancer Genomics
2019-03-20
EGAS00001003548
Rare coding variants in lupus risk genes
Other
2019-03-21
EGAS00001003549
Placental_mosaicism
Cancer Genomics
2019-03-21
EGAS00001003550
HSC_population_dynamics___KX003_samples
Whole Genome Sequencing
2019-03-21
EGAS00001003553
To_profile_the_landscape_of_sebaceous_tumours_WES
Cancer Genomics
2019-03-22
EGAS00001003554
Arriba: accurate and efficient detection of gene fusions from RNA-Seq (H021)
Other
2019-03-22
EGAS00001003555
Revealing active mutational processes in tumours using DigiPico/MutLX at unprecedented accuracy
Other
2019-03-24
EGAS00001003556
Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers
Other
2019-03-25
EGAS00001003558
Colorectal cancer organoids expressing BRAF (fusion) genes
Other
2019-03-26
EGAS00001003560
Genetic modification of primary human B cells to model high-grade lymphoma
RNASeq
2019-03-27
EGAS00001003563
Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients
Other
2019-03-29
EGAS00001003564
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Other
2019-03-30
EGAS00001003565
South Asia Rheumatic Heart Disease Genetics Network
Other
2019-04-01
EGAS00001003570
Whole-genome sequencing of normal Singaporean volunteers
Population Genomics
2019-04-03
EGAS00001003571
Understanding_Self__Organising_Capacity_of_Stem_Cells_during_Implantation_and_Early_Post_implantation_Development_in_vitro_and_in_vivo__Implications_for_Human_Development_
Transcriptome Analysis
2019-04-03
EGAS00001003572
Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability
Other
2019-04-03
EGAS00001003573
Multi-Region WES of Metastatic Colorectal Cancer
Cancer Genomics
2019-04-03
EGAS00001003575
RNA-sequencing of adult T-cell leukemia/lymphoma samples
Other
2019-04-04
EGAS00001003576
Cancer-Associated Mutations in Endometriosis without Cancer
Other
2019-04-04
EGAS00001003579
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Other
2019-04-05
EGAS00001003582
Phylogenetic evolution of metastatic melanoma.
Other
2019-04-08
EGAS00001003583
Genetic dysregulation of gene expression and splicing during a ten-year period of human aging in the PIVUS study
Other
2019-04-09
EGAS00001003585
Gut microbiota analysis after 3months probiotic-like bacteria or placebo treatment in subjects with metabolic syndrome
Other
2019-04-09
EGAS00001003586
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Other
2019-04-09
EGAS00001003590
Investigation of human variation in healthy individuals on gene and protein levels
Other
2019-04-10
EGAS00001003592
5- FU treated organoids
Other
2019-04-12
EGAS00001003594
Lymphocyte_Gut_WGS_H38
Whole Genome Sequencing
2019-04-12
EGAS00001003596
Lymphocyte_PanBody_WGS_H38
Whole Genome Sequencing
2019-04-12
EGAS00001003598
Single cell transcriptomic and genomic profiling of carcinogenesis in patients with familial adenomatous polyposis
Other
2019-04-15
EGAS00001003599
Whole exome sequencing of trio with primary immunodeficiency (IL2RB)
Other
2019-04-15
EGAS00001003600
Quantitative microbiome profiling disentangles inflammation- and bile duct obstruction-associated microbiota alterations across IBD/PSC diagnoses
Other
2019-04-16
EGAS00001003601
Dedifferentiated_Melanoma_RNAseq
Cancer Genomics
2019-04-17
EGAS00001003602
GDAP___Genome_Diversity_in_Africa_Project
Whole Genome Sequencing
2019-04-18
EGAS00001003603
Genetic and expression landscape of Waldenstrom macroglobulinemia
Other
2019-04-18
EGAS00001003605
A Phase II Trial of High Dose Interleukin-2 and Multi-site Stereotactic Ablative Radiotherapy for Patients with Metastatic Renal Cell Carcinoma
Other
2019-04-18
EGAS00001003607
GWAS Steroid Sensitive Nephrotic Syndrome
Population Genomics
2019-04-22
EGAS00001003611
Genome-wide cell-free DNA fragmentation in patients with cancer
Other
2019-04-24
EGAS00001003616
Kidney_tumour_DNA_exome
Other
2019-04-26
EGAS00001003617
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Other
2019-04-26
EGAS00001003620
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Other
2019-04-26
EGAS00001003623
Novel PARN mutations in Hoyeraal-HReidarsson syndrome patients.
Other
2019-04-29
EGAS00001003624
WGS of Roma (Romani/Rroma) and European/Romanian individuals from Romania
Other
2019-04-29
EGAS00001003626
Mutations conferring differential treatment response in breast cancer
Other
2019-04-29
EGAS00001003627
Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia
Epigenetics
2019-04-30
EGAS00001003628
Oral mucosa organoids as a potential model for personalized therapies
Other
2019-04-30
EGAS00001003629
UAMS Smoldering Myeloma Myeloma Sequencing
Other
2019-04-30
EGAS00001003631
Breast Cancer - immune clusters - RNA-seq
Other
2019-04-30
EGAS00001003633
CRC GWAS on the Spanish population
Other
2019-05-02
EGAS00001003634
Non-invasive prenatal diagnosis by genome-wide haplotyping of maternal cell-free plasma DNA
Other
2019-05-02
EGAS00001003635
Genome‐wide postnatal changes in immunity following fetal inflammatory response
Other
2019-05-02
EGAS00001003638
Effect of 28-day administration of Urolithin A to sedentary elderly on muscle gene expression
Other
2019-05-03
EGAS00001003639
Genome-wide search to find the genetic elements underlying visual contour perception
Other
2019-05-04
EGAS00001003642
Pangenomic classification of pituitary adenomas
Other
2019-05-07
EGAS00001003643
Presence of bacterial infection in brains of patients with Parkinson's disease (PD)
Other
2019-05-07
EGAS00001003644
Presence of fungal infection in brains of patients with Parkinsons disease (PD)
Other
2019-05-07
EGAS00001003645
GWAS Results from Danjou et al, Nature Genetics 2015
Other
2019-05-07
EGAS00001003646
Latency and interval therapy affect the evolution in metastatic colorectal cancer
Other
2019-05-07
EGAS00001003647
Mapping_genetic_variants_underlying_gene_regulation_in_healthy_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Transcriptome Analysis
2019-05-08
EGAS00001003648
Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania
Other
2019-05-08
EGAS00001003650
WGBS analysis corresponding to representative cases of iBCP-ALL patients
Other
2019-05-10
EGAS00001003651
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Other
2019-05-12
EGAS00001003652
Accelerated clonal evolution in refractory versus relapsed chronic lymphocytic leukemia upon treatment
Other
2019-05-13
EGAS00001003653
Indonesian methylation data
Other
2019-05-15
EGAS00001003654
Indonesian Genome Diversity Project 2
Other
2019-05-16
EGAS00001003656
Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice
Other
2019-05-17
EGAS00001003657
Human pan-genome analysis
Other
2019-05-18
EGAS00001003658
Epitope-linked Ig-seq of self-reactive plasma cells in celiac disease
Transcriptome Analysis
2019-05-20
EGAS00001003659
Genomic Signatures Reveal DNA Damage Response Deficiency in Brain Metastases of Colorectal Cancer
Other
2019-05-20
EGAS00001003660
Whole-genome and transcriptome sequencing of blastic plasmacytoid dendritic cell neoplasm
Cancer Genomics
2019-05-20
EGAS00001003661
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Other
2019-05-21
EGAS00001003662
Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Other
2019-05-21
EGAS00001003663
Massively parallel single-cell B-cell receptor sequencing enables rapid discovery of diverse antigen-reactive antibodies
Other
2019-05-22
EGAS00001003667
RNA-seq as a tool for evaluating human embryo competence
Other
2019-05-23
EGAS00001003670
Indonesian Genome Diversity Project 2, genotyping data
Other
2019-05-27
EGAS00001003671
Indonesian RNA-seq data
Other
2019-05-27
EGAS00001003672
Molecular Profiling Reveals Unique Immune and Metabolic Features of Melanoma Brain Metastases
Other
2019-05-27
EGAS00001003673
Single-cell TCR sequencing of DQ2.2-glut-L1-specific T cells
Other
2019-05-28
EGAS00001003674
Single-cell TCR sequencing of DQ2.5-hor-3-specific T cells
Other
2019-05-28
EGAS00001003676
Resident memory CD8 T cells persist for years in human small intestine
Other
2019-05-28
EGAS00001003678
Presence of bacterial infection in brains of patients with Huntington's disease (HD)
Other
2019-05-30
EGAS00001003679
Next Generation Sequencing Characterization of Hematopoietic Stem and Progenitors Cells in Human Systemic Lupus Eryhtematosus
RNASeq
2019-05-30
EGAS00001003680
Whole exome sequencing for primary lung adenocarcinoma samples
Other
2019-05-31
EGAS00001003681
Single cell RNA sequencing of lung adenocarcinoma.
Other
2019-05-31
EGAS00001003682
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___WGS
Cancer Genomics
2019-05-31
EGAS00001003684
Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation
Other
2019-05-31
EGAS00001003685
RNA-sequençing of 21 inflammatory hepatocellular adenomas
Other
2019-05-31
EGAS00001003686
Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas
Other
2019-05-31
EGAS00001003687
UAMS Smoldering Myeloma Timeline Cohort
Other
2019-05-31
EGAS00001003688
HSC_population_dynamics___TG001_2_samples
Whole Genome Sequencing
2019-06-03
EGAS00001003689
Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Other
2019-06-04
EGAS00001003690
Analysis of copy number variation landscape of glioma by shallow coverage whole genome sequencing
Other
2019-06-04
EGAS00001003695
Detecting and tracking circulating tumour DNA copy number profiles during first line chemotherapy in oesophagogastric adenocarcinoma
Other
2019-06-05
EGAS00001003696
Whole-exome sequencing of acute erythroid leukemia
Other
2019-06-06
EGAS00001003698
Breast_cancer_topographs
Other
2019-06-07
EGAS00001003699
Integrative and comparative genomic analyses identify clinically relevant groups of pulmonary carcinoids and unveil the supra-carcinoids
Other
2019-06-07
EGAS00001003700
GBM cancer stem cell lines -RNA-seq and WGS data
Other
2019-06-07
EGAS00001003701
Transcriptome Analysis Offers a Comprehensive Illustration of the Genetic Background of Pediatric Acute Myeloid Leukemia
RNASeq
2019-06-08
EGAS00001003702
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Whole Genome Sequencing
2019-06-10
EGAS00001003703
Renal_habitat_WXS
Other
2019-06-10
EGAS00001003705
Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers
Other
2019-06-11
EGAS00001003709
Analysis of the genomic landscape of chemoresistant multiple myeloma
Exome Sequencing
2019-06-11
EGAS00001003710
The 3D evolution of glioma cell populations
Other
2019-06-12
EGAS00001003711
ID1 in glioblastoma
Cancer Genomics
2019-06-13
EGAS00001003714
Infant Glioma Molecular Subtype
Other
2019-06-13
EGAS00001003715
Characterization of patient-derived xenograft models of myxoid liposarcoma either sentitive or resistant to trabectedin
Other
2019-06-13
EGAS00001003719
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Other
2019-06-18
EGAS00001003722
Exome and Whole-Genome Sequencing of Central African Hunter-Gatherers and Agriculturalists
Other
2019-06-19
EGAS00001003723
Cancer and germline exomes consisting of FASTQ paired-end reads from melanoma and lung cancer samples
Other
2019-06-19
EGAS00001003724
RNA-seq consisting of FASTQ paired-end reads from cancer samples
Other
2019-06-19
EGAS00001003725
Human adipose tissue immune cells
Other
2019-06-20
EGAS00001003726
RNA Sequencing of paediatric patients with B lymphoblastic leukemia
Other
2019-06-20
EGAS00001003727
From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle
Other
2019-06-21
EGAS00001003730
Genomic, transcriptomic and epigenomic profiling of GCTB
Other
2019-06-26
EGAS00001003731
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Other
2019-06-26
EGAS00001003732
Measuring minimal residual disease in acute myeloid leukemia with MASQ
Cancer Genomics
2019-06-26
EGAS00001003733
Analysis of mechanisms of CD19- relapse following novel low affinity CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) in a Phase I clinical study in paediatric ALL: CARPALL
Other
2019-06-26
EGAS00001003734
CD3 bispecific antibody-induced cytokine release is dispensable for cytotoxic T cell activity
Transcriptome Analysis
2019-06-26
EGAS00001003735
Gene expression by RNAseq in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Other
2019-06-27
EGAS00001003736
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Other
2019-06-27
EGAS00001003737
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Other
2019-06-28
EGAS00001003738
RNA-seq from human embryonic tissues (additional samples 2018)
Other
2019-06-28
EGAS00001003739
DNA methylation in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Other
2019-06-28
EGAS00001003740
Genomics_of_acral_lentiginous_melanoma
Other
2019-06-28
EGAS00001003743
HSC_population_dynamics___CB002_samples
Whole Genome Sequencing
2019-07-01
EGAS00001003744
Single_cell_HSC_colony_WGS_many_years_post_allogeneic_bone_marrow_transplant
Whole Genome Sequencing
2019-07-01
EGAS00001003745
Reference exome data for Australian Aboriginal populations to support health-based research
Other
2019-07-02
EGAS00001003746
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Other
2019-07-02
EGAS00001003747
Gene expression profile of mesothelial-derived carcinoma-associated fibroblasts
Other
2019-07-03
EGAS00001003748
COMPARE study: participants typed during UK Biobank version 2 array development phase
Other
2019-07-03
EGAS00001003750
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Other
2019-07-05
EGAS00001003751
Single cell transcriptomic analysis of the immune cell compartment in the human small intestine and in Celiac disease
Other
2019-07-05
EGAS00001003753
Dissociation of solid tumour tissues with cold active protease for single-cell RNA-seq minimizes conserved collagenase-associated stress responses
Other
2019-07-08
EGAS00001003754
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___TGS_
Other
2019-07-09
EGAS00001003755
High intensity sequencing of plasma cfDNA and WBC gDNA
Other
2019-07-10
EGAS00001003756
RNA-seq of cultured human hematopoietic stem and progenitor cells from umblical cord blood in cytokine-rich ex vivo culture conditions following sphingolipid modulation
Other
2019-07-10
EGAS00001003760
Genetics and transcriptomes of pediatric B cell precursor leukemia with gain of chromosome 21
Other
2019-07-12
EGAS00001003763
Landscape and significance of multiple mutations in oncogenes.
Other
2019-07-16
EGAS00001003764
WES of mCRC xenografts under cetuximab treatment, placebo or after treatment release
Other
2019-07-17
EGAS00001003765
RNAseq of mCRC xenografts under cetuximab treatment, placebo or after treatment release
Other
2019-07-17
EGAS00001003766
Diverse_outcomes_of_controlled_human_malaria_infection_originate_from_host_intrinsic_immune_variation_and_not_var_gene_switching
Transcriptome Analysis
2019-07-17
EGAS00001003767
IBD-dysplasia
Cancer Genomics
2019-07-18
EGAS00001003768
HSC_population_dynamics___KX004_samples___WGS
Whole Genome Sequencing
2019-07-19
EGAS00001003769
Fresh vs. frozen cell preparations of colorectal cancer single-cell RNA sequencing
RNASeq
2019-07-21
EGAS00001003772
The_Genomic_Advances_in_Sepsis__GAinS__RNA_seq
Other
2019-07-23
EGAS00001003774
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Whole Genome Sequencing
2019-07-25
EGAS00001003775
Whole genome and whole transcriptome sequencing of Hepatosplenic T Cell Lymphoma tumor.
Other
2019-07-26
EGAS00001003776
Targetable ERBB2 Mutations in Neurofibroma/Schwannoma Hybrid Nerve Sheath Tumors
Cancer Genomics
2019-07-26
EGAS00001003778
The whole genome landscape of Burkitt lymphoma subtypes
Other
2019-07-26
EGAS00001003779
Single cell RNA sequencing of 33 primary colorectal cancer
RNASeq
2019-07-28
EGAS00001003780
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases.
Other
2019-07-29
EGAS00001003781
WXS of 147 lung cancer patients treated with immunotherapy
Other
2019-07-30
EGAS00001003784
Polyomavirus-positive Merkel cell carcinoma derived from a trichoblastoma suggests an epithelial origin of Merkel cell carcinoma
Cancer Genomics
2019-08-01
EGAS00001003785
Gene expression from human iPSC derived motor neurons.
Other
2019-08-01
EGAS00001003786
Patient-Derived Lung Cancer Organoid
Other
2019-08-01
EGAS00001003787
The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas
Other
2019-08-01
EGAS00001003789
'KOREAN' never-smoker female adenocarcinoma RNA-seq
Other
2019-08-02
EGAS00001003790
Transcriptional changes in GBM through therapy
Other
2019-08-02
EGAS00001003791
Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer
Other
2019-08-02
EGAS00001003792
Distinct Phenotypes of Human Intrahepatic and Extrahepatic Bile duct Organoids and their Applications for Biliary Disease Modeling
Transcriptome Analysis
2019-08-02
EGAS00001003798
Molecular profiling reclassifies adult astroblastoma into known and clinically distinct tumor entities with frequent MAPK pathway alterations
Cancer Genomics
2019-08-08
EGAS00001003800
Methylation CYLD cutaneous syndrome
Other
2019-08-08
EGAS00001003801
Ulcerative colitis study - WES data
Other
2019-08-09
EGAS00001003802
Ulcerative colitis study - RNAseq data
Other
2019-08-09
EGAS00001003803
Spatial Heterogeneity in CLL
Other
2019-08-09
EGAS00001003804
Comprehensive molecular profiling of high-grade serous ovarian cancer
Other
2019-08-12
EGAS00001003805
Celiac disease meta-analysis
Other
2019-08-13
EGAS00001003806
Integration of intra-sample contextual error modeling for improved detection of somatic mutations
Cancer Genomics
2019-08-13
EGAS00001003809
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Other
2019-08-14
EGAS00001003812
Single cell sequencing: Capturing the origin and dynamics of chromosomal copy-number heterogeneity
Cancer Genomics
2019-08-16
EGAS00001003813
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET)
Other
2019-08-19
EGAS00001003814
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) - Intratumoural immune heterogeneity
Other
2019-08-19
EGAS00001003816
Epigenetic and metabolomic data from type 2 diabetes adolescents
Other
2019-08-19
EGAS00001003817
Functional analysis of GATA2 synonymous mutations
Other
2019-08-20
EGAS00001003818
Lothian Birth Cohort 1921 whole genome sequencing study
Other
2019-08-20
EGAS00001003819
Lothian Birth Cohort 1936 whole genome sequencing study
Other
2019-08-20
EGAS00001003820
Molecular patterns of response and treatment failure after frontline venetoclax combinations in older patients with AML
Other
2019-08-21
EGAS00001003821
Preservation of stemness in high-grade serous ovarian cancer organoids requires low Wnt environment
Other
2019-08-21
EGAS00001003822
Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Other
2019-08-22
EGAS00001003823
Gene_epression_regulation_in_cytokine_induced_immune_cell_states
Gene Regulation Study
2019-08-23
EGAS00001003826
Exome sequencing of Fibromyalgia patients
Other
2019-08-24
EGAS00001003827
eccDNA in maternal plasma
Other
2019-08-26
EGAS00001003828
Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma
Other
2019-08-26
EGAS00001003829
Clonal evolution in myelofibrosis during ruxolitinib therapy
Exome Sequencing
2019-08-26
EGAS00001003830
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer
Other
2019-08-27
EGAS00001003831
Exome sequencing data for 40 cases of alopecia areata and vitiligo
Other
2019-08-27
EGAS00001003832
Delineating intratumoural heterogeneity and neoantigen-directed immune escape in Esophageal Squamous Cell Carcinoma
Other
2019-08-27
EGAS00001003834
Genomic Analysis of Primary Plasma Cell Leukemia reveals Complex Structural Alterations and High Risk Mutational Patterns
Other
2019-08-27
EGAS00001003837
RNA-seq, WGS and WES of Hepatocellular carcinomas, enriched in fibrolamellar carcinomas
Other
2019-08-28
EGAS00001003839
Whole exome sequencing CYLD cutaneous syndrome
Other
2019-08-30
EGAS00001003840
Targeted sequencing CYLD cutaneous syndrome
Other
2019-08-30
EGAS00001003841
RNA sequencing CYLD cutaneous syndrome
Other
2019-08-30
EGAS00001003842
Osteosarcoma mate-pair and RNA-sequencing
Other
2019-09-02
EGAS00001003843
C3 SNPs and outcome after lung transplantation
Other
2019-09-04
EGAS00001003845
A single-cell atlas of human glioma
Other
2019-09-05
EGAS00001003846
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Other
2019-09-05
EGAS00001003847
Longitudinal_profiling_of_the_immune_response_to_Plasmodium_vivax_in_naive_hosts_by_RNA_sequencing
Transcriptome Analysis
2019-09-06
EGAS00001003848
The evolutionary steps from primary to metastatic prostate cancer are largely uncharted, and the ability to use DNA present in body fluids as correlates of aggregate metastatic status is under-examined. We reconstructed phylogenies in ten prostate cancer patients with fatal disease using deep targeted sequencing of the prostate, adjacent and distant organs, as well as plasma, serum, and cerebrospinal fluid at various time points. A total of 163 samples are studied.
Other
2019-09-06
EGAS00001003849
Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA
Transcriptome Analysis
2019-09-06
EGAS00001003850
Discovering genetic causes of optic atrophy syndromes through whole exome sequencing
Other
2019-09-09
EGAS00001003852
Modeling glioblastoma invasion using human brain organoids and single-cell transcriptomics
Other
2019-09-09
EGAS00001003853
Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Other
2019-09-10
EGAS00001003856
Targeted sequencing of patients affected by familial or sporadic Alzheimer's disease
Other
2019-09-10
EGAS00001003857
WES of melanoma tumors treated with combined immune checkpoint blockade
Other
2019-09-10
EGAS00001003860
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Other
2019-09-12
EGAS00001003861
IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Other
2019-09-13
EGAS00001003862
Transcriptome_analysis_of_LCM_samples_
Transcriptome Analysis
2019-09-13
EGAS00001003863
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_TGS
Cancer Genomics
2019-09-13
EGAS00001003870
Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007)
Other
2019-09-16
EGAS00001003872
VIKING Health Study - Shetland
Other
2019-09-17
EGAS00001003875
SG10K_Pilot - Large-scale whole-genome sequencing of three diverse Asian populations in Singapore
Other
2019-09-18
EGAS00001003876
Whole Genome Sequencing Reveals Potential Therapeutic Strategy for Monomorphic Epitheliotropic Intestinal T-cell Lymphoma
Other
2019-09-20
EGAS00001003882
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___LYNCH___WGS
Whole Genome Sequencing
2019-09-20
EGAS00001003883
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Other
2019-09-23
EGAS00001003886
Immunopeptidomics of colorectal cancer organoids reveals a sparse HLA class I neoantigen landscape and no increase in neoantigens with interferon or MEK-inhibitor treatment
Cancer Genomics
2019-09-23
EGAS00001003887
Immuno-genomic landscape of osteosarcoma
Other
2019-09-23
EGAS00001003888
RNAseq_of_Human_Organoid_Lines
Cancer Genomics
2019-09-23
EGAS00001003889
Studying the single cell characteristics of pancreatic cancer
Other
2019-09-24
EGAS00001003890
Oesophageal_Adenocarcinoma_Organoid_ATAC
Cancer Genomics
2019-09-25
EGAS00001003892
Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer
Other
2019-09-26
EGAS00001003893
Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes
Other
2019-09-26
EGAS00001003895
Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Other
2019-09-27
EGAS00001003896
Epigenome wide DNA methylation assay of gingivo-buccal oral squamous cell carcinoma using single base resolution high throughput array
Other
2019-09-27
EGAS00001003897
Single-cell T-cell receptor sequencing of intraepithelial gammadelta T-cells in celiac disease
Other
2019-09-27
EGAS00001003899
Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Other
2019-09-27
EGAS00001003901
Screening of 2.5 million SNPs in 142 samples from the western Mediterranean area
Other
2019-09-29
EGAS00001003917
Human Biofluid RNA Atlas Project - raw data
RNASeq
2019-09-30
EGAS00001003922
Meisal temporal lobe epilepsy sequencing study
Other
2019-09-30
EGAS00001003923
WES of 2 human osteosarcoma and corresponding cell lines
Other
2019-10-01
EGAS00001003928
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Other
2019-10-02
EGAS00001003931
Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Other
2019-10-02
EGAS00001003932
Polymorphisms in the mitochondrial genome are associated with bullous pemphigoid in Germans
Other
2019-10-03
EGAS00001003933
ImmunoAgeing_Colonies
Other
2019-10-03
EGAS00001003934
Mutational signature in colorectal cancer induced by genotoxic pks+ E. coli
Other
2019-10-04
EGAS00001003941
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Other
2019-10-07
EGAS00001003942
Deep intronic homozygous variation in PSMC3 causes a syndromic neurosensory disorder combining deafness and cataract
Other
2019-10-07
EGAS00001003944
Description and determinants of the faecal resistome and microbiome of farmers and slaughterhouse workers: a metagenome-wide cross-sectional study.
Other
2019-10-08
EGAS00001003946
Natural Killer Cell Plasticity During IL-15-driven Homeostatic Proliferation
Other
2019-10-08
EGAS00001003949
Molecular profiling of DLBCL patients treated in the HOVON84 trial
Other
2019-10-10
EGAS00001003950
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Other
2019-10-10
EGAS00001003951
CRISPR-based adenine editors correct nonsense mutations in a cystic fibrosis organoid biobank.
Whole Genome Sequencing
2019-10-10
EGAS00001003952
Targeted_sequencing_of_embryonic_variants___Warm_Autopsy
Cancer Genomics
2019-10-10
EGAS00001003953
Glioblastoma epigenome profiling identifies SOX10 as a master regulator of molecular tumour subtype
Other
2019-10-10
EGAS00001003955
Genomic landscape of signals of positive natural selection in North Eurasia
Other
2019-10-14
EGAS00001003958
genome-wide cfDNA methylation analysis
Other
2019-10-15
EGAS00001003962
Breast implant-associated anaplastic large cell lymphoma shallow whole genome sequencing for copy number analysis and Whole exome sequencing data.
Other
2019-10-17
EGAS00001003963
Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring
Other
2019-10-17
EGAS00001003964
Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing
Other
2019-10-17
EGAS00001003967
STRATAA_RNAseq
Other
2019-10-18
EGAS00001003968
Intellectual Disability cases with parents (trios) or affected sibs (sibpairs)
Other
2019-10-18
EGAS00001003970
Whole-exome sequencing of intravascular large B-Cell lymphoma
Other
2019-10-18
EGAS00001003973
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Other
2019-10-20
EGAS00001003974
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Other
2019-10-21
EGAS00001003975
Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia
Other
2019-10-22
EGAS00001003976
Phenotypic_characterisation_of_LRRN4CL_over_expression
Transcriptome Analysis
2019-10-23
EGAS00001003979
Activation of IL7RA signalling in human B-lymphoid precursors induces pre-leukemia
Cancer Genomics
2019-10-24
EGAS00001003980
Molecular Profiles of BRCA1-Associated Ovarian Cancer Treated by Platinum-Based Therapy
Cancer Genomics
2019-10-25
EGAS00001003981
Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification
Other
2019-10-25
EGAS00001003982
Increased mutation accumulation during fetal development in Down syndrome
Other
2019-10-28
EGAS00001003984
SCLC ctDNA sequencing
Other
2019-10-28
EGAS00001003985
SCLC tumor sequencing
Other
2019-10-28
EGAS00001003986
Investigation of relapse prediction in infants with MLL-rearranged Acute Lymphoblastic Leukemia
Other
2019-10-28
EGAS00001003987
SCC ctDNA sequencing
Other
2019-10-28
EGAS00001003988
SCC tumor sequencing
Other
2019-10-28
EGAS00001003989
circulating-tumor DNA sequencing of healthy samples
Other
2019-10-28
EGAS00001003991
MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Other
2019-10-28
EGAS00001003992
Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas.
Other
2019-10-29
EGAS00001003993
Peripheral clonal expansion of T cells (scRNA-seq)
RNASeq
2019-10-29
EGAS00001003994
Peripheral clonal expansion of T cells (scTCR-seq)
Other
2019-10-29
EGAS00001003996
A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart
Other
2019-10-29
EGAS00001003997
InsPIRE islets
Other
2019-10-30
EGAS00001003999
Myeloma RNAseq
RNASeq
2019-10-31
EGAS00001004000
Myeloma WGS
Other
2019-10-31
EGAS00001004001
Tumor-specific expression of let-7i and miR-192 is associated with resistance to cisplatin-based chemoradiotherapy in patients with larynx and hypopharynx cancer
Other
2019-11-01
EGAS00001004003
SSBP1
Other
2019-11-02
EGAS00001004006
Genomic and immune profiling of pre-invasive lung adenocarcinoma
Other
2019-11-04
EGAS00001004007
Whole-genome sequencing of normal Singaporean volunteers
Other
2019-11-04
EGAS00001004008
Single cell RNAseq of PBMC from bladder cancer patients
Other
2019-11-04
EGAS00001004009
Spontaneous mutations in the single TTN gene represent high tumor mutation burden
Other
2019-11-05
EGAS00001004012
Familial adult myoclonic epilepsy in Sri Lankan and Indian families
Other
2019-11-06
EGAS00001004013
Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Other
2019-11-06
EGAS00001004014
Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking
Other
2019-11-06
EGAS00001004015
Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma.
Other
2019-11-06
EGAS00001004016
Epigenomic data of HEMa_LP
Other
2019-11-07
EGAS00001004018
A Protein Neddylation Inhibitor MLN4924 Suppresses Patient-Derived Glioblastoma Cells via Inhibition of ERK and AKT Signaling
Other
2019-11-08
EGAS00001004019
Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project
Other
2019-11-08
EGAS00001004020
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Other
2019-11-08
EGAS00001004022
Berlin Neuroblastoma Dataset
Cancer Genomics
2019-11-09
EGAS00001004023
Multi-regional tumour biopsies of a RET fusion patient
Other
2019-11-11
EGAS00001004026
Whole exome sequencing from early stage non-small cell lung cancer patients at MDACC
Other
2019-11-13
EGAS00001004027
Tumor intrinsic and extrinsic mechanisms of response and resistance to blinatumomab in relapsed/refractory acute lymphoblastic leukemia
Other
2019-11-13
EGAS00001004028
Exome Sequencing of Spanish Patients with rare genetic diseases.
Other
2019-11-14
EGAS00001004030
Single-cell analysis reveals fibroblast clusters linked to immunotherapy resistance in cancer
Other
2019-11-15
EGAS00001004031
RNA-seq data from iCAF (sorted) and myCAF cluster 0 (spread) CAF-S1 fibroblasts maintained in culture
Other
2019-11-15
EGAS00001004032
RNA-seq data from Non Small Cell Lung Cancer (NSCLC) samples
Other
2019-11-15
EGAS00001004033
UCSF Pediatric Bithalamic Glioma Genome Project
Other
2019-11-17
EGAS00001004034
GRIDSS, PURPLE, LINX: Unscrambling the tumor genome via integrated analysis of structural variation and copy number
Other
2019-11-18
EGAS00001004035
Single Cell Sperm sequencing try 2
Other
2019-11-18
EGAS00001004036
Genomic insight into the origins and dispersal of the Brazilian Coastal Natives
Population Genomics
2019-11-18
EGAS00001004042
Human Pancreatic Islet RNAseq - Lund
Other
2019-11-19
EGAS00001004043
Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy
Other
2019-11-20
EGAS00001004044
GWAS data on human pancreatic islets from 191 donors - Lund
Other
2019-11-20
EGAS00001004050
Neoantigen responses to Immunotherapy in Prostate Cancer
Other
2019-11-21
EGAS00001004051
Oesophageal_Adenocarcinoma_Organoids_Iso_Seq
Cancer Genomics
2019-11-21
EGAS00001004053
Cell type-specific transcriptomics of esophageal adenocarcinoma as a scalable alternative for single cell transcriptomics
Other
2019-11-22
EGAS00001004055
Concurrent germline and somatic pathogenic BAP1 variants in a patient with metastatic bladder cancer
Cancer Genomics
2019-11-25
EGAS00001004056
Phenotyping data on human pancreatic islets from 191 donors - Lund
Other
2019-11-25
EGAS00001004059
Expression profiles and genetic makeup of metastases of a cancer of unknown primary.
Cancer Genomics
2019-11-26
EGAS00001004063
Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles
Other
2019-11-27
EGAS00001004064
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Other
2019-11-27
EGAS00001004066
Bottleneck_Sequencing_Of_Human_Tissue__Wgs_
Cancer Genomics
2019-11-27
EGAS00001004069
HCA_Placenta_Adult_Vento_RNA
Other
2019-11-27
EGAS00001004070
single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes
Other
2019-11-29
EGAS00001004071
RNA-seq study of longitudinal blood cell samples from children at risk of type 1 diabetes
Other
2019-11-29
EGAS00001004074
Neoadjuvant combination PD-L1 plus CTLA-4 blockade in patients with cisplatin-ineligible operable urothelial carcinoma
Other
2019-12-02
EGAS00001004075
The Jerusalem Perinatal Study (JPS) aimed to examine the developmental origins of cardiometabolic risk.
Other
2019-12-03
EGAS00001004076
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Other
2019-12-03
EGAS00001004077
Whole exome sequencing study for 8 pairs of primary NSCLCs and distant metastases
Other
2019-12-03
EGAS00001004078
RNA sequencing study for 8 pairs of primary NSCLCs and distant metastases
Other
2019-12-03
EGAS00001004079
DNA methylation array study for 7 pairs of primary NSCLCs and distant metastases
Other
2019-12-03
EGAS00001004080
End structure of DNA in plasma: detection, characterizationand diagnostic applications
Other
2019-12-04
EGAS00001004081
RNA sequencing of CD8 T cells from melanoma patients prior to and during checkpoint immunotherapy and untreated healthy controls
Other
2019-12-04
EGAS00001004082
Single cell RNA-seq mapping of nasal and tracheobronchial airways in human healthy volunteers
Other
2019-12-04
EGAS00001004084
Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis.
Exome Sequencing
2019-12-04
EGAS00001004085
Single-cell RNA sequencing of 22 Hodgkin lymphoma tumors and 5 reactive lymph nodes
Other
2019-12-04
EGAS00001004086
Whole exome sequencing of advanced gastric cancer
Other
2019-12-05
EGAS00001004087
Multiple Sclerosis risk variants regulate gene expression in innate and adaptive immune cells
Other
2019-12-05
EGAS00001004088
Rapid response of APC/TP53/KRAS mutated stage IV colorectal cancer under FOLFIRI + Bevacizumab detected by liquid biopsy: a case report
Other
2019-12-05
EGAS00001004089
HCA_Adrenal_Foetal_WSSS_RNA_SB
Transcriptome Analysis
2019-12-05
EGAS00001004090
HNSCC RNA-seq
RNASeq
2019-12-05
EGAS00001004091
HNSCC copy number alterations
Whole Genome Sequencing
2019-12-05
EGAS00001004092
Mitochondrial DNA sequencing in samples of Huntington’s disease patients
Other
2019-12-05
EGAS00001004093
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Other
2019-12-06
EGAS00001004097
Evolutionary Origins of Recurrent Pancreatic Cancer
Other
2019-12-07
EGAS00001004102
SDH_deficient_renal_tumours___WGS_
Other
2019-12-09
EGAS00001004103
SDH_deficient_renal_tumours___RNA_
Other
2019-12-09
EGAS00001004106
Comprehensive pharmacogenomic characterization of gastric cancer
Other
2019-12-11
EGAS00001004107
Single cell RNA seq of the developing human embryo brain
Other
2019-12-11
EGAS00001004108
54 metastatic colorectal cancer patients from Schleswig-Holstein in North Germany
Other
2019-12-11
EGAS00001004110
Exon4-mutations in KRAS Affect MEK-ERK and Pi3K-AKT Signaling in Multiple Myeloma
Other
2019-12-12
EGAS00001004111
Y chromosome variability in Polish population
Other
2019-12-12
EGAS00001004112
Reference Exome Data for a Northern Brazilian population
Other
2019-12-13
EGAS00001004113
Lenalidomide Resistance in del(5q) Myelodysplastic Syndrome Follows Loss of RUNX1/TP53-mediated Megakaryocytic Differentiation
Other
2019-12-13
EGAS00001004114
White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Other
2019-12-15
EGAS00001004115
Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients
Whole Genome Sequencing
2019-12-16
EGAS00001004116
CD8+ T-cell exhaustion induced by leukemic cells drives progression in Chronic Lymphocytic Leukemia
Other
2019-12-16
EGAS00001004117
Genomic landscape of inflammatory breast cancer by whole-genome sequencing
Other
2019-12-16
EGAS00001004118
Imaging metabolic heterogeneity in breast cancer using hyperpolarized 13C-MRI
Other
2019-12-16
EGAS00001004122
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___MAP___WGS
Cancer Genomics
2019-12-17
EGAS00001004123
Benchmarking of ProSolo, a new probabilistic single nucleotide variant caller for single cell DNA sequencing data. This study provides the whole exome sequencing dataset used in this assessment.
Other
2019-12-18
EGAS00001004124
Genomic_characterisation_of_MGUS__
Cancer Genomics
2019-12-18
EGAS00001004126
Germline elongator mutations in sonic hedgehog medulloblastoma
Other
2019-12-19
EGAS00001004127
RNASeq for BMI GL study
RNASeq
2019-12-23
EGAS00001004135
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Other
2020-01-07
EGAS00001004136
Phased whole genome sequencing of 10 melanoma samples
Other
2020-01-07
EGAS00001004139
Amplicon based NGS of human CD4 and CD8 T cells
Other
2020-01-08
EGAS00001004145
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
Other
2020-01-09
EGAS00001004147
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Gene Regulation Study
2020-01-10
EGAS00001004151
Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Other
2020-01-10
EGAS00001004152
Transcriptomic signatures of CD4+ T cells from visceral leishmaniasis (VL) patients
Other
2020-01-13
EGAS00001004153
The miR-185/PAK6 Axis Predicts Therapy Response and Regulates Survival of Drug-Resistant Leukemic Stem Cells in Chronic Myeloid Leukemia
Other
2020-01-13
EGAS00001004156
FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Cancer Genomics
2020-01-15
EGAS00001004157
Metastatic Adult Pancreatoblastoma: Multimodal Treatment and Molecular Characterization of a Very Rare Disease (NCT MASTER)
Other
2020-01-15
EGAS00001004160
Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers
Other
2020-01-17
EGAS00001004165
Genomic and epigenomic insights into the origin, pathogenesis and clinical behavior of mantle cell lymphoma subtypes
Other
2020-01-19
EGAS00001004168
High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations
Other
2020-01-20
EGAS00001004169
Chromatin run-on and RNA sequencing of fibrolamellar carcinoma
Other
2020-01-20
EGAS00001004175
Whole-exome sequencing of the transposition of the great arteries
Other
2020-01-21
EGAS00001004176
Two monogenic disorders masquerading as one: Severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss
Exome Sequencing
2020-01-22
EGAS00001004177
The role of the mammalian SWI/SNF chromatin remodeling complex in neuroendocrine prostate cancer
Other
2020-01-22
EGAS00001004181
JAK and STAT alterations in CD30 positive LPD
Cancer Genomics
2020-01-22
EGAS00001004182
Targeted sequencing of breast cancers with germline BRCA1/2 mutations
Other
2020-01-22
EGAS00001004186
Prostate Cancer mitochondrial DNA heteroplasmies and mitochondrial gene expression
Cancer Genomics
2020-01-25
EGAS00001004187
Vento_Placental_Cell_Atlas
Other
2020-01-27
EGAS00001004189
Integrative molecular analysis of pediatric Anaplastic large cell lymphoma reveals subtypes with distinct immune suppression signatures.
Other
2020-01-27
EGAS00001004192
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Other
2020-01-29
EGAS00001004193
HSC_population_dynamics___KX007_samples
Cancer Genomics
2020-01-29
EGAS00001004194
cfRRBS on cfDNA from pediatric cancer
Other
2020-01-30
EGAS00001004196
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Other
2020-01-31
EGAS00001004197
Immuno-genomic landscape of osteosarcoma
Other
2020-01-31
EGAS00001004199
Gene expression in brain (Schizophrenia) study
Other
2020-02-03
EGAS00001004200
High coverage sequencing of a single sample can account for the problem of intratumor heterogeneity
Exome Sequencing
2020-02-03
EGAS00001004201
StemNet - in vitro differentiation of human hepatocytes
Other
2020-02-03
EGAS00001004203
Genetics and transcriptomics of human acute erythroid leukemia
Cancer Genomics
2020-02-05
EGAS00001004204
Whole exome sequencing in familial Multiple Sclerosis
Other
2020-02-05
EGAS00001004207
Sex-biased patterns shaped the genetic history of Roma
Other
2020-02-06
EGAS00001004208
Pancreatic tropism of metastatic renal cell carcinoma
Other
2020-02-06
EGAS00001004209
Native American gene flow into Polynesia predating Easter Island settlement
Other
2020-02-07
EGAS00001004210
HCA_Female_Reporductive_Adult_WSSS_RNA
Other
2020-02-07
EGAS00001004211
Association of DNA-methylation profiles with immune responses in breast cancer patients
Epigenetics
2020-02-07
EGAS00001004212
The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Other
2020-02-09
EGAS00001004213
Real-time response profiling through serial plasma analyses during FOLFOX treatment in patients with colorectal cancer
Other
2020-02-10
EGAS00001004214
Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Other
2020-02-10
EGAS00001004216
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Other
2020-02-10
EGAS00001004218
HDAC3 mediates the inflammatory response and LPS tolerance in human monocytes and macrophages
RNASeq
2020-02-12
EGAS00001004220
KDM4A regulates the maternal-to-zygotic transition by protecting broad H3K4me3 domains from H3K9me3 invasion in oocytes
Transcriptome Analysis
2020-02-12
EGAS00001004221
Whole-genome DNA methylation profiling of CD14+ monocytes reveals disease status and activity differences in Crohn’s disease patients
Other
2020-02-12
EGAS00001004224
CYPTAM - PacBio SMRT sequencing
Other
2020-02-12
EGAS00001004228
Heterogeneous Genomic Evolution and Immune Microenvironments in Metastatic Lung Cancer
Other
2020-02-14
EGAS00001004229
NanoSring of PBMC from bladder cancer and RCC patients
Other
2020-02-14
EGAS00001004230
Single Cell RNAseq of blood and tumor from renal cancer patients
Other
2020-02-14
EGAS00001004231
Whole exome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Exome Sequencing
2020-02-16
EGAS00001004232
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Other
2020-02-16
EGAS00001004233
Single-cell RNA sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Other
2020-02-16
EGAS00001004235
Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
Other
2020-02-18
EGAS00001004237
The_Little_Princess_Knowledge_Bank_
Cancer Genomics
2020-02-18
EGAS00001004238
iNeuron_RNAseq
Other
2020-02-18
EGAS00001004239
: Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumours
Cancer Genomics
2020-02-18
EGAS00001004241
Spinocerebellar ataxia type 3 RNA-sequencing study
Other
2020-02-19
EGAS00001004242
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Other
2020-02-19
EGAS00001004243
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Other
2020-02-19
EGAS00001004248
Whole-exome sequencing of ovarian clear cell carcinoma in clinical outliers
Other
2020-02-21
EGAS00001004249
Adult granulosa cell tumor WGS data cohort with corresponding reference germline WGS data
Other
2020-02-21
EGAS00001004250
The landscape of chromothripsis across adult cancer types
Other
2020-02-21
EGAS00001004255
Single cell RNA-seq profiling of CD8 T cells from elder adults
Other
2020-02-24
EGAS00001004266
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Other
2020-02-27
EGAS00001004267
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Other
2020-02-27
EGAS00001004268
Bone metastatic biopsies of breast cancer patients progressing on endocrine therapies.
Cancer Genomics
2020-02-28
EGAS00001004270
CHD8 RNAseq
RNASeq
2020-02-28
EGAS00001004271
Genome-wide study of the effect of blood collection tubes on the cell-free DNA methylome
Other
2020-02-28
EGAS00001004272
Genetic characterization of a Unique Neuroendocrine Transdifferentiation Prostate Circulating Tumor Cell - Derived eXplant (CDX) Model
Cancer Genomics
2020-02-28
EGAS00001004273
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Other
2020-02-29
EGAS00001004274
Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair
Other
2020-03-02
EGAS00001004275
Multiplexed quantification of four neuroblastoma DNA targets in a single droplet digital PCR reaction
Other
2020-03-02
EGAS00001004276
Longitudinal therapy monitoring of ALK-positive non-small cell lung cancer (copy number, cell-free DNA)
Other
2020-03-02
EGAS00001004277
Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Other
2020-03-02
EGAS00001004280
ImmunoAgeing_Colonies_WGS
Other
2020-03-03
EGAS00001004281
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Other
2020-03-03
EGAS00001004282
Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Other
2020-03-03
EGAS00001004283
Ensemble learning for classifying single-cell data and projection across reference atlases
Other
2020-03-03
EGAS00001004284
The impact of urbanization and diet on innate immune responses in healthy Tanzanians
RNASeq
2020-03-03
EGAS00001004285
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Other
2020-03-03
EGAS00001004286
Total RNAseq in the sporadic ALS and healthy control motor cortex
Other
2020-03-04
EGAS00001004287
Roma Sequencing Study
Other
2020-03-04
EGAS00001004288
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma
Exome Sequencing
2020-03-04
EGAS00001004289
Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Other
2020-03-04
EGAS00001004290
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-009
Other
2020-03-05
EGAS00001004291
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-010
Other
2020-03-05
EGAS00001004292
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC-- CA209-025
Other
2020-03-05
EGAS00001004293
MethCORR: DNA Methylation-based Characterization, Classification and Prognostication of Colorectal Cancer using Archival Formalin-fixed, Paraffin-embedded Tissue
Other
2020-03-05
EGAS00001004296
Molecular profiling of metastatic uveal melanoma
Other
2020-03-05
EGAS00001004298
IgCaller
Other
2020-03-09
EGAS00001004301
H3.3G34R/V-transformed interneuron progenitors co-opt PDGFRA for gliomagenesis
Other
2020-03-09
EGAS00001004303
Egyptref: An integrated personal and population-based Egyptian genome reference
Other
2020-03-10
EGAS00001004311
Healthy_ageing_thymus
Other
2020-03-12
EGAS00001004312
PFA ependymoma cancer study
Other
2020-03-14
EGAS00001004314
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Other
2020-03-19
EGAS00001004315
Enhancer-gene rewiring in the pathogenesis of Quebec Platelet Disorder
Epigenetics
2020-03-19
EGAS00001004316
Hereditary Cancer Diagnostics with I2HCP gene panel
Other
2020-03-20
EGAS00001004319
Long-read trio sequencing of unsolved patients with intellectual disability
Other
2020-03-24
EGAS00001004320
Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.
Cancer Genomics
2020-03-24
EGAS00001004322
Rare_renal_tumours_WGS_
Other
2020-03-25
EGAS00001004323
Rare_renal_tumours_RNA_
Other
2020-03-25
EGAS00001004325
Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia
Other
2020-03-26
EGAS00001004326
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Other
2020-03-26
EGAS00001004327
METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation
Other
2020-03-27
EGAS00001004328
Activating AKT1 and PIK3CA mutations in metastatic castration-resistant prostate cancer
Cancer Genomics
2020-03-27
EGAS00001004329
Genomic_landscape_of_liver_cirrhosis
Other
2020-03-29
EGAS00001004332
Whole-genome and transcriptome sequencing of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma
Other
2020-04-03
EGAS00001004335
Dissecting intratumor heterogeneity of nodal B cell lymphoma on the transcriptional, genetic, and drug response level
Other
2020-04-06
EGAS00001004338
Umbrella Study of MASTER/H021 data (not to be released, pool)
Cancer Genomics
2020-04-06
EGAS00001004340
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Other
2020-04-14
EGAS00001004341
Comprehensive molecular characterization of brainstem glioma
Other
2020-04-14
EGAS00001004342
Plasma DNA profile in DNASE1L3 deficiency
Other
2020-04-15
EGAS00001004343
Molecular determinants of response to PD-L1 blockade across tumor types
Other
2020-04-15
EGAS00001004344
A molecular cell atlas of the human lung from single cell RNA sequencing
Other
2020-04-15
EGAS00001004345
Multi-omics profiling of paired primary and recurrent glioblastoma patient tissues
Other
2020-04-16
EGAS00001004346
Whole genome bisulfite sequencing on 10 multiple myeloma cases
Other
2020-04-16
EGAS00001004347
RNAseq on 20 samples of multiple myeloma patients and 3 normal plasma cells.
Other
2020-04-16
EGAS00001004348
Enhanced reduced representation bisulfite sequencing (eRRBS) on 45 multiple myeloma samples and 3 normal plasma cell
Other
2020-04-16
EGAS00001004349
Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Other
2020-04-16
EGAS00001004352
Epigenomic profile of diverse cancer
Other
2020-04-17
EGAS00001004353
Molecular subsets in renal cancer determine outcome to checkpoint and angiogenesis blockade
Other
2020-04-17
EGAS00001004355
Cell-free DNA fragmentation patterns and personalized sequencing reveal circulating tumor DNA in urine and plasma of glioma patients
Other
2020-04-20
EGAS00001004356
Phylogenetic reconstruction of breast cancer
Other
2020-04-20
EGAS00001004357
Whole-exome sequencing of extranodal NK/T cell lymphoma
Other
2020-04-20
EGAS00001004358
RNA-sequencing of Non-muscle Invasive Bladder cancer (NMIBC)
Other
2020-04-20
EGAS00001004359
Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma
Other
2020-04-20
EGAS00001004361
TP53 variant detection analysis in high grade serous epithelial ovarian cancer
Other
2020-04-21
EGAS00001004362
Genetic diversity and continuity of the population of the UAE
Other
2020-04-21
EGAS00001004363
Comprehensive Genomic Characterization of Refractory Multiple Myeloma Reveals a Complex Mutational and Structural Landscape Associated with Drug Resistance (H067)
Other
2020-04-21
EGAS00001004364
Whole-genome sequencing of rare disease patients in a national healthcare system
Other
2020-04-21
EGAS00001004365
Candidate Gene Case Control Study of Human African Trypanosomiasis in the Democratic Republic of Congo
Other
2020-04-21
EGAS00001004366
Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome
Other
2020-04-21
EGAS00001004367
Skeletal muscle transcriptomic comparison between long-term trained and untrained men and women
Other
2020-04-22
EGAS00001004369
scRNA-seq data of BALF and blood cells from COPD and control
Other
2020-04-22
EGAS00001004370
Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Other
2020-04-22
EGAS00001004371
Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Other
2020-04-22
EGAS00001004373
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
Other
2020-04-23
EGAS00001004374
Single cell characterization of arrested B-lymphoid differentiation and leukemic cell states in ETV6-RUNX1-positive pediatric leukemia
RNASeq
2020-04-23
EGAS00001004375
RNA-seq of human embryonic heart, lung, and cerebellum
Other
2020-04-23
EGAS00001004376
OSCC WES + WGS Boot et al. 2020
Cancer Genomics
2020-04-24
EGAS00001004379
Whole genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes
Other
2020-04-26
EGAS00001004380
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Other
2020-04-27
EGAS00001004381
scRNA-seq of HSPC treated with gemcitabine and carbplatin
Other
2020-04-27
EGAS00001004383
Matching of actionable mutations with therapies in cancer patients: comparison of three commercial decision support platforms
Other
2020-04-28
EGAS00001004386
Bulk RNAseq gene expression of baseline tumors from metastatic urothelial bladder cancer patients (IMvigor210) and metastatic renal cell carcinoma (IMmotion150)
Other
2020-04-28
EGAS00001004388
Neuroblastoma and adrenal gland single-cell study
Other
2020-04-29
EGAS00001004390
Subtype specific studies of breast cancer progression. Milan cohort.
Other
2020-04-30
EGAS00001004391
Paediatric_and_adult_nasal_RNAseq___COVID19
Transcriptome Analysis
2020-04-30
EGAS00001004392
Genomic study of an AT-AML
Other
2020-04-30
EGAS00001004394
Genome sequencing of oesophagus atresia families
Other
2020-04-30
EGAS00001004395
glioblastoma and glioblastoma stem cells (GSCs), RNA-seq and WGS
Other
2020-04-30
EGAS00001004396
Detailed molecular and immune marker profiling of archival prostate cancer samples
Cancer Genomics
2020-04-30
EGAS00001004397
GBM stem cell lines and PRMT5 inhibitor
Cancer Genomics
2020-04-30
EGAS00001004401
H3Africa - Respiratory Microbiota of African Children
Other
2020-05-05
EGAS00001004402
Transcriptomic analysis of Acute Myeloid Leukemia stem cells
Other
2020-05-05
EGAS00001004404
Accelerated single cell seeding in relapsed multiple myeloma
Cancer Genomics
2020-05-05
EGAS00001004405
Homologous recombination DNA repair deficiency and PARP inhibition activity in primary triple negative breast cancer
Other
2020-05-06
EGAS00001004406
Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring
Other
2020-05-06
EGAS00001004407
Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia
Other
2020-05-07
EGAS00001004408
Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association method
Other
2020-05-08
EGAS00001004409
Plasma DNA profile in DNASE1L3 deficiency-Mouse AAV samples
Other
2020-05-08
EGAS00001004410
Scottish High Grade Serous Ovarian Cancer
Other
2020-05-08
EGAS00001004412
Potent neutralizing antibodies against SARS-CoV-2
Other
2020-05-09
EGAS00001004413
Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients
Other
2020-05-11
EGAS00001004415
WES
Other
2020-05-11
EGAS00001004416
expression
Other
2020-05-11
EGAS00001004418
STM4 - Mouliere et al, 2018. Enhanced detection of circulating tumor DNA by fragment size analysis
Cancer Genomics
2020-05-11
EGAS00001004419
SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells
Other
2020-05-12
EGAS00001004420
Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Other
2020-05-12
EGAS00001004422
Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Other
2020-05-13
EGAS00001004424
RA-Map, A multi-omic survey of whole blood and subsets in early rheumatoid arthritis and vaccine study controls
Other
2020-05-13
EGAS00001004428
Performance assessment of Total RNA sequencing of human biofluids and extracellular vesicles
RNASeq
2020-05-14
EGAS00001004429
The genomic landscape of primary cutaneous anaplastic large cell lymphoma (pcALCL)
Other
2020-05-15
EGAS00001004430
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Cancer Genomics
2020-05-15
EGAS00001004431
Dual-mTOR inhibitor Rapalink-1 reduces prostate cancer patient-derived xenograft growth and alters tumor heterogeneity
Other
2020-05-16
EGAS00001004434
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort
Other
2020-05-19
EGAS00001004435
DO NOT USE - Whole genome sequencing of SI-NETs from five patients
Other
2020-05-19
EGAS00001004436
Highlighted samples from the BCH CRDC
Other
2020-05-19
EGAS00001004437
Deep sequencing of the gut microbiome from 946 healthy donors of the Milieu Intérieur cohort
Other
2020-05-20
EGAS00001004438
Immunogenomics of colorectal cancer response to immune checkpoint blockade
Other
2020-05-20
EGAS00001004439
Patient-derived organoids as a novel tool to study cervical cancer
Other
2020-05-21
EGAS00001004440
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Other
2020-05-21
EGAS00001004443
Single-cell analysis for metastatic gastric adenocarcinoma
Other
2020-05-21
EGAS00001004444
Immunogenomic landscape of hematological malignancies
Other
2020-05-21
EGAS00001004445
Clinical efficacy and biomarker analysis of neoadjuvant atezolizumab in operable urothelial carcinoma in the ABACUS trial
Other
2020-05-22
EGAS00001004446
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Breast cohort
Other
2020-05-22
EGAS00001004447
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Lung cohort
Other
2020-05-22
EGAS00001004448
Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Other
2020-05-22
EGAS00001004449
Single cell sequencing in CNS autoimmune disease
RNASeq
2020-05-23
EGAS00001004451
Single cell RNAseq of PBMC from RCC patients
Other
2020-05-24
EGAS00001004452
FOXM1 is a biomarker of resistance to PI3Kα inhibition in ER+ breast cancer that is detectable using metabolic imaging (RNA-seq data)
Other
2020-05-24
EGAS00001004454
A molecular signature for IL-10-producing Th1 cells in protozoan parasitic diseases
Other
2020-05-26
EGAS00001004455
CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase
Other
2020-05-26
EGAS00001004456
Comparative analysis of somatic variant calling on matched FF and FFPE WGS samples
Other
2020-05-26
EGAS00001004458
Single cell RNAseq of PBMC from bladder cancer patients
Other
2020-05-27
EGAS00001004459
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Other
2020-05-28
EGAS00001004460
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Other
2020-05-29
EGAS00001004461
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas
Other
2020-05-30
EGAS00001004462
Mutational_burden_in_human_hair_follicles
Cancer Genomics
2020-06-01
EGAS00001004463
Immunoreactive_p53_areas_in_human_skin_2
Cancer Genomics
2020-06-01
EGAS00001004464
_WGS__Somatic_mutation_in_skin_epidermis__SMS_
Cancer Genomics
2020-06-01
EGAS00001004465
WGS_skin_punches
Cancer Genomics
2020-06-01
EGAS00001004466
Single cell RNA sequencing of normal endometrial derived organoids uncovers novel cell type markers for prognostication
Other
2020-06-01
EGAS00001004467
Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001
Other
2020-06-01
EGAS00001004468
A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma
Other
2020-06-02
EGAS00001004470
Defective mitophagy and enhanced oxidative stress dictate regulatory T cell impairment in autoimmunity
Other
2020-06-02
EGAS00001004472
Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups
Other
2020-06-03
EGAS00001004473
Evolutionary analysis of pancreatic neoplastic cysts through whole-exome and targeted sequencing
Other
2020-06-03
EGAS00001004476
RNA sequencing of subchondral bone from patients that underwent a joint replacement surgery due to osteoarthritis.
RNASeq
2020-06-04
EGAS00001004477
Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung
Other
2020-06-04
EGAS00001004478
Identifying the role of ID3 in DNA repair and maintenance of genome integrity
Other
2020-06-09
EGAS00001004479
Profiling the unique protective properties of intracranial arterial endothelial cells
Other
2020-06-09
EGAS00001004480
The gut microbiota in prediabetes and diabetes: a population-based cross-sectional study
Other
2020-06-10
EGAS00001004481
Single-cell analysis of airway samples identifies immune cell activation correlating with COVID-19 disease severity
Other
2020-06-10
EGAS00001004482
Mutational Landscape of Grey Zone Lymphoma
Other
2020-06-10
EGAS00001004484
Single-cell sequencing of gammadelta and CD8+ alphabeta TCR sequences from blood and gut in coeliac disease
Other
2020-06-11
EGAS00001004485
EORTC RP1335 SPECTA Lung cancer data
Other
2020-06-12
EGAS00001004486
Whole exome sequencing of long-term, never relapse exceptional responders of trastuzumab-treated HER2+ metastatic breast cancer
Other
2020-06-12
EGAS00001004489
Autoimmunity_and_immunodeficiency_COVID19
Other
2020-06-16
EGAS00001004490
HSC_population_dynamics___KX008_samples
Whole Genome Sequencing
2020-06-16
EGAS00001004491
A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients
Other
2020-06-16
EGAS00001004492
Fine-Scale Genomic Analyses Of Admixed Individuals Reveal Unrecognized Genetic Ancestry Components In Argentina
Other
2020-06-17
EGAS00001004494
Cabozantinib Response in ETV6-NTRK3 G623R Positive Carcinoma HIPO-021
Other
2020-06-18
EGAS00001004495
Targets of MEK inhibition in DIPG
Other
2020-06-19
EGAS00001004497
Molecular analysis of CRC in patients with Primary Sclerosing Cholangitis (PSC) and Inflammatory Bowel Disease (IBD)
Cancer Genomics
2020-06-19
EGAS00001004499
Uterine leiomyoma: DNA methylation, chromatin activity and gene expression
Other
2020-06-22
EGAS00001004502
Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes
Transcriptome Analysis
2020-06-22
EGAS00001004503
Peripheral immunoprofiling of stratifies COVID-19 patients based on disease-specific neutrophil signatures
Other
2020-06-22
EGAS00001004504
Human T-bet governs innate and innate-like adaptive IFN-g immunity against mycobacteria.
Other
2020-06-23
EGAS00001004505
RNA-seq data from 121 tumor samples with muscle invasive bladder cancer.
Other
2020-06-24
EGAS00001004507
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Other
2020-06-25
EGAS00001004508
Three-dimensional human alveolar stem cell culture models reveal infection response to SARS-CoV-2
Other
2020-06-25
EGAS00001004510
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Other
2020-06-26
EGAS00001004511
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Other
2020-06-26
EGAS00001004512
A reference map of potential determinants for the human serum metabolome
Other
2020-06-28
EGAS00001004515
EPIC arrays data for chemotherapy response project
Other
2020-06-29
EGAS00001004516
Transcriptomic profiling of lymphedema
Other
2020-06-29
EGAS00001004517
Degradation of Cyclin K/CDK12 is a druggable vulnerability of colorectal cancer (H012)
Cancer Genomics
2020-06-29
EGAS00001004518
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Other
2020-06-30
EGAS00001004519
SNP arrays for chemotherapy response project
Other
2020-06-30
EGAS00001004521
Preoperative ipilimumab plus nivolumab in locoregionally advanced urothelial cancer (NABUCCO Cohorts 1 and 2)
Other
2020-07-01
EGAS00001004523
An epigenetic single-cell atlas of IDH-mutant glioma reveals the role of ATRX in shaping tumor composition
Other
2020-07-01
EGAS00001004524
Changes in alternative splicing and associated neo-antigens due to therapy
Other
2020-07-01
EGAS00001004525
Multiscale heterogeneity in gastric adenocarcinoma evolution is an obstacle to precision medicine
Cancer Genomics
2020-07-01
EGAS00001004527
WES sequencing of malignant peripheral nerve sheath tumours
Other
2020-07-02
EGAS00001004528
RNA seq of MPNST tumour samples
Other
2020-07-02
EGAS00001004532
RNA Sequencing of paediatric patients with B lymphoblastic leukemia
Other
2020-07-06
EGAS00001004533
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Other
2020-07-06
EGAS00001004534
Transcriptomic analysis of the Phase 3 COMPARZ clinical trial
Other
2020-07-06
EGAS00001004535
Whole genome sequencing for novel neuromuscular disease gene discovery
Other
2020-07-07
EGAS00001004536
Multiomic profiling of early-passage melanoma cell lines.
Other
2020-07-07
EGAS00001004538
Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection
Other
2020-07-07
EGAS00001004539
Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib
Other
2020-07-07
EGAS00001004540
Whole Genome Sequencing of 317 individuals from the Pacific region
Other
2020-07-08
EGAS00001004541
Giant congenital nevi exome sequencing
Other
2020-07-09
EGAS00001004542
Gene expression profiling of nasopharyngeal carcinoma
Other
2020-07-09
EGAS00001004544
MGMT genomic rearrangements contribute to chemotherapy resistance in gliomas
Other
2020-07-12
EGAS00001004545
Conserved interferon-gamma signaling and decreased immune exclusion programs in responses to immune checkpoint blockade therapy
Other
2020-07-12
EGAS00001004546
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Other
2020-07-13
EGAS00001004548
A Multifactorial Tumor and Immune Cell Profile Determines Response to Immune Checkpoint blockade in Melanoma
Other
2020-07-13
EGAS00001004550
Therapeutic vulnerabilities in the DNA damage response for the treatment of ATRX mutant neuroblastoma
Other
2020-07-14
EGAS00001004551
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Other
2020-07-14
EGAS00001004552
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Other
2020-07-14
EGAS00001004554
Prospective high-throughput genome profiling in advanced cancers:
Other
2020-07-15
EGAS00001004555
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM67 WES
Other
2020-07-16
EGAS00001004556
Novel mutations in TOP2A in gliomas
Other
2020-07-20
EGAS00001004557
The Genomic Landscape of Prostate Cancer Brain Metastases
Cancer Genomics
2020-07-20
EGAS00001004558
Deep MRD profiling defines outcome and unveils different modes of treatment resistance in standard and high risk myeloma
Cancer Genomics
2020-07-21
EGAS00001004559
Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves
Epigenetics
2020-07-21
EGAS00001004561
Cell types of the human retina and its organoids at single-cell resolution. Cowan et al
Other
2020-07-21
EGAS00001004562
RNASeq of PDX and CDX tumours treated with ADC
Other
2020-07-21
EGAS00001004564
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma
Other
2020-07-22
EGAS00001004567
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM066-WES
Other
2020-07-23
EGAS00001004570
BELOB: Ribo-minus RNA-seq data corresponding to 96x GBM samples from the BELOB trial.
Other
2020-07-23
EGAS00001004571
ScRNA-seq of PBMC and whole blood samples reveals a dysregulated myeloid cell compartment in severe COVID-19
Other
2020-07-24
EGAS00001004572
Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk paediatric cancer
Other
2020-07-24
EGAS00001004574
Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial
Other
2020-07-24
EGAS00001004575
Exome and transcriptome sequencing of Desmoplastic Small Round Cell Sarcoma
Other
2020-07-26
EGAS00001004576
Single cell RNA sequencing of CD19 CAR T-cell infusion products
Other
2020-07-26
EGAS00001004578
Exome sequencing of paired primary tumor and metastatic breast cancer
Other
2020-07-28
EGAS00001004582
TransNEO neoadjuvant breast cancer study
Cancer Genomics
2020-07-29
EGAS00001004583
Hydroxycarbamide effect on DNA methylation and gene expression in MPN patients
Other
2020-07-29
EGAS00001004584
Functional screening on patient-derived organoids identifies a therapeutic bispecific antibody that triggers EGFR degradation in LGR5+ tumor cells
Other
2020-07-29
EGAS00001004585
RNA sequencing of chondrosarcoma
Other
2020-07-29
EGAS00001004586
Cerebral organoid model reveals excessive proliferation of human caudal late interneuron progenitors in Tuberous Sclerosis Complex
Other
2020-07-30
EGAS00001004587
Project MinE Illumina Infinium HumanMethylation450 (450k) BeadChip data on 2,790 Dutch whole blood samples, including 1,761 ALS patients of which 119 are known carriers of the C9orf72 repeat expansion.
Other
2020-07-30
EGAS00001004588
Mutational signatures in head and neck cancer (H019)
Other
2020-07-31
EGAS00001004592
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Other
2020-08-01
EGAS00001004593
Somatic mutations in healthy and leukemic blood progenitors reveal evolutionary mechanisms underlying childhood leukemia and differential patient outcome
Cancer Genomics
2020-08-03
EGAS00001004594
Molecular sub-classification of hormone receptor-positive breast cancer
Other
2020-08-05
EGAS00001004595
Using human induced pluripotent stem cell-derived oligodendrocytes to explore cellular phenotypes associated with t(1;11) translocation.
Other
2020-08-05
EGAS00001004596
A GWAS for cutaneous leishmaniasis in Brazil
Other
2020-08-06
EGAS00001004597
Gene expression profiles of disseminated breast cancer cells
Transcriptome Analysis
2020-08-06
EGAS00001004599
Whole Exome Sequences from Iberian Roma samples
Other
2020-08-06
EGAS00001004600
A Universal Gut Metagenomic-Derived Signature Predicts Cirrhosis
Other
2020-08-06
EGAS00001004601
The endometrial transcription landscape of MRKH syndrome
Other
2020-08-07
EGAS00001004603
Whole Exome Sequencing of High grade T1 non-muscle invasive bladder cancer
Other
2020-08-09
EGAS00001004610
RRBS MDACC Lung PreCancer
Other
2020-08-14
EGAS00001004611
Prime editing for functional repair in patient-derived disease models
Other
2020-08-14
EGAS00001004612
High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune contexture, clinical outcome and sensitivity to targeted therapies
Cancer Genomics
2020-08-14
EGAS00001004613
PCa-LINES
Other
2020-08-17
EGAS00001004614
Patient-tailored design for selective co-inhibition of leukemic cell subpopulations
Other
2020-08-17
EGAS00001004615
Plasma ctDNA is a tumor tissue surrogate and enables clinical-genomic stratification of metastatic bladder cancer
Cancer Genomics
2020-08-17
EGAS00001004619
Queensland Melanoma Genomic Biomarker Study
Other
2020-08-19
EGAS00001004620
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Whole Genome Sequencing
2020-08-20
EGAS00001004621
SureTypeSC - accurate genotyping of single-cell SNP array data
Other
2020-08-20
EGAS00001004623
Single-cell RNA-seq of celiac disease-specific plasma cells
Other
2020-08-20
EGAS00001004624
16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer
Other
2020-08-20
EGAS00001004625
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Population Genomics
2020-08-21
EGAS00001004627
GWAS in bullous pemphigoid in Germans
Other
2020-08-21
EGAS00001004629
Hepatitis B virus integrations promote local and distant oncogenic driver alterations in hepatocarcinogenesis
Other
2020-08-24
EGAS00001004630
Targeted sequencing of breast cancer susceptibility genes for 1,995 Japanese breast cancer patients
Other
2020-08-24
EGAS00001004632
Mutational landscape of eccrine porocarcinoma (sweat gland tumour)
Other
2020-08-24
EGAS00001004633
RNA-seq data of HGG PDOX study
RNASeq
2020-08-24
EGAS00001004636
Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression
Other
2020-08-25
EGAS00001004638
Molecular classification improves risk assessment in adult B-lineage ALL: Patients on the international UKALLXII-ECOG2993 trial.
Other
2020-08-25
EGAS00001004639
Population Genomics of Native Americans from Andes and Amazon
Population Genomics
2020-08-25
EGAS00001004640
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Other
2020-08-26
EGAS00001004641
Characterization of stromal tumor-infiltrating lymphocytes and genomic alterations in metastatic lobular breast cancer
Cancer Genomics
2020-08-26
EGAS00001004642
Genomewide detection of cytosine methylation by single molecule real-time sequencing
Other
2020-08-27
EGAS00001004646
RNA sequencing of follicular T cell lymphoma
Cancer Genomics
2020-08-31
EGAS00001004647
Analysis of transcriptomic profiles from affected and recovered muscle biopsies from children with reversible infantile respiratory chain deficiency.
Other
2020-08-31
EGAS00001004648
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Other
2020-08-31
EGAS00001004649
Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Other
2020-09-01
EGAS00001004650
Genome-wide information of Peruvian Native American
Population Genomics
2020-09-02
EGAS00001004651
Cerebrospinal fluid circulating tumour DNA allows the characterisation and monitoring of medulloblastoma
Other
2020-09-02
EGAS00001004653
Single nucleus and in situ RNA sequencing reveals cell topographies in the human pancreas
Other
2020-09-02
EGAS00001004654
Exome sequencing of DNA from pituitary neuroendocrine tumor (PitNET) and germline DNA from the same patient
Other
2020-09-03
EGAS00001004655
An Integrated Approach to Patient Stratification and Therapy Selection in Acute Myeloid Leukemia
Cancer Genomics
2020-09-04
EGAS00001004656
Single cell RNA-sequencing of GSCs and GBM tumours
Other
2020-09-05
EGAS00001004657
Tissue-specific cell-free DNA degradation quantifies circulating tumor DNA burden
Other
2020-09-08
EGAS00001004659
Molecular and functional profiling of plasmablastic lymphoma
Other
2020-09-09
EGAS00001004660
Aggressive PDACs show hypomethylation of repetitive elements and the execution of an intrinsic IFN program linked to a ductal cell-of-origin
Cancer Genomics
2020-09-09
EGAS00001004661
scRNA-seq of patient-derived PDAC organoids
Other
2020-09-09
EGAS00001004662
Chromothripsis in human breast cancer (HIPO K26K/H017/A017)
Other
2020-09-11
EGAS00001004663
Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia
Other
2020-09-13
EGAS00001004664
Tumour gene expression signature in primary melanoma predicts long-term outcomes: A prospective multicentre study
Other
2020-09-14
EGAS00001004665
Human breast transcriptome analysis
Other
2020-09-14
EGAS00001004666
Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib
Other
2020-09-15
EGAS00001004668
Transcriptomic intra-tumor heterogeneity of colorectal cancer varies depending on tumor location within the colorectum
Other
2020-09-15
EGAS00001004669
Exploration of coding and non-coding variants in cancer using GenomePaint.
Other
2020-09-15
EGAS00001004670
Copy number profiling of circulating cell-free DNA from high grade serous ovarian cancer patients
Cancer Genomics
2020-09-17
EGAS00001004671
TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients.
Other
2020-09-17
EGAS00001004672
mutational landscape of normal human breast
Other
2020-09-17
EGAS00001004673
Genomic profiling of patient-derived xenografts and organoids in prostate cancer
Cancer Genomics
2020-09-17
EGAS00001004674
Foetal_phylogeny_8pcw___WGS_of_LCM_tissues
Other
2020-09-17
EGAS00001004675
Transcriptomic profiling of patient-derived xenografts and organoids in prostate cancer
Transcriptome Analysis
2020-09-18
EGAS00001004677
Organoid_Derivation_Project___GRCh38___RNAseq
Other
2020-09-18
EGAS00001004680
Multifocal ileal NETs study WES
Exome Sequencing
2020-09-21
EGAS00001004681
Multifocal ileal NETs study WGS HFF7VCCXY
Whole Genome Sequencing
2020-09-21
EGAS00001004682
International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia
Other
2020-09-21
EGAS00001004683
Molecular analysis of FIT interval colorectal cancers
Other
2020-09-21
EGAS00001004684
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Other
2020-09-21
EGAS00001004686
Molecular analysis of post-colonoscopy CRC (PCCRC)
Other
2020-09-22
EGAS00001004689
COVID-19 Postmortem Lung snRNA-seq
Other
2020-09-22
EGAS00001004693
UROMOL 2020 - RNA-seq data
Other
2020-09-24
EGAS00001004694
Regulatory T cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors
Other
2020-09-24
EGAS00001004695
Human gastrointestinal epithelia of the esophagus, stomach and duodenum resolved at single-cell resolution
Other
2020-09-25
EGAS00001004696
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (mouse)
Other
2020-09-27
EGAS00001004697
Ultraviolet radiation drives mutations in a subset of mucosal melanomas
Other
2020-09-29
EGAS00001004700
Network-based systems pharmacology identifies heterogeneity in LCK and BCL2 signaling and differential vulnerability of T-cell acute lymphoblastic leukemia to targeted therapy
Other
2020-10-02
EGAS00001004701
Integrative Analysis of Pediatric Acute Leukemia Identifies Acute Myeloid/T-Lymphoblastic Leukemia Subtype that Spans a T Lineage and Myeloid Continuum with Distinct Prognoses
Other
2020-10-02
EGAS00001004702
Chromosomal copy number heterogeneity predicts survival rates across cancers
Other
2020-10-05
EGAS00001004704
A comprehensive characterization of the cell-free transcriptome reveals tissue- and subtype-specific biomarkers for cancer detection
Other
2020-10-06
EGAS00001004705
Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma
Other
2020-10-07
EGAS00001004706
Pancreatic cancer RNA sequencing
Cancer Genomics
2020-10-07
EGAS00001004707
Resident memory CD8 T cell in human lung cancer
RNASeq
2020-10-07
EGAS00001004709
A novel orthotopic patient-derived xenograft model of radiation-induced glioma following medulloblastoma
Other
2020-10-09
EGAS00001004710
Genome-wide somatic variants in CRC (GRCh38)
Whole Genome Sequencing
2020-10-09
EGAS00001004712
Organoid_Derivation_Project___GRCh38___WGS
Other
2020-10-11
EGAS00001004714
Transcriptome Sequencing Data of High Grade Serous Ovarian Cancer
Other
2020-10-12
EGAS00001004717
Single-cell RNA sequencing of bronchoalveolar lavages from COVID-19 patients
Other
2020-10-13
EGAS00001004718
CAR_T_cell_Study
Transcriptome Analysis
2020-10-13
EGAS00001004719
STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma
Other
2020-10-13
EGAS00001004722
HCA_Placental_Infection_Atlas
Other
2020-10-14
EGAS00001004723
HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA
Other
2020-10-14
EGAS00001004724
Multiomics Characterization of Low-grade Serous Ovarian Carcinoma
Other
2020-10-14
EGAS00001004727
HCA_Female_Reproductive_Adult_WSSS_RNA
Transcriptome Analysis
2020-10-14
EGAS00001004728
Microbiota 16S sequencing study in NSCLC patients eligible for surgery without neoadjuvant treatment
Other
2020-10-15
EGAS00001004729
Multi Omics of glioma in the the Chinese Glioma Genome Atlas (CGGA) project
Cancer Genomics
2020-10-15
EGAS00001004733
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Other
2020-10-16
EGAS00001004734
Identification of rare germline variants in familial multiple myeloma
Other
2020-10-16
EGAS00001004735
Multi-region whole-exome sequencing of 10 neuroblastoma cases
Other
2020-10-16
EGAS00001004736
Study of tumor RNA expression differences between treated and untreated PitNET patients
Other
2020-10-16
EGAS00001004739
Prognostic and therapeutic significance of leukemia subtypes and minimal residual disease measurements in pediatric acute lymphoblastic leukemia treated with contemporary risk-directed trial: a cohort study
Other
2020-10-16
EGAS00001004740
Single Cell ATAC-Seq on human cord-blood derived HSPC.
Epigenetics
2020-10-16
EGAS00001004741
ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line
Epigenetics
2020-10-16
EGAS00001004742
Bulk ATAC-Seq on sorted cord blood hematopoietic populations
Epigenetics
2020-10-16
EGAS00001004743
Hi-C on the OCIAML-2 Cell Line
Epigenetics
2020-10-16
EGAS00001004744
Low-C on Human CB-derived LT-HSC and ST-HSC
Epigenetics
2020-10-16
EGAS00001004745
RNA_Seq on Human CB-derived LT-HSC with shCTCF or control vector
RNASeq
2020-10-16
EGAS00001004746
Extramammary Paget Disease
Other
2020-10-19
EGAS00001004748
Small molecule screen reveals synergy of cell cycle checkpoint kinase inhibitors with DNA-damaging chemotherapies in medulloblastoma (RNAseq dataset)
RNASeq
2020-10-19
EGAS00001004749
DIPG RNA and exome sequencing
Other
2020-10-19
EGAS00001004750
The evolution of adult T-cell acute lymphoblastic leukemia
Other
2020-10-19
EGAS00001004751
Characterization of T cell tumor infiltration in brain metastases through the analysis of the cerebrospinal fluid
Cancer Genomics
2020-10-19
EGAS00001004752
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Other
2020-10-19
EGAS00001004753
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Other
2020-10-20
EGAS00001004754
Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma
Other
2020-10-20
EGAS00001004755
Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (microarray)
Other
2020-10-20
EGAS00001004756
Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (WGS)
Whole Genome Sequencing
2020-10-20
EGAS00001004757
Much ado about nothing? - Off-target amplification can lead to false positive bacterial brain microbiome detection in healthy and Parkinson's disease individuals
Other
2020-10-20
EGAS00001004758
The transition from normal lung anatomy to minimal and established fibrosis in Idiopathic Pulmonary Fibrosis
RNASeq
2020-10-21
EGAS00001004760
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing
Other
2020-10-22
EGAS00001004763
Dynamics of genome architecture and chromatin function during human B cell differentiation and neoplastic transformation
Other
2020-10-22
EGAS00001004764
Immunological hallmarks for clinical response to BCG in bladder cancer
Other
2020-10-23
EGAS00001004765
Metabolic requirements of the metastasis-initiating tumour cell population using oral squamous cell carcinoma (OSCC) as a model system
Cancer Genomics
2020-10-26
EGAS00001004766
Epigenome-wide association study of asthma remission in whole blood and nasal epithelium
Epigenetics
2020-10-26
EGAS00001004767
Overactivation of the IGF signalling pathway in osteosarcoma
Other
2020-10-26
EGAS00001004768
RNA-seq of uncultured CD112high and CD112low long-term(LT) human hematopoietic stem cells (HSC) and cultured and lentiviral transduced (CTRL, INKA1-OE) LT- and short-term HSC from umbilical cord blood
Other
2020-10-26
EGAS00001004769
Single cell RNA-sequencing (scRNA-seq) of the human hematopoietic stem cell compartment (CD34+CD38-CD45RA-)
Other
2020-10-26
EGAS00001004770
Transcriptomic profiling of prostate cancer metastasis xenograft models reveals conservation of bone microenvironment signatures
Transcriptome Analysis
2020-10-29
EGAS00001004772
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19
Other
2020-10-29
EGAS00001004773
Colorectal cancer cells possess an equipotent capacity to enter a developmental pausing-like state to survive chemotherapy
Cancer Genomics
2020-10-29
EGAS00001004777
Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Whole Genome Sequencing
2020-11-02
EGAS00001004780
Cell of Origin and Early Evolution of Leukemia in Down Syndrome
Other
2020-11-02
EGAS00001004781
Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines)
Other
2020-11-03
EGAS00001004782
Gene expression from human iPSC derived cortical neurons
Other
2020-11-03
EGAS00001004783
Rna-Seq Leiomyosarcoma subtypes
Other
2020-11-04
EGAS00001004784
Mechanisms of active DNA demethylation in human monocytes
Epigenetics
2020-11-04
EGAS00001004786
Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Other
2020-11-06
EGAS00001004788
Methylation analysis for plasma DNA of patients with organ transplantation
Other
2020-11-09
EGAS00001004789
MutationalPatterns2: The one stop shop for the analysis of mutational processes: DNA repair deletions
Whole Genome Sequencing
2020-11-09
EGAS00001004791
Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Other
2020-11-11
EGAS00001004792
RNA-seq study of a Princess Margaret Cancer Centre human acute myeloid leukemia patient cohort
Other
2020-11-11
EGAS00001004793
Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia
Other
2020-11-12
EGAS00001004794
RNAseq cutaneous and uveal melanoma liver metastases
Other
2020-11-12
EGAS00001004795
WES cutaneous and uveal melanoma liver metastases
Other
2020-11-12
EGAS00001004796
Neuroblastoma Cell Line Circle-seq
Other
2020-11-12
EGAS00001004797
Primary Neuroblastoma Circle-seq
Other
2020-11-12
EGAS00001004798
RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3
Other
2020-11-12
EGAS00001004800
BRCA2, ATM, and CDK12 defects differentially shape prostate tumor driver genomics and clinical aggression
Cancer Genomics
2020-11-13
EGAS00001004805
Single cell RNA sequencing of relapsed/refractory multiple myeloma
Other
2020-11-13
EGAS00001004808
CTCF-dependent enhancer hijacking by the EVI1 oncogene in leukemia
Other
2020-11-13
EGAS00001004809
BIOKEY: A single-cell catalogue of the dynamic changes underlying Checkpoint Immunotherapy response in Early Breast Cancer
Other
2020-11-15
EGAS00001004810
BCL11B enhancer hijacking defines a subtype of lineage ambiguous stem cell leukemia
Other
2020-11-15
EGAS00001004812
Integrative multi-omic analyses of malignant pleural mesothelioma
Other
2020-11-16
EGAS00001004813
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Other
2020-11-16
EGAS00001004814
Transcriptional profiling of ovarian tumours and cell lines
Other
2020-11-16
EGAS00001004816
DNA polymerase and mismatch repair deficient cancers exert distinct genome-wide microsatellite signatures 2
Whole Genome Sequencing
2020-11-16
EGAS00001004819
Long-read and short-read isoform sequencing in breast cancer
Other
2020-11-17
EGAS00001004820
Gut metagenomic data of 2,338 Pinggu adults
Other
2020-11-18
EGAS00001004821
Integrated Genomic and Transcriptomic Analysis Reveals Unique Characteristics of Hepatic Metastases and Pro-metastatic Role of Complement C1q in Pancreatic Ductal Adenocarcinoma
Cancer Genomics
2020-11-18
EGAS00001004824
Reconstruction of human phylogenetic trees using single-cell genome sequencing
Other
2020-11-19
EGAS00001004825
Molecular response of AML blasts to Aza-treatment.
Other
2020-11-20
EGAS00001004826
The genetic structure of Norway
Other
2020-11-20
EGAS00001004827
Volasertib preclinical activity in high-risk hepatoblastoma
Other
2020-11-20
EGAS00001004828
Alveolar Rhabdomyosarcoma case report
Other
2020-11-20
EGAS00001004829
scRNA-seq of HGSC tumor and ascites
Other
2020-11-23
EGAS00001004830
MicroRNAs signatures from CSF extracellular vesicles of Parkinson’s Disease patients
RNASeq
2020-11-23
EGAS00001004832
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – Whole exome sequencing
Other
2020-11-24
EGAS00001004833
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – RNA sequencing
Other
2020-11-24
EGAS00001004835
Differential gene expression in the colon mucosa of irritable bowel syndrome patients with mixed type symptoms
Other
2020-11-24
EGAS00001004836
Effect_of_FAM50_knockout_on_the_transcriptome
Cancer Genomics
2020-11-24
EGAS00001004837
Inherited CD28 deficiency in otherwise healthy patients with disseminated warts and giant horns
Transcriptome Analysis
2020-11-24
EGAS00001004838
WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants
Whole Genome Sequencing
2020-11-24
EGAS00001004839
An essential role for MYB in driving oncogenic EVI1 expression in enhancer-rearranged leukemias
Other
2020-11-25
EGAS00001004841
Molecular profiling of an AML case following treatment with a BCL2 inhibitor
Other
2020-11-26
EGAS00001004843
Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma
Other
2020-11-27
EGAS00001004844
Single Cell MK and HSC sequencing
Other
2020-11-27
EGAS00001004847
Circulating Tumor DNA in Checkpoint Inhibitor treated Lung Cancer
Other
2020-11-30
EGAS00001004850
The Acquisition of Molecular Drivers in Pediatric Therapy-Related Myeloid Neoplasms
Other
2020-11-30
EGAS00001004851
AGECAN - Interespecies conservation of brain specific DNA methylation in aging and cancer
Epigenetics
2020-11-30
EGAS00001004852
Tumor HTG EdgeSeq from metastatic castrate resistant prostate cancer
Other
2020-12-01
EGAS00001004856
Shwachman-Diamond syndrome sequencing study
Other
2020-12-01
EGAS00001004857
Comprehensive genomic and transcriptomic analysis of three synchronous primary tumours and a recurrence from a head and neck cancer patient
Other
2020-12-01
EGAS00001004860
PBMC gene expression profiles in diet treated celiac disease upon oral gluten challenge
Transcriptome Analysis
2020-12-01
EGAS00001004861
Bulk-RNA Sequencing of high-grade pancreatic and non-pancreatic Neuroendocrine Neoplasms
Other
2020-12-02
EGAS00001004862
UROMOL 2020 - SNP data
Other
2020-12-02
EGAS00001004863
DEREGULATION OF PRE-mRNA SPLICING IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER
Cancer Genomics
2020-12-02
EGAS00001004864
Genomic analysis of a hypermutated gliosarcoma
Other
2020-12-02
EGAS00001004867
Targeted de-methylation of the FOXP3-TSDR
Other
2020-12-03
EGAS00001004868
Genetic makeup of agnospheres
Other
2020-12-03
EGAS00001004869
POPCOL: population-based colonoscopy.
Other
2020-12-03
EGAS00001004870
NIHR BioResource Common Disease Patients 2016
Other
2020-12-03
EGAS00001004871
Single-cell multi-omic profiling of glioblastoma-associated myeloid cells
Transcriptome Analysis
2020-12-03
EGAS00001004872
Biological and Therapeutic Implications of a Unique Subtype of NPM1 Mutated AML
Cancer Genomics
2020-12-03
EGAS00001004877
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Other
2020-12-07
EGAS00001004878
Pancreatic, Small-intestinal and Pulmonary Neuroendocrine Tumors
Other
2020-12-08
EGAS00001004879
Targeted Sequencing of Shwachman-Diamond syndrome bone marrow samples
Other
2020-12-08
EGAS00001004880
Whole Exome sequencing data from Shwachman-Diamond syndrome bone marrow samples
Exome Sequencing
2020-12-08
EGAS00001004881
Single cell sequencing data from Shwachman-Diamond syndrome bone marrow
Other
2020-12-08
EGAS00001004882
Somatic_evolution_in_the_psoriatic_skin
Other
2020-12-09
EGAS00001004884
Molecular evolution and clinical trajectories of prostate cancer identifies novel markers for risk stratification - additional data
Cancer Genomics
2020-12-09
EGAS00001004885
Gut microbiome sequencing in patients receiving combination immune checkpoint blockade
Other
2020-12-10
EGAS00001004886
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Other
2020-12-10
EGAS00001004887
EAC Genomic data
Cancer Genomics
2020-12-10
EGAS00001004888
Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities
Other
2020-12-10
EGAS00001004889
Multi-omics profiling of PSCCE
Other
2020-12-11
EGAS00001004890
Impact of BRCA mutation type in non-tumorous breast tissue transcriptome
Other
2020-12-11
EGAS00001004892
Targeted sequencing DDR genes in cancer stem cells
Other
2020-12-11
EGAS00001004894
Single cell T cell Landscape and T Cell Receptor Repertoire Profiling of AML in Context of PD-1 Blockade Therapy
Other
2020-12-11
EGAS00001004895
Risk and modifying factors in Frontotemporal Dementia
Other
2020-12-12
EGAS00001004897
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (Human)
Other
2020-12-13
EGAS00001004899
Personalised therapy with MEK inhibition leads to a sustained complete response in an adolescent patient with a recurrent malignant peripheral nerve sheath tumor
Other
2020-12-14
EGAS00001004900
Single-cell chromatin accessibility landscape identifies tissue repair program in human regulatory T cells
Other
2020-12-14
EGAS00001004902
Whole genome sequencing of germline DNA from 8 patients with adult granulosa cell tumors (from blood or saliva)
Other
2020-12-14
EGAS00001004903
Finding structural variation and functional consequences from the primary leukemia cells (AML) at the single-cell level
Other
2020-12-14
EGAS00001004904
Oncolytic virotherapy mediated anti-tumor response in primary cutaneous B-cell lymphoma: a single-cell perspective
RNASeq
2020-12-14
EGAS00001004905
Dual targeting of polyamine synthesis and uptake in diffuse intrinsic pontine gliomas
Other
2020-12-15
EGAS00001004906
Mutational Landscape of Plasmablastic Lymphoma
Other
2020-12-15
EGAS00001004907
Blood RNA-seq from Mexican DMD patients and healthy controls
Other
2020-12-15
EGAS00001004908
Mutations in SKI in Shprintzen-Goldberg syndrome lead to attenuated TGFB responses through SKI stabilization
RNASeq
2020-12-15
EGAS00001004909
Single cell multi-omic data of glioblastoma evolution under therapy
Other
2020-12-16
EGAS00001004912
Neutrophils infected with Leishmania donovani
Other
2020-12-17
EGAS00001004913
ChIP-seq of plasma cell-free nucleosomes identifies gene expression programs of the cells-of-origin
Other
2020-12-17
EGAS00001004915
Selective Elimination of Immunosuppressive T cells in Patients with Multiple Myeloma
Cancer Genomics
2020-12-17
EGAS00001004918
Oxford Nanopore RNA sequencing for HLA typing
Other
2020-12-18
EGAS00001004925
Finding structural variation and functional consequences from the primary leukemia cells (CLL) at the single-cell level
Other
2020-12-20
EGAS00001004926
Mutational consequences of hematopoietic stem cell transplantation in humans
Whole Genome Sequencing
2020-12-21
EGAS00001004927
Short and long-read sequencing of Brugada syndrome samples
Other
2020-12-21
EGAS00001004928
Single-cell RNA-seq of bronchoalveolar lavage (BAL) fluid in severe COVID-19 and SARS-CoV-2 stimulated classical blood monocytes
Other
2020-12-23
EGAS00001004929
Whole genome sequencing delineates regulatory, structural, and cryptic splice variants in early onset cardiomyopathy
Other
2020-12-23
EGAS00001004930
Phase Ib of olaparib and capivasertib
Other
2020-12-25
EGAS00001004931
Illumina RNA sequencing for HLA expression qauntification
Other
2020-12-28
EGAS00001004933
The Genetic History of Greenlandic-European contact
Other
2020-12-31
EGAS00001004934
Detection of Gene Fusions using Targeted Next-Generation Sequencing – a Comparative Evaluation
Cancer Genomics
2021-01-04
EGAS00001004935
Single Cell Dissection of the Tumour Microenvironment Reveals Dynamic Interplay Shaping the Tumour Immunity Continuum in Ovarian Cancer
Other
2021-01-05
EGAS00001004936
Single-cell analysis of the multicellular ecosystem in viral carcinogenesis by HTLV-1
Other
2021-01-05
EGAS00001004939
Tissue and plasma RNA from esophageal cancer and precursor lesions
Other
2021-01-06
EGAS00001004940
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Other
2021-01-06
EGAS00001004941
Genomic insights into the pathogenesis of Epstein-Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon-based sequencing
Other
2021-01-06
EGAS00001004942
Multi-institutional collaboration to characterize 5hmC in prostate cancer, both tumor biopsies and cfDNA.
Other
2021-01-06
EGAS00001004943
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Other
2021-01-06
EGAS00001004944
Fasting-mimicking diet reshapes antitumor immunity in cancer patients
RNASeq
2021-01-07
EGAS00001004946
Endothelium-derived stromal cells contribute to bone marrow niche formation
Other
2021-01-09
EGAS00001004947
Genetic insights into the biological mechanisms governing human ovarian ageing
Other
2021-01-11
EGAS00001004948
BCR Signaling in human BM PC
Other
2021-01-11
EGAS00001004949
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Other
2021-01-11
EGAS00001004950
CASCADE metastatic melanoma study
Other
2021-01-12
EGAS00001004951
Upper respiratory microbiome of COVID-19 patients
Other
2021-01-12
EGAS00001004953
The temporal mutational and immune tumour microenvironment remodelling of HER2-negative primary breast cancers
Other
2021-01-13
EGAS00001004959
GCP study
Cancer Genomics
2021-01-14
EGAS00001004960
Sequencing of cell-free DNA from breast cancer patients
Other
2021-01-15
EGAS00001004961
Copy number and mutation profiling of Stage 1 epithelial ovarian cancer biopsies
Other
2021-01-15
EGAS00001004962
Cell-free DNA TAPS for early cancer detection
Other
2021-01-15
EGAS00001004963
Assessment of cannabidiol and Δ9-tetrahydrocannabiol in mouse models of medulloblastoma
Other
2021-01-16
EGAS00001004964
Preliminary Results from the Initiative for Molecular Profiling and Advanced Cancer Therapy 2 (IMPACT 2) Study
Cancer Genomics
2021-01-18
EGAS00001004965
Evaluation of capture and amplicon-based targeted sequencing methods on formalin-fixed tumours
Other
2021-01-18
EGAS00001004966
Multiomics analyses of Parkinson's disease midbrains
Other
2021-01-18
EGAS00001004967
Transcriptomic analysis of TFEB knockdown in LT-HSC.
Other
2021-01-18
EGAS00001004968
Transcriptomic analysis of human hematopoietic populations sorted from umbilical cord blood.
Other
2021-01-18
EGAS00001004969
Transcriptomic analysis of TFEB overexpression in LT-HSC, ST-HSC and MEP
Other
2021-01-18
EGAS00001004970
Transcriptomic analysis of MYC overexpression in LT-HSC.
Other
2021-01-18
EGAS00001004971
Chromatin accessibility analysis of TFEB overexpression in LT-HSC
Other
2021-01-18
EGAS00001004973
Application of short-RNA-seq in post-mortem human hippocampi from the Calgary Brain Bank (CBB) to assess transcriptome-wide deregulation in processing of SINE Alu RNAs in Alzheimer’s disease
Other
2021-01-19
EGAS00001004974
Macrophage response in preterm infants compared to term infants
Other
2021-01-19
EGAS00001004975
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Cancer Genomics
2021-01-19
EGAS00001004979
SNParray
Other
2021-01-21
EGAS00001004982
Integrative Molecular Classification of Meningiomas
Other
2021-01-21
EGAS00001004987
High-grade serous ovarian cancer refined with single-cell RNA-sequencing
Other
2021-01-24
EGAS00001004988
RNA-sequencing of gluten-reactive and non-reactive T-cells from blood samples of treated CeD patients during a gluten-challenge
Other
2021-01-24
EGAS00001004989
Single-cell T-cell receptor sequencing of intraepithelial CD8+ αβ T-cells in celiac disease
Other
2021-01-24
EGAS00001004990
Evolutionary dynamics of neuroblastoma
Other
2021-01-25
EGAS00001004992
Targeting the Epichaperome As an Effective Precision Medicine Approach in a Novel PML-SYK Fusion Acute Myeloid Leukemia
Transcriptome Analysis
2021-01-26
EGAS00001004994
Somatic mutations in lymphocytes in patients with immune-mediated aplastic anemia
Transcriptome Analysis
2021-01-27
EGAS00001004995
Peruvian Genome Project - Whole Genome Sequencing
Other
2021-01-27
EGAS00001004996
Boson HCV infected liver bulk RNASeq study
Other
2021-01-27
EGAS00001004997
Clinical outcomes in ctDNA-positive urothelial carcinoma patients treated with adjuvant immunotherapy
Other
2021-01-27
EGAS00001004998
The genomic landscape of childhood acute lymphoblastic leukaemia with intrachromosomal amplification of chromosome 21 (iAMP21-ALL)
Other
2021-01-28
EGAS00001004999
Whole genome sequencing of patients affected by acute intermittent porphyria
Other
2021-01-28
EGAS00001005000
single cell sequencing of resting and Influenza-stimulated mononcluear phagocytes of African and Europeans with varying degree of ex-vivo susceptibility to Influenza
Other
2021-01-28
EGAS00001005001
Relapse series of two Pediatric ALL patients
Other
2021-01-29
EGAS00001005004
Fibromyalgia versus small fiber neuropathy: Diverse keratinocyte transcriptome signature
Other
2021-01-29
EGAS00001005005
Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas
Other
2021-01-30
EGAS00001005006
Longitudinal single-cell RNA-seq data of metastatic ovarian cancer
Transcriptome Analysis
2021-01-30
EGAS00001005008
Mutations in the RAS/MAPK pathway drive replication repair deficient hypermutated tumors and confer sensitivity to MEK inhibition
Other
2021-01-30
EGAS00001005009
DO NOT USE - Whole genome sequencing of SI-NETs from six patients
Other
2021-01-31
EGAS00001005010
Longitudinal single-cell RNA-seq data of metastatic ovarian cancer
Other
2021-01-31
EGAS00001005012
MBD4 targeted sequencing
Other
2021-02-01
EGAS00001005013
Intratumoral plasma cells predict outcomes to PD-L1 blockade in non-small cell lung cancer
Other
2021-02-01
EGAS00001005014
Primary prostate Hi-C
Other
2021-02-01
EGAS00001005015
RNA sequencing of PTCL-NOS
Cancer Genomics
2021-02-02
EGAS00001005018
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Other
2021-02-02
EGAS00001005019
Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma
Other
2021-02-02
EGAS00001005020
Gut metagenome/FINRISK 2002 (Salosensaari et al. Nature Comms 2021)
Other
2021-02-02
EGAS00001005021
Single cell RNAseq of lung adenocarcinoma
Other
2021-02-03
EGAS00001005022
Deep genetic affinity between coastal Pacific and Amazonian natives evidenced by Australasian ancestry
Other
2021-02-03
EGAS00001005023
Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma
Other
2021-02-03
EGAS00001005024
Proteotranscriptomic classification and characterization of pancreatic neuroendocrine neoplasms
Other
2021-02-03
EGAS00001005025
Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Other
2021-02-04
EGAS00001005026
Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Other
2021-02-04
EGAS00001005027
The Dutch Microbiome Project: Defining the (un)healthy gut microbiome
Other
2021-02-05
EGAS00001005029
Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Other
2021-02-08
EGAS00001005030
MicroRNA profiling by next-generation sequencing for colorectal cancer screening
Other
2021-02-08
EGAS00001005032
Genomic Study of Gastric Cancer
Other
2021-02-09
EGAS00001005033
The WID-EC test for the detection and risk prediction of endometrial cancer
Epigenetics
2021-02-09
EGAS00001005034
Genome-wide characterization of Kuwaiti Arab Population
Other
2021-02-09
EGAS00001005038
Gut metagenome/FR 2002
Other
2021-02-11
EGAS00001005039
SINGLE-CELL RNA SEQUENCING Single-cell RNA sequencing was performed on 13 ‘mild-moderate’ and 10 ‘critical’ COVID19 PBMC samples
Other
2021-02-11
EGAS00001005040
A rare CTSC mutation in Papillon-Lefèvre Syndrome
Other
2021-02-11
EGAS00001005041
Transcriptome analysis of PBMCs from patients with STAT1 activating mutation
RNASeq
2021-02-11
EGAS00001005042
Test Study for EGA using data from 1000 Genomes Project - Phase 3
Whole Genome Sequencing
2021-02-11
EGAS00001005043
hereditary BrEAst Case CONtrol study
Other
2021-02-11
EGAS00001005044
Single-cell roadmap of immune cell responses in chronic myeloid leukemia
Other
2021-02-11
EGAS00001005045
The DNA methylome of cervical cells and risk of ovarian cancer
Epigenetics
2021-02-12
EGAS00001005046
Using de novo assembly to identify structural variation of complex immune system gene regions
Other
2021-02-12
EGAS00001005047
Single-cell TCR sequencing of gluten-specific T cells from 20 celiac disease patients uploaded on 2021
Other
2021-02-12
EGAS00001005048
Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands
Other
2021-02-12
EGAS00001005049
Combining dasatinib and IFN-α in CML – immunomodulatory effects linked to treatment response and adverse events
Other
2021-02-13
EGAS00001005050
UROMOL 2020 - RNA-seq data for validation
Other
2021-02-15
EGAS00001005051
Bone marrow derived stromal cells from Myelodysplastic Syndromes
Other
2021-02-15
EGAS00001005052
Whole-genome sequencing of a census-based elderly cohort of Brazilians
Whole Genome Sequencing
2021-02-15
EGAS00001005053
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit
Other
2021-02-15
EGAS00001005054
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Other
2021-02-15
EGAS00001005055
The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples
Other
2021-02-16
EGAS00001005057
Characterization of DLBCL with a PMBL gene expression signature
Other
2021-02-17
EGAS00001005060
SARS-CoV-2 escapes CD8 T cell surveillance via mutations in MHC-I restricted epitopes [10x]
Other
2021-02-18
EGAS00001005061
Stromal cell diversity associated with immune evasion in human triple‐negative breast cancer
RNASeq
2021-02-18
EGAS00001005064
Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor.
Other
2021-02-19
EGAS00001005065
Genomic Landscape of Malignant Peripheral Nerve Sheath Tumor-like Melanoma
Other
2021-02-19
EGAS00001005066
Single-cell RNA-seq data from metastatic ovarian cancer for quality control study
Other
2021-02-22
EGAS00001005068
Discovery of cancer prognostic markers based on comparison of gene expression in colorectal cancer samples.
Other
2021-02-22
EGAS00001005069
Sensitive and reproducible cell-free methylome quantification with synthetic spike-in controls
Epigenetics
2021-02-22
EGAS00001005070
Breast tissue methylation analysis
Epigenetics
2021-02-22
EGAS00001005071
Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
Other
2021-02-23
EGAS00001005073
Whole-exome sequencing of hepatocellular carcinoma biopsies (proteogenomic study)
Other
2021-02-23
EGAS00001005074
Transcriptome sequencing of hepatocellular carcinoma biopsies (proteogenomic study)
Other
2021-02-23
EGAS00001005075
Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia
Other
2021-02-24
EGAS00001005076
Liverpool Preterm Birth Biomarker Study
Other
2021-02-25
EGAS00001005077
Anal SCC cell line and parent tumour comparative whole exome sequencing
Other
2021-02-26
EGAS00001005078
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+)
Other
2021-02-26
EGAS00001005081
Molecular analysis of inflammatory myofibroblastic tumor (WGS and WES)
Cancer Genomics
2021-03-01
EGAS00001005083
Multiple migrations to the Philippines during the last 50,000 years
Other
2021-03-01
EGAS00001005084
Clinical significance of novel subtypes of acute lymphoblastic leukemia in the context of minimal residual disease-directed therapy
Other
2021-03-01
EGAS00001005085
Profiling of H3K27ac landscape in immune cells from rheumatoid arthritis patients and healthy controls
Other
2021-03-02
EGAS00001005086
ARAF Mutations Confer Resistance to RAF Dimer Inhibitor Belvarafenib in NRAS- and BRAF- Mutant Melanoma
Other
2021-03-02
EGAS00001005087
Whole exome sequencing from small cell lung cancer patients
Exome Sequencing
2021-03-02
EGAS00001005090
A_cell_atlas_of_the_human_fetal_spine_SB_HDBR_Project_200532
Transcriptome Analysis
2021-03-04
EGAS00001005091
Enrichment of homologous recombination repair alteration in prostate cancer brain metastases
Other
2021-03-04
EGAS00001005093
single-stranded DNA study
Other
2021-03-04
EGAS00001005095
The_evolution_of_CML
Other
2021-03-04
EGAS00001005096
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Other
2021-03-04
EGAS00001005097
Oncogenic cooperation between the TCF7-SPI1 fusion and NRAS(G12D) requires β-catenin activity to drive T-cell acute lymphoblastic leukemia.
Other
2021-03-05
EGAS00001005098
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq
Other
2021-03-05
EGAS00001005102
CRISPR transduction of iPS cells
Other
2021-03-08
EGAS00001005104
Genetic landscape of inherited retinal dystrophies affected cases in Spain
Other
2021-03-09
EGAS00001005106
Comparative transcriptome of CD34+ hematopoietic progenitors from myeloproliferative patients and control donors
Other
2021-03-09
EGAS00001005107
Chronic myelomonocytic leukemia
Other
2021-03-10
EGAS00001005108
Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Other
2021-03-10
EGAS00001005109
Sequencing of cancer autopsies and ctDNA
Other
2021-03-10
EGAS00001005110
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Other
2021-03-10
EGAS00001005111
IG-MYC rearrangement defines a high-risk subgroup of B-cell precursor acute lymphoblastic leukaemia
Cancer Genomics
2021-03-11
EGAS00001005112
The INFORM Precision Medicine Study for High-Risk Pediatric Malignancies
Cancer Genomics
2021-03-11
EGAS00001005115
Cryopreservation of human cancers conserves tumour heterogeneity for single-cell multi-omics analysis
Transcriptome Analysis
2021-03-12
EGAS00001005116
WES of clonally related neuroblastoma and teratoma
Other
2021-03-13
EGAS00001005117
Whole-exome sequencing performed on a patient with chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia
Other
2021-03-14
EGAS00001005118
Identification of novel colorectal cancer predisposition genes
Cancer Genomics
2021-03-15
EGAS00001005121
ATAC-seq of uncultured CD112high and CD112low long-term(LT) human hematopoietic stem cells (HSC) from umbilical cord blood
Other
2021-03-15
EGAS00001005125
Copy number analysis by SNP array
Other
2021-03-16
EGAS00001005127
Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Other
2021-03-17
EGAS00001005128
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Other
2021-03-17
EGAS00001005130
RNA-Seq of vocal fold fibroblasts in Reinke’s edema and control subjects
Other
2021-03-17
EGAS00001005132
Epigenomic profiling and transcriptomic profiling of LUAD patients tumor tissues and tumor adjacent tissues
Other
2021-03-18
EGAS00001005134
Engineering large chromosomal deletions by CRISPR-Cas9
Other
2021-03-19
EGAS00001005137
Characterization of human iPSC-derived dopaminergic neurons with 16p11.2 CNVs
Transcriptome Analysis
2021-03-22
EGAS00001005138
Increased trunk fat is associated with altered gene expression in breast tissue of normal weight women
Transcriptome Analysis
2021-03-22
EGAS00001005140
Mixed Histology Lung Cancers Driven by Transcriptomic Features rather than Genomic Characteristics
Cancer Genomics
2021-03-22
EGAS00001005141
Chemotherapy accelerates genomic aging of normal blood in children treated for cancer
Other
2021-03-23
EGAS00001005144
Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis
Other
2021-03-24
EGAS00001005145
H021-Master Umbrella study2 (not to be released)
Cancer Genomics
2021-03-24
EGAS00001005147
Assessment of the Toll-like receptor 3 response in hepatocytes
Other
2021-03-25
EGAS00001005151
Single-cell transcriptome of human fetal pancreas and in vitro pancreatic spheroids
Other
2021-03-25
EGAS00001005159
WGS bam
Other
2021-03-28
EGAS00001005160
WES bam
Other
2021-03-28
EGAS00001005161
RNA-seq bam
Other
2021-03-28
EGAS00001005171
Genotype data from 'Evidence of the interplay of genetics and culture in Ethiopia'
Other
2021-03-30
EGAS00001005173
An integrated multi-omic cellular atlas of human breast cancers
RNASeq
2021-03-31
EGAS00001005174
sn-RNAseq profiling of the impact of a cytokine storm model in human cardiac organoids
Other
2021-04-01
EGAS00001005178
Single-cell analysis of retinoblastoma heterogeneity
RNASeq
2021-04-01
EGAS00001005180
Degradation of Janus kinases in CRLF2-rearranged acute lymphoblastic leukemia
Other
2021-04-02
EGAS00001005181
G3BP2-KIT drives leukemia amenable to kinase inhibition in Ph-like ALL
Other
2021-04-02
EGAS00001005182
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Other
2021-04-06
EGAS00001005187
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Other
2021-04-07
EGAS00001005188
Platelet response in aspirin adherent pregnant women
Other
2021-04-07
EGAS00001005189
Nasal DNA methylation at three CpG sites predicts childhood allergic disease
Epigenetics
2021-04-07
EGAS00001005194
Single cell and plasma RNA sequencing
Other
2021-04-09
EGAS00001005196
Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients.
Other
2021-04-12
EGAS00001005197
arrayCGH for copy number profiling on tumor DNA from pediatric cancer tissue samples
Other
2021-04-12
EGAS00001005198
sWGS on cfDNA and matching tumor DNA in pediatric cancer
Other
2021-04-12
EGAS00001005199
Paired exome and low-coverage genome sequencing of osteosarcoma
Other
2021-04-12
EGAS00001005201
The T cell receptor repertoire of tumor infiltrating T cells is predictive and prognostic for cancer survival
Other
2021-04-12
EGAS00001005202
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Other
2021-04-12
EGAS00001005203
The distinct DNA methylome of acute lymphoblastic leukemia
Other
2021-04-14
EGAS00001005204
Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma
Other
2021-04-15
EGAS00001005205
Whole-Exome Sequences from Imazighen and non-Imazghen from Tunisia
Other
2021-04-15
EGAS00001005206
High titers and low fucosylation of early phase anti-SARS-CoV-2 IgG promote hyper-inflammation by alveolar macrophages
Other
2021-04-15
EGAS00001005214
Sclerosing epithelioid fibrosarcoma case report
Other
2021-04-15
EGAS00001005215
Sclerosing epithelioid fibrosarcoma case report
Other
2021-04-15
EGAS00001005220
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Other
2021-04-16
EGAS00001005221
Molecular characterization of Barrett’s esophagus at single cell resolution
Other
2021-04-16
EGAS00001005222
Molecular characterization of hepatocellular carcinoma in patients with non-alcoholic steatohepatitis
Other
2021-04-16
EGAS00001005224
Esophageal Adenocarcinoma Organoid Genomics
Other
2021-04-16
EGAS00001005225
Gluten-free microbiome study UMCG
Metagenomics
2021-04-18
EGAS00001005226
Splicing patterns in SF3B1 mutated uveal melanoma generate shared immunogenic tumor-specific neo-epitopes
Other
2021-04-19
EGAS00001005227
Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Other
2021-04-20
EGAS00001005228
Circulating tumor cells Exome sequencing from breast cancer
Other
2021-04-21
EGAS00001005229
Improved Sezary cell detection and novel insights into immunophenotypic and molecular heterogeneity in Sézary syndrome
Other
2021-04-22
EGAS00001005230
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Other
2021-04-22
EGAS00001005232
Male-biased migration from East Africa introduced pastoralism into southern Africa
Population Genomics
2021-04-23
EGAS00001005234
The evolution of hematopoietic cells under cancer therapy
Other
2021-04-25
EGAS00001005235
Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Other
2021-04-25
EGAS00001005237
Whole-genome landscape of adult T-cell leukemia/lymphoma
Other
2021-04-26
EGAS00001005238
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Other
2021-04-26
EGAS00001005241
Single cell sequencing reveals expanded cytotoxic CD4+ T cells and two clusters of peripheral helper T cells in synovial fluid of ACPA+ RA patients
RNASeq
2021-04-26
EGAS00001005242
Evolutionary trajectories and clonal migration underlying tumor progression and lymph node metastasis in resectable lung cancer
Cancer Genomics
2021-04-27
EGAS00001005243
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Other
2021-04-27
EGAS00001005244
The_Little_Princess_Knowledge_Bank_RNAseq
Other
2021-04-27
EGAS00001005245
Host genetic determinants of HIV infection
Other
2021-04-27
EGAS00001005248
Genomic characterization of retinoblastoma
Cancer Genomics
2021-04-27
EGAS00001005250
The genomic landscape of pediatric acute lymphoblastic leukemia
Other
2021-04-29
EGAS00001005253
Combining a Universal Telomerase Based Cancer Vaccine with Ipilimumab in Patients with Metastatic Melanoma - Five-year Follow up of a Phase I/IIa Trial
Other
2021-05-03
EGAS00001005254
Identification and functional characterisation of a rare MTTP variant underlying familial non-alcoholic fatty liver disease
Other
2021-05-03
EGAS00001005255
Comparison of capture-based method for transcriptome profiling of formalin-fixed paraffin embedded tumor samples
Other
2021-05-03
EGAS00001005256
Whole genome sequencing of adult glioblastoma nuclei
Other
2021-05-03
EGAS00001005257
Single-cell RNA sequencing of 6 follicular lymphoma tumors
Other
2021-05-04
EGAS00001005258
CD27hiCD38hi plasmablasts are activated B cells of mixed origin with distinct function
Other
2021-05-04
EGAS00001005263
The Extracellular RNA Quality Control (exRNAQC) study (phase 1)
RNASeq
2021-05-05
EGAS00001005268
Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans
Other
2021-05-05
EGAS00001005270
Molecular characteristics in Burkitt lymphoma over age groups
Other
2021-05-06
EGAS00001005271
Human Inflammatory Skin Disease scRNA-seq
RNASeq
2021-05-06
EGAS00001005273
Exome_sequencing_of_UK_Birth_Cohorts___Avon_Longitudinal_Study_of_Parents_and_Children
Other
2021-05-07
EGAS00001005274
Prediction of HLA genotypes using NGS data
Other
2021-05-07
EGAS00001005276
Genomic and Transcriptomic Profile of Paired Primary-Metastasis Colorectal Tumors
Other
2021-05-07
EGAS00001005277
Extracellular transcriptome in seminal plasma for non-invasive prostate cancer diagnosis
Other
2021-05-10
EGAS00001005280
Impaired Humoral and Cellular Immunity after SARS-CoV2 BNT162b2 (Tozinameran) Prime-Boost Vaccination in Kidney Transplant Recipients
RNASeq
2021-05-10
EGAS00001005281
ATAC-seq data in normal colon mucosa
Other
2021-05-11
EGAS00001005286
Hypoxia acts as an environmental cue for the human TRM differentiation program
Other
2021-05-11
EGAS00001005295
atrial appendage RNA-seq in non-, paroxysmal and persistent atrial fibrillation
Other
2021-05-12
EGAS00001005297
Single-cell profiling of the leukemic and non-leukemic immune cell compartments in CD8+ T-cell Large Granular Lymphocytic Leukemia
Other
2021-05-12
EGAS00001005298
HSC_colony_many_years_post_allogeneic_bone_marrow_transplant_TGS
Other
2021-05-12
EGAS00001005299
ALLoreactive T-Cell receptOr RePertoire in kidnEy tranSplantation
Other
2021-05-14
EGAS00001005300
Multimodal single-cell and bulk glioma analyses
Other
2021-05-15
EGAS00001005301
Circulating tumor cell copy-number heterogeneity in ALK-rearranged non-small-cell lung cancer resistant to ALK inhibitors
Other
2021-05-15
EGAS00001005303
ChIP-seq in colorectal cancer and paired adjacent normal mucosa
Other
2021-05-17
EGAS00001005304
COVID19 Host Genetic Initiative
Other
2021-05-17
EGAS00001005305
Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Other
2021-05-18
EGAS00001005312
Genomic Rearrangements in Pediatric Cancer
Other
2021-05-19
EGAS00001005313
Genomic Analysis of Focal Nodular Hyperplasia with Associated Hepatocellular Carcinoma Unveils its Malignant Potential
Cancer Genomics
2021-05-19
EGAS00001005314
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Other
2021-05-19
EGAS00001005315
Genome-wide data from Agta hunter-gatherers in Philippines
Other
2021-05-19
EGAS00001005317
Oral microbiome composition of Agta hunter-gatherers (16S)
Other
2021-05-19
EGAS00001005319
Microbiota, Appetite, and Malnutrition in Dutch Community-dwelling older adults
Metagenomics
2021-05-20
EGAS00001005320
Secondary Resistance to Anti-EGFR Therapy by Transcriptional Reprogramming in Patient-Derived Colorectal Cancer Models (hipo_B012)
Cancer Genomics
2021-05-21
EGAS00001005321
Pediatric tumor in a single child of three large nuclear families
Other
2021-05-21
EGAS00001005322
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Other
2021-05-25
EGAS00001005323
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
Other
2021-05-25
EGAS00001005325
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Other
2021-05-26
EGAS00001005326
Immune infiltrate and tumor microenvironment transcriptional programs stratify pediatric osteosarcoma into prognostic groups at diagnosis
Transcriptome Analysis
2021-05-26
EGAS00001005327
Identification of early disease progression in ALK-rearranged lung cancer using circulating tumor DNA analysis (hipo_K34R)
Cancer Genomics
2021-05-26
EGAS00001005328
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Other
2021-05-26
EGAS00001005329
Exome Sequecning of MDS xenografted samples
Other
2021-05-26
EGAS00001005330
An approach for evaluating the effects of dietary fiber polysaccharides on the human gut microbiome and plasma proteome
Metagenomics
2021-05-27
EGAS00001005331
Correction of FFPE artefacts in WGS data
Other
2021-05-27
EGAS00001005332
COVID-19 whole blood transcriptomic analysis
RNASeq
2021-05-27
EGAS00001005339
The mutational landscape of primary central nervous system lymphoma (Hipo H050, A050, XD013)
Other
2021-05-28
EGAS00001005340
Detection and characterization of lung cancer using cell-free DNA fragmentomes
Other
2021-05-28
EGAS00001005341
WGS Leiomyosarcoma subtypes
Whole Genome Sequencing
2021-05-28
EGAS00001005342
Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease
Other
2021-05-31
EGAS00001005343
Single-cell profiling of neoantigen-specific T cells in lung cancers treated with neoadjuvant PD-1 blockade
Other
2021-06-01
EGAS00001005345
Whole genome sequencing based on short and long reads from GM09237 cell line with and without folate depletion
Other
2021-06-01
EGAS00001005346
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Exome Sequencing
2021-06-01
EGAS00001005347
An instructive role for IL7RA in the development of human B-cell precursor leukemia
Other
2021-06-01
EGAS00001005348
Integration of metabolomics, genomics and immune phenotypes reveals the causal roles of metabolites in disease
Population Genomics
2021-06-01
EGAS00001005350
Human gut microbiome in babies with biliary atresia and normal controls
Metagenomics
2021-06-01
EGAS00001005352
Efficacy of CDK4/6i in preclinical models of malignant pleural mesothelioma
Other
2021-06-02
EGAS00001005354
The Xq22.3 contiguous gene deletion syndrome (ATS-ID)
Exome Sequencing
2021-06-02
EGAS00001005355
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Cancer Genomics
2021-06-02
EGAS00001005356
Sequential single-cell transcriptional and protein marker profiling reveals TIGIT as a marker of CD19 CAR-T cell dysfunction in patients with non-Hodgkin’s lymphoma
Other
2021-06-02
EGAS00001005357
The Xq22.3 contiguous gene deletion syndrome (ATS-ID): from genotype to further delineation of the phenotype
Exome Sequencing
2021-06-02
EGAS00001005358
Evaluating CRISPR-based Prime Editing for cancer modeling and CFTR repair in organoids
Whole Genome Sequencing
2021-06-03
EGAS00001005359
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Other
2021-06-03
EGAS00001005360
The genetic scenario of Mercheros: an under-represented population within the Iberian Peninsula
Other
2021-06-03
EGAS00001005361
Nucleosome footprinting in plasma cell-free DNA for diagnosis of ovarian cancer
Other
2021-06-04
EGAS00001005362
Settlement of Polynesia
Other
2021-06-04
EGAS00001005363
Molecular profiles and urinary biomarkers of upper tract urothelial carcinomas associated with aristolochic acid exposure
Other
2021-06-07
EGAS00001005364
Mongolia Western HCC
Other
2021-06-07
EGAS00001005366
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Other
2021-06-07
EGAS00001005367
Whole-genome sequencing of lymphomas in immune-privileged sites
Whole Genome Sequencing
2021-06-08
EGAS00001005368
RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
RNASeq
2021-06-08
EGAS00001005369
Retinal Dystrophy_analysis
Exome Sequencing
2021-06-08
EGAS00001005370
RNAseq from regions of insitu and invasive human mammary ductal disease
RNASeq
2021-06-08
EGAS00001005372
Evidence that ciliary genes contribute to non-syndromic familial tall stature
Exome Sequencing
2021-06-10
EGAS00001005373
Genes___Health_imputed_genotype_dataset
Population Genomics
2021-06-10
EGAS00001005374
Transcriptome and epigenome characterization of BMP signaling effects on H3.3K27M DIPG
Other
2021-06-11
EGAS00001005376
Single-cell RNA sequencing dissects gene-environment interactions on gene expression and regulation in immune cells.
Other
2021-06-11
EGAS00001005377
Spatiotemporal single cell transcriptomic analysis of human gut macrophages reveals multiple functional and niche-specific subsets
RNASeq
2021-06-11
EGAS00001005378
Placental microRNA sequencing data from human placenta
RNASeq
2021-06-11
EGAS00001005379
SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Other
2021-06-11
EGAS00001005380
An analysis of humoral and cellular immune responses following COVID-19 vaccination.
Other
2021-06-11
EGAS00001005382
Single cell copy number and chromatin accessibility in primary multiple myeloma cells
Other
2021-06-11
EGAS00001005384
Mutational impact in liver stem cells under precancerous alcoholic liver, NASH and PSC disease conditions
Whole Genome Sequencing
2021-06-14
EGAS00001005387
Alveolar Rhabdomyosarcoma sequencing data
Other
2021-06-14
EGAS00001005389
Integrative Profiling of T790M Negative EGFR Mutated NSCLC Reveals Pervasive Lineage Transition and Therapeutic Opportunities
Other
2021-06-15
EGAS00001005392
Evaluation of the immune effects of tumor-treating electric fields (TTFields) in GBM patients
RNASeq
2021-06-16
EGAS00001005393
Papua New Guinean Genome Diversity Project
Other
2021-06-16
EGAS00001005394
Functional dissection of inherited non-coding variation influencing multiple myeloma risk
Other
2021-06-16
EGAS00001005395
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Other
2021-06-17
EGAS00001005396
Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Other
2021-06-17
EGAS00001005398
Prevalence of transthyretin amyloidosis in patients with heart failure and no left ventricular hypertrophy
Other
2021-06-17
EGAS00001005399
PELICAN33 longitudinal clinical and autopsy phenomic assessment in lethal metastatic prostate cancer
Other
2021-06-17
EGAS00001005401
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Other
2021-06-18
EGAS00001005402
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Other
2021-06-21
EGAS00001005403
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Other
2021-06-21
EGAS00001005405
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Other
2021-06-21
EGAS00001005407
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Other
2021-06-22
EGAS00001005408
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Other
2021-06-22
EGAS00001005411
Genotyping by OncoArray and Global Screening Array for colorectal cancer risk prediction
Other
2021-06-22
EGAS00001005412
NSCCG CRC GWAS data
Other
2021-06-22
EGAS00001005414
Adult-type Granulosa Cell Tumour of the Ovary
Other
2021-06-22
EGAS00001005417
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Other
2021-06-24
EGAS00001005418
Custom long non-coding RNA capture enhances detection sensitivity in different human sample types.
Other
2021-06-28
EGAS00001005419
Molecular profile of IMFT for the identification of potential druggable targets and biomarkers predicting crizotinib response.
Other
2021-06-28
EGAS00001005420
Mutational landscape of high-grade B-cell lymphoma with MYC-, BCL2 and/or BCL6 rearrangements characterized by whole-exome sequencing
Other
2021-06-28
EGAS00001005421
COIN CRC GWAS data
Other
2021-06-28
EGAS00001005422
Integration of genomics and metabolomics in acute myeloid leukemia
Other
2021-06-28
EGAS00001005423
ANGIOPREDICT - an FP7-funded project enabling personalised medicine for patients with metastatic colorectal cancer.
Other
2021-06-29
EGAS00001005424
Chromothripsis followed by circular recombination drives oncogene amplification in human cancer
Other
2021-06-29
EGAS00001005426
Sequence Data from the phase 2 PrE0505 trial of Durvalumab with First Line Platinum-Pemetrexed for Unresectable Pleural Mesothelioma
Other
2021-06-30
EGAS00001005429
WES on tumor DNA and germline DNA in pediatric cancer
Other
2021-07-01
EGAS00001005430
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Other
2021-07-01
EGAS00001005431
Targeted deep sequencing on Pediatric MDS
Other
2021-07-01
EGAS00001005432
Whole exome sequencing on Pediatric MDS patients
Other
2021-07-01
EGAS00001005433
Single-cell DNA sequencing on Pediatric MDS
Other
2021-07-01
EGAS00001005434
Spatial concordance of DNA methylation classification in diffuse glioma
Other
2021-07-01
EGAS00001005435
Risk alleles of membranous nephropathy and recurrence of the disease on the grafted kidney
Other
2021-07-02
EGAS00001005436
G-SAM: Transcriptional Evolution of Glioblastomas Treated With Standard of Care
Other
2021-07-02
EGAS00001005437
Intellance-2: omics data on recurrent glioblastoma patients participating in the Intellance-2 clinical trial, prior to treatment.
Other
2021-07-02
EGAS00001005442
Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Other
2021-07-05
EGAS00001005443
Targeted-capture sequencing (bam files) of 81 samples of myxofibrosarcoma and 44 matched pairs
Other
2021-07-05
EGAS00001005444
Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs
Other
2021-07-05
EGAS00001005448
SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria
RNASeq
2021-07-06
EGAS00001005450
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Other
2021-07-06
EGAS00001005453
Predictive value of chromosome 18q11.2-q12.1 loss for benefit from bevacizumab in metastatic colorectal cancer; a post-hoc analysis of the randomized controlled trial AGITG-MAX
Other
2021-07-06
EGAS00001005454
IMCISION RNAseq
Other
2021-07-07
EGAS00001005455
Misoprostol-induced high fever GWAS study
Other
2021-07-07
EGAS00001005457
KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population
Other
2021-07-11
EGAS00001005458
A body map of somatic mutagenesis in morphologically normal human tissues (WGS)
Whole Genome Sequencing
2021-07-12
EGAS00001005459
A body map of somatic mutagenesis in morphologically normal human tissues (WES)
Exome Sequencing
2021-07-12
EGAS00001005461
Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children
Other
2021-07-12
EGAS00001005462
ChIP-Seq of TFEB in LT-HSC
Other
2021-07-12
EGAS00001005464
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Other
2021-07-13
EGAS00001005465
Multi-omic single-cell profiling of peripheral blood immune cells from COVID-19 patients and controls.
Other
2021-07-14
EGAS00001005466
IMCISION DNAseq
Other
2021-07-15
EGAS00001005468
An epigenomics time course analysis of covid19 patients from Quebec, Canada
Other
2021-07-16
EGAS00001005470
Genome sequencing of childhood acute leukemia in Iraq
Other
2021-07-19
EGAS00001005472
Epigenetic encoding, heritability and plasticity of glioma transcriptional cell states
Cancer Genomics
2021-07-20
EGAS00001005475
Sequence data for study: Mobilization of tissue-resident memory CD4+ T lymphocytes from bone marrow and their contribution to a systemic secondary immune reaction
Other
2021-07-21
EGAS00001005476
TULIPs decorate the three-dimensional genome of PFA ependymoma
Epigenetics
2021-07-22
EGAS00001005477
Microarray Markers of Response
Transcriptome Analysis
2021-07-22
EGAS00001005478
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Other
2021-07-23
EGAS00001005479
Multi-omics analysis of serial samples from metastatic TNBC patients on PARP inhibitor monotherapy provide insight into rational PARP inhibitor therapy combinations
Other
2021-07-23
EGAS00001005480
Analysis of T-cell receptor clonotypes in tumor micro-environment identifies shared cancer type-specific signatures
Other
2021-07-26
EGAS00001005482
Non-small cell lung cancer proteome subtypes expose targetable oncogenic drivers and immune evasion mechanisms
Other
2021-07-26
EGAS00001005488
MM.1S Single Cell Multiome (ATAC + Gene Expression)
Population Genomics
2021-07-27
EGAS00001005493
A blood atlas of COVID-19 defines hallmarks of disease severity and specificity
Other
2021-07-27
EGAS00001005495
Multi-omics of Richter syndrome
Other
2021-07-27
EGAS00001005496
Correction of a Factor VIII genomic inversion with designer recombinases
Other
2021-07-27
EGAS00001005498
Unraveling the transcriptomic profile of utero-tubal lavage fluid of ovarian cancer patients
Other
2021-07-28
EGAS00001005499
Non-small cell lung cancer sequencing
Cancer Genomics
2021-07-28
EGAS00001005501
CM214 - Biomarker Analysis From the Phase 3 CheckMate 214 Trial of Nivolumab Plus Ipilimumab (N+I) or Sunitinib (S) in Advanced Renal Cell Carcinoma (aRCC)
Other
2021-07-29
EGAS00001005502
Embryonal Rhabdomyosarcoma sequencing data
Other
2021-07-29
EGAS00001005503
Integrated genomic analyses reveal molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma
Other
2021-07-30
EGAS00001005507
Single Cell Transcriptomics of peripheral immune cells pre- and post-Immune Checkpoint Blockade
RNASeq
2021-07-30
EGAS00001005508
Role of cohesin/CTCF in human monocyte differentiation
Other
2021-07-30
EGAS00001005509
A Single-cell Atlas of Progressive TKI Resistance in Chronic Myeloid Leukemia
Other
2021-07-30
EGAS00001005511
Integrated Exome-seq analysis of tumor thrombus
Other
2021-07-30
EGAS00001005512
Integrated RNA-seq analysis of tumor thrombus
Other
2021-07-30
EGAS00001005513
Cancer and germline exomes, and cancer RNA-seq consisiting of FASTQ paired-end reads from melanoma, lung and colon cancer samples
Other
2021-08-02
EGAS00001005514
Methylation clocks - individual colon, small intestine and endometrial crypts
Epigenetics
2021-08-03
EGAS00001005515
Long cell-free DNA molecules in maternal plasma
Other
2021-08-03
EGAS00001005516
A renal cell carcinoma tumorgraft platform to advance precision medicine
Cancer Genomics
2021-08-03
EGAS00001005517
Differential expression profile of gluten-specific T cells identified by single-cell RNA-seq
Other
2021-08-04
EGAS00001005518
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysm in humans
Other
2021-08-04
EGAS00001005520
Immune profiling reveals enrichment of distinct immune signatures in high-risk oral potentially malignant disorders
Other
2021-08-05
EGAS00001005522
The cell free DNA methylome of primary and metastatic prostate tumors
Other
2021-08-05
EGAS00001005523
Pearl study
Cancer Genomics
2021-08-06
EGAS00001005524
Dynamic N6-methyladenosine Epitranscriptomic Landscape in Lung Adenocarcinoma
Other
2021-08-06
EGAS00001005528
CRISPR_single_cell_activation
Other
2021-08-09
EGAS00001005529
Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19
Other
2021-08-09
EGAS00001005530
Pathogenic Neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
Other
2021-08-09
EGAS00001005532
PAH sequencing study
Other
2021-08-09
EGAS00001005533
SJCRH Patient-derived orthotopic xenografts of pediatric brain tumors
Other
2021-08-09
EGAS00001005534
HSC_colony_many_years_post_allogeneic_bone_marrow_transplant___Bait_set_2
Other
2021-08-11
EGAS00001005535
Pancreatic islets PISA RNA-seq samples
Other
2021-08-13
EGAS00001005536
Transcriptome Changes in ASD (NRXN1α+/-) iPSC-derived neurons
Other
2021-08-13
EGAS00001005537
Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Other
2021-08-13
EGAS00001005539
Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Whole Genome Sequencing
2021-08-13
EGAS00001005540
Mitochondrial DNA sequencing
Cancer Genomics
2021-08-15
EGAS00001005541
Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes
Other
2021-08-16
EGAS00001005543
Multipolar zygotic divisions are characterized by parental genome segregation errors
Other
2021-08-17
EGAS00001005544
Investigation of the keratinocytic gene expression pattern in Hidradenitis suppurativa
Other
2021-08-18
EGAS00001005545
Longitudinal Single Cell Atlas of COVID-19 Identifies an Early, Transient Prognostic Signature
Transcriptome Analysis
2021-08-18
EGAS00001005546
Minor intron splicing efficiency increases with the development of lethal prostate cancer
Transcriptome Analysis
2021-08-19
EGAS00001005549
Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Other
2021-08-19
EGAS00001005550
Genomic characterization of retinoblastoma (targeted sequencing)
Other
2021-08-19
EGAS00001005553
Pediatric study using genome sequencing
Other
2021-08-20
EGAS00001005554
DLBCL NGS Genomic Datasets of non-China cohort from Phoenix Clinical Trial
Other
2021-08-22
EGAS00001005556
Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers
Other
2021-08-24
EGAS00001005558
Whole-transcriptome sequencing of hepatocellular carcinoma biopsies (TACE study)
Other
2021-08-24
EGAS00001005559
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Other
2021-08-24
EGAS00001005560
Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Other
2021-08-26
EGAS00001005561
Genomic profiling of Follicular thyroid adenomas and carcinomas using exome-sequencing analyses
Other
2021-08-26
EGAS00001005562
Jagged ends of plasma DNA (human)
Other
2021-08-27
EGAS00001005563
Jagged ends of plasma DNA (mouse)
Other
2021-08-27
EGAS00001005565
Transcriptomes of human CD4+ T lymphocytes - Metabolic project
Other
2021-08-27
EGAS00001005567
The genomic landscape of early stage ovarian high grade serous carcinoma
Other
2021-08-27
EGAS00001005569
Are children born after medical assisted reproduction at greater risk of having an increased de novo mutation rate?
Other
2021-08-31
EGAS00001005572
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Other
2021-09-01
EGAS00001005573
Expression signatures of NGLY1 deficiency
RNASeq
2021-09-01
EGAS00001005577
Spatial Deconvolution of HER2-positive Breast Tumors
Transcriptome Analysis
2021-09-02
EGAS00001005579
Mutation and Microsatellite Burden Predict Response to PD-1 Inhibition in Children with Germline DNA Replication Repair Deficiency: An Observational Registry Study
Cancer Genomics
2021-09-03
EGAS00001005580
Single-cell characterization of anti-LAG3+anti-PD1 treatment in melanoma patients
Other
2021-09-03
EGAS00001005581
RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
Other
2021-09-04
EGAS00001005582
T cell receptors of pathogenic CD4 T cells isolated by using distinct phenotypic markers in celiac disease
Other
2021-09-05
EGAS00001005583
46 patients primary malignant glioma cohort in Chinese population
Other
2021-09-06
EGAS00001005584
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_cytoscan)
Other
2021-09-06
EGAS00001005586
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_oncoscan)
Other
2021-09-06
EGAS00001005587
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_agilent)
Other
2021-09-06
EGAS00001005588
RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors
Other
2021-09-06
EGAS00001005589
Benchmarking DIA-type Proteomics Using Large-Scale Inter-Patient Heterogeneity Dataset
Other
2021-09-06
EGAS00001005591
Synthetic data - Genome in a Bottle
Other
2021-09-07
EGAS00001005592
Serial assessment of measurable residual disease in medulloblastoma liquid biopsies
Other
2021-09-07
EGAS00001005593
Single-cell proteo-genomic reference maps of the human hematopoietic system
Other
2021-09-09
EGAS00001005594
Myeloid cell programming in patients with non-medullary thyroid carcinoma
RNASeq
2021-09-09
EGAS00001005596
Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Other
2021-09-10
EGAS00001005597
Patient data used in FLTseq paper
Other
2021-09-12
EGAS00001005599
Human skeletal muscle CD90+ fibro-adipogenic progenitors are associated with muscle degeneration in type 2 diabetic patients
Transcriptome Analysis
2021-09-13
EGAS00001005600
Osteosarcoma sequencing data
Other
2021-09-13
EGAS00001005601
Absolute copy number fitting from shallow whole genome sequencing data
Whole Genome Sequencing
2021-09-13
EGAS00001005602
Neuroblastoma sequencing data
Other
2021-09-13
EGAS00001005603
High-resolution analysis for urinary DNA jagged ends
Other
2021-09-14
EGAS00001005604
Berlin Neuroblastoma Dataset Update 2021
Cancer Genomics
2021-09-14
EGAS00001005605
Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia
Other
2021-09-14
EGAS00001005606
SNP array study in Autism Spectrum Disorder patients
Other
2021-09-16
EGAS00001005610
WGBS and oxBS-seq for APL
Whole Genome Sequencing
2021-09-18
EGAS00001005612
Transcriptomic consequences of complex rearrangements inv8p23.1 and inv17q21.31 associated with Autism Spectrum Disorders
Other
2021-09-20
EGAS00001005613
APL Oxford Nanopore sequencing - nanome
Whole Genome Sequencing
2021-09-20
EGAS00001005615
Pediatric B-cell precursor acute lymphoblastic leukemia samples with very early relapse
Other
2021-09-21
EGAS00001005616
Combined Metabolic Activators Reduces Liver Fat in Nonalcoholic Fatty Liver Disease Patients
Other
2021-09-21
EGAS00001005617
Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma
Other
2021-09-21
EGAS00001005618
APL nanopore sequencing
Other
2021-09-21
EGAS00001005619
IVF Whole genome prediction
Other
2021-09-21
EGAS00001005620
Multifocal ileal NETs study WGS normal tissue
Whole Genome Sequencing
2021-09-22
EGAS00001005621
Multifocal ileal NETs study WGS HF3J5CCXY
Whole Genome Sequencing
2021-09-22
EGAS00001005622
Multifocal ileal NETs study WGS HF3FKCCXY
Whole Genome Sequencing
2021-09-22
EGAS00001005623
Multifocal ileal NETs study WGS HFG3FCCXY
Whole Genome Sequencing
2021-09-22
EGAS00001005624
Multifocal ileal NETs study WGS HF3NYCCXY
Whole Genome Sequencing
2021-09-22
EGAS00001005625
Multifocal ileal NETs study WGS HFFWLCCXY
Whole Genome Sequencing
2021-09-22
EGAS00001005626
Matched tissue from BRCA1/2 mutation carriers and confirmed non-BRCA mutation carriers
Other
2021-09-23
EGAS00001005627
A microRNA-signature that correlates with cognition and is a target against cognitive decline
Other
2021-09-23
EGAS00001005629
Whole genome sequencing data for 10 hepatocellular carcinomas (HCC) and matched non-tumor liver tissues + optical mapping data for 4 HCC and 3 matched non-tumor liver tissues.
Other
2021-09-24
EGAS00001005632
Genomic Signatures Define Three Subtypes of EGFR-Mutant Stage II-III NSCLC With Distinct Adjuvant Therapy Outcomes
Cancer Genomics
2021-09-28
EGAS00001005633
scRNAseq of human primary nasal epithelium differentiated at air-liquid interface exposed to SARS-CoV2
Other
2021-09-28
EGAS00001005634
Single-cell RNA-seq of bronchoalveolar lavage (BAL) fluid of late stage severe COVID-19 patients
Other
2021-09-29
EGAS00001005637
ADAPTeR Study: RNAseq data from ccRCC patients
Other
2021-09-30
EGAS00001005638
ADAPTeR Study: WES data from ccRCC patients
Other
2021-09-30
EGAS00001005639
ADAPTeR Study: TCRseq data from ccRCC patients
Other
2021-09-30
EGAS00001005640
ADAPTeR Study: scRNA and scTCR data from TILs from two ccRCC patients treated with anti-PD1
Other
2021-09-30
EGAS00001005641
Proteom characterization in primary colorectal cancer and corresponding liver metastasis
Other
2021-10-01
EGAS00001005647
Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target
Other
2021-10-01
EGAS00001005648
The genomic landscape of serrated lesion of the colorectum
Other
2021-10-04
EGAS00001005649
Variation and transmission of the human gut microbiota across generations - shotgun data
Other
2021-10-04
EGAS00001005651
Variation and transmission of the human gut microbiota across generations - 16S data
Other
2021-10-04
EGAS00001005653
PIK3CA mutation in a case of CTNNB1 mutant sinonasal glomangiopericytoma
Exome Sequencing
2021-10-04
EGAS00001005655
RNAseq in blood CD34+ cells
Other
2021-10-05
EGAS00001005656
Pre-neoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma
Other
2021-10-06
EGAS00001005661
Whole-exome sequencing of HCC patients undergoing sorafenib treatment
Other
2021-10-06
EGAS00001005662
RNA-sequencing of HCC patients undergoing sorafenib treatment
Other
2021-10-06
EGAS00001005665
DGCR8 and the six hit, three-step model of schwannomatosis
Other
2021-10-07
EGAS00001005669
SudanMitoSeq: Sudanese mitochondrial sequencing
Other
2021-10-13
EGAS00001005673
Whole exome sequencing of Congenital Cataract
Other
2021-10-15
EGAS00001005675
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Other
2021-10-15
EGAS00001005676
Identification of biomarkers of response to preoperative talazoparib monotherapy in treatment naïve gBRCA+ breast cancers
Other
2021-10-18
EGAS00001005677
Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Other
2021-10-18
EGAS00001005678
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Other
2021-10-18
EGAS00001005679
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Other
2021-10-18
EGAS00001005680
Targeted sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas
Other
2021-10-18
EGAS00001005681
Disturbed trophoblast transition links early fetal to maternal syndrome progression in pre-eclampsia
Transcriptome Analysis
2021-10-18
EGAS00001005684
MM samples for epigenomic translocation of H3K4me3 broad domains following super-enhancer hijacking
Other
2021-10-18
EGAS00001005685
Whole Exome Sequencing of Localized Prostate Cancer Patients
Other
2021-10-18
EGAS00001005686
MNM - Temporal variability in Quantitative Microbiome Profiles
Other
2021-10-18
EGAS00001005687
Pediatric HGG WES and RNA-Seq
Other
2021-10-19
EGAS00001005689
Ewing's sarcoma sequencing data
Other
2021-10-19
EGAS00001005690
Wilm's tumor sequencing data
Other
2021-10-19
EGAS00001005691
Single-nucleus transcriptomic profiling of aging Down Syndrome brains
Other
2021-10-19
EGAS00001005692
Signals of positive selection in Peruvians from three ecological regions
Other
2021-10-19
EGAS00001005696
COVID_19_Challenge_Project_Single_Cell_Profiling
Other
2021-10-21
EGAS00001005697
Single-cell RNA sequencing of a PBMC sample collected from a male with 45,X/48,XYYY karyotype
Transcriptome Analysis
2021-10-21
EGAS00001005698
Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients.
Other
2021-10-21
EGAS00001005700
Genomic profile of sporadic multiple meningiomas
Other
2021-10-21
EGAS00001005702
Human genomic and phenotypic synthetic data for the study of rare diseases
Other
2021-10-22
EGAS00001005704
BARIA baseline first 100 individuals transcriptomes
Other
2021-10-25
EGAS00001005720
DERMATLAS__Porocarcinoma_WES
Other
2021-10-26
EGAS00001005721
DERMATLAS__Porocarcinoma_RNAseq
Other
2021-10-26
EGAS00001005728
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Other
2021-10-26
EGAS00001005729
Barrett esophagus phenotypic evolution study
Whole Genome Sequencing
2021-10-26
EGAS00001005730
Human and rat skeletal muscle multi-omic profiling
Other
2021-10-26
EGAS00001005731
DNA methylation and Panel sequencing for pancreatic neuroendocrine carcinomas (PanNECs) and pancreatic neuroendocrine tumors (PanNETs)
Cancer Genomics
2021-10-26
EGAS00001005732
scRNA-seq of LN and lymphoma stroma
Other
2021-10-27
EGAS00001005734
Molecular_risk_stratification_in_patients_with_T1_colorectal_cancer_WES
Other
2021-10-28
EGAS00001005735
Unifying recovery dynamics in heterogeneous diseases exemplified by COVID-19
Other
2021-10-28
EGAS00001005736
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Other
2021-10-29
EGAS00001005737
Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Other
2021-10-29
EGAS00001005738
Genome-wide cell-free DNA termini in patients with cancer
Other
2021-10-29
EGAS00001005739
cfDNA and CDX/PDX methylation profiling in SCLC
Other
2021-10-29
EGAS00001005740
Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models enables specific monitoring of tumour-derived extracellular RNA
RNASeq
2021-10-29
EGAS00001005743
Comparative analysis of RAF depletion vs. MAPK inhibition
RNASeq
2021-10-29
EGAS00001005744
IN UTERO ORIGIN OF MYELOFIBROSIS PRESENTING IN ADULT MONOZYGOTIC TWINS AFTER A PROLONGED DISEASE LATENCY
Cancer Genomics
2021-10-29
EGAS00001005745
Stereotyped B-cell responses are linked to IgG constant region polymorphisms in multiple sclerosis
Other
2021-10-30
EGAS00001005746
Proteogenomics of chronic lymphocytic leukemia
Other
2021-10-31
EGAS00001005747
Genome-wide cell-free DNA termini in patients with cancer
Other
2021-11-01
EGAS00001005748
The effect of pre-analytical and physiological variables on cell-free DNA fragmentation
Other
2021-11-01
EGAS00001005752
Multi-omic dataset of neuroendocrine neoplasm organoids
Other
2021-11-03
EGAS00001005753
Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
Other
2021-11-03
EGAS00001005755
Targeted sequencing data and shallow whole genome sequencing data of Follicular lymphoma.
Other
2021-11-04
EGAS00001005757
A critical spotlight on the paradigms of FFPE-DNA sequencing
Other
2021-11-05
EGAS00001005758
Detection of Cancer Mutations by Urine Liquid Biopsy in Bladder Cancer Patients
Other
2021-11-05
EGAS00001005759
DERMATLAS__Poroma_RNAseq
Other
2021-11-05
EGAS00001005760
Genomics of pediatric myeloid neoplasms
Other
2021-11-05
EGAS00001005761
Exome sequencing
Other
2021-11-07
EGAS00001005764
JEM 20211004R
Exome Sequencing
2021-11-08
EGAS00001005765
Whole-exome sequencing of paired tumour/blood of 58 T1 stage bladder cancer patients
Other
2021-11-08
EGAS00001005766
Targeted sequencing of paired tumour/blood of 78 Ta stage bladder cancer patients
Other
2021-11-08
EGAS00001005767
Targeted sequencing of paired tumour/blood of 34 T1 stage bladder cancer patients
Other
2021-11-08
EGAS00001005769
Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer
Other
2021-11-09
EGAS00001005770
Obesity and hyperinsulinemia drive adipocytes to activate a cell cycle program and senesce
RNASeq
2021-11-10
EGAS00001005772
Acne GWAS meta-analysis
Other
2021-11-10
EGAS00001005773
Multi-omic analysis of cell-of-origin and epigenomic state in pediatric H3K27M gliomas
Other
2021-11-10
EGAS00001005781
Clinical impact of immune checkpoint inhibitor (ICI) response, DNA damage repair (DDR) gene mutations and immune-cell infiltration in subtypes of metastatic melanoma
Other
2021-11-11
EGAS00001005782
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers
Other
2021-11-11
EGAS00001005783
Deep whole genome ctDNA chronology of treatment-resistant prostate cancer
Cancer Genomics
2021-11-11
EGAS00001005784
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Other
2021-11-12
EGAS00001005786
Extensive three-dimensional intratumor proteomic heterogeneity revealed by multiregion sampling in high-grade serous ovarian tumor specimens
Other
2021-11-12
EGAS00001005787
Resolving the immune landscape of human prostate at a single cell level in health and cancer
Other
2021-11-14
EGAS00001005788
Myeloma methylation
Other
2021-11-14
EGAS00001005791
Mutations in ALK signaling pathways conferring resistance to ALK inhibitor treatment lead to collateral vulnerabilities in neuroblastoma cells
Cancer Genomics
2021-11-15
EGAS00001005793
NOTCH-mutations drive immune-escape mechanisms in B cell malignancies
Other
2021-11-16
EGAS00001005797
Mexican Biobank Project
Other
2021-11-18
EGAS00001005798
Persistence of circulating tumor DNA in breast cancer patients during neoadjuvant treatment is a significant predictor of poor tumor response
Other
2021-11-18
EGAS00001005807
RNA-seq data from 27 glioblastoma samples
RNASeq
2021-11-19
EGAS00001005808
RNA sequencing data of in vitro differentiated megakaryocyte cells transduced with E527K and WT SRC
Other
2021-11-19
EGAS00001005810
Amplified EPOR/JAK2 genes define a unique subtype of acute erythroid leukemia
Other
2021-11-20
EGAS00001005812
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Cancer Genomics
2021-11-22
EGAS00001005815
Sequencing data for CLL patients
Other
2021-11-24
EGAS00001005816
B cell receptor repertoire kinetics after SARS-CoV-2 infection and vaccination
Other
2021-11-24
EGAS00001005818
Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia
RNASeq
2021-11-26
EGAS00001005819
Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia
RNASeq
2021-11-26
EGAS00001005820
Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia
Exome Sequencing
2021-11-26
EGAS00001005822
DNA sequencing for human normal endometrial glands
Other
2021-11-29
EGAS00001005826
Failure of Differentiation of the Rhombic Lip Constitutes Medulloblastoma
Other
2021-11-29
EGAS00001005827
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Cancer Genomics
2021-11-29
EGAS00001005828
Molecular profiling of DLBCL patients treated in the PETAL trial
Other
2021-11-29
EGAS00001005829
Whole exome sequencing of 12 NSCLC samples from 4 patients at MDACC
Other
2021-11-29
EGAS00001005830
Full blood mRNA sequencing of myotonic dystrophy type 1 patients after cognitive behavioural therapy
Other
2021-11-29
EGAS00001005832
DNA methylation analysis on PBL obtained from male patients with UC-PSC, UC and HC
Other
2021-11-30
EGAS00001005833
Paired data of primary and relapse central nervous system lymphoma and testicular lymphoma
Other
2021-11-30
EGAS00001005835
NLG-LBC-05 ctDNA
Other
2021-11-30
EGAS00001005836
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Other
2021-11-30
EGAS00001005840
SPECTA RP-1759-AYA Sarcoma cohort
Other
2021-12-02
EGAS00001005846
Orthotopic murine Group 3 medulloblastoma in C57Bl/6 mice treated with saline, cyclophosphamide or gemcitabine
RNASeq
2021-12-03
EGAS00001005847
Orthotopic murine Group 3 medulloblastoma in C57Bl/6 mice treated with sham or craniospinal irradiation
RNASeq
2021-12-03
EGAS00001005848
Searching for genetic modulators of the phenotypic heterogeneity in Brugada Syndrome
Exome Sequencing
2021-12-03
EGAS00001005849
Optimisation of CITE-seq on liquid and solid tissues
Other
2021-12-03
EGAS00001005850
TB-DAR Whole Genome Sequencing Study
Other
2021-12-03
EGAS00001005861
Single-nuclei gene-expression analysis of pheochromocytoma and paraganglioma links tumor subtypes with tumor microenvironment
Other
2021-12-06
EGAS00001005863
Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Other
2021-12-07
EGAS00001005864
Nascent transcriptome in T-ALL bone marrow
Other
2021-12-07
EGAS00001005865
Paired healthy & tumor organoid Biobank _B15PON
Cancer Genomics
2021-12-08
EGAS00001005866
RNA-seq following miR-130a knock-down (KD) in Flag-tag AML1-ETO Kasumi-1 cells
Other
2021-12-08
EGAS00001005867
CUT&RUN of AML1-ETO binding occupancy following miR-130a KD in Kasumi-1 cells
Other
2021-12-08
EGAS00001005868
RNA-seq following miR-130a overexpression (OE) in human CD34+cord blood cells
Other
2021-12-08
EGAS00001005869
RNA-seq following TBL1XR1 KD in human CD34+CD38- cord blood cells
Other
2021-12-08
EGAS00001005870
tFL with a PMBL GE signature
Other
2021-12-08
EGAS00001005872
Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing
Other
2021-12-08
EGAS00001005873
Effects of nucleases on cell-free extrachromosomal circular DNA
Other
2021-12-09
EGAS00001005874
Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Other
2021-12-09
EGAS00001005875
Molecular and clinical effects of selective TYK2 inhibition with deucravacitinib in psoriasis
Other
2021-12-13
EGAS00001005876
Comprehensive characterization of pre- and post-treatment samples of breast cancer reveal potential mechanisms of chemotherapy resistance
Other
2021-12-13
EGAS00001005878
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
Other
2021-12-13
EGAS00001005879
Deciphering RBP - alternative splicing networks in ALS iPSC-MN: patient and control datasets
Other
2021-12-13
EGAS00001005880
Deciphering RBP - alternative splicing networks in ALS iPSC-MN: TDP-43, NOVA1, NOVA2 and RBFOX2 eCLIP-seq
Other
2021-12-13
EGAS00001005881
Deciphering RBP - alternative splicing networks in ALS iPSC-MN: NOVA1 gain and loss of function systems
Other
2021-12-13
EGAS00001005887
Patient-derived tumor organoids for personalized medicine in a rare case of hepatocellular carcinoma with neuroendocrine differentiation.
Other
2021-12-14
EGAS00001005891
Comparison of fresh and slow-frozen cancer samples for different applications
Other
2021-12-16
EGAS00001005892
Functional Mapping of AKT Signaling and Biomarkers of Response From the FAIRLANE Trial of Neoadjuvant Ipatasertib Plus Paclitaxel for Triple-Negative Breast Cancer
Other
2021-12-17
EGAS00001005893
Initial cohort of 500 solid tumors screened for Basket of Baskets
Cancer Genomics
2021-12-17
EGAS00001005895
INSIGHT: VHL Case Report
Other
2021-12-17
EGAS00001005897
Origins and timing of emerging lesions in advanced renal cell carcinoma
Other
2021-12-19
EGAS00001005899
Targeted de novo phasing and long-range assembly by template mutagenesis
Population Genomics
2021-12-20
EGAS00001005900
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort
Other
2021-12-21
EGAS00001005902
Whole genome and exome sequencing data of invasive micropapillary carcinoma of breast
Other
2021-12-22
EGAS00001005904
A transcriptome atlas of human skeletal muscles
Other
2021-12-23
EGAS00001005905
Reproducibility of 10x Genomics single cell RNA sequencing method in the immune cell environment
Other
2021-12-27
EGAS00001005906
Exome-wide mutation analysis of cell-free DNA to simultaneously monitor the full spectrum of cancer treatment outcomes
Other
2021-12-30
EGAS00001005908
Transcriptome analysis of endometrial organoids derived from patients with Mayer-Rokitansky-Küster-Hauser syndrome
Other
2021-12-30
EGAS00001005909
Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
Other
2022-01-04
EGAS00001005910
Genome-wide genotype data for 1,433 ni-Vanuatu
Other
2022-01-04
EGAS00001005911
Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosissusceptibility
Other
2022-01-05
EGAS00001005912
Sequencing of an organoid biobank for childhood soft tissue sarcoma.
Other
2022-01-05
EGAS00001005914
Target gene sequencing for human normal endometrial glands
Other
2022-01-06
EGAS00001005926
Genomic determination for Homologous Recombination Deficiency (HRD) by shallow Whole Genome Sequencing (sWGS)
Other
2022-01-06
EGAS00001005931
COVID-19 Severity of First Wave of Infection for Severe Patients in Madrid
Other
2022-01-07
EGAS00001005932
Methylation profiling of osteoblastomas and their mimics
Other
2022-01-07
EGAS00001005933
Myoepithelial progenitors as founder cells of hyperplastic human breast lesions upon PIK3CA transformation
Other
2022-01-09
EGAS00001005935
The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Other
2022-01-10
EGAS00001005937
Paired healthy & tumor organoid Biobank _B16PON
Other
2022-01-11
EGAS00001005939
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Other
2022-01-12
EGAS00001005940
Molecular analysis in bowel malignancies in cancer survivors vs. primary malignancies
Cancer Genomics
2022-01-13
EGAS00001005941
T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients
Other
2022-01-14
EGAS00001005945
Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Other
2022-01-18
EGAS00001005947
Patient-derived organoids_Vumc
Cancer Genomics
2022-01-18
EGAS00001005948
RNA-seq on patient-derived, stage II, CRC cell lines
Other
2022-01-18
EGAS00001005949
Overexpression of the miR-17-92 cluster in colorectal adenoma organoids induces a carcinoma-like genotype
Cancer Genomics
2022-01-18
EGAS00001005950
The Proteogenomic Subtypes of Acute Myeloid Leukemia
Other
2022-01-18
EGAS00001005951
RNA sequencing of 12 NSCLC samples from 4 patients at MDACC
Other
2022-01-18
EGAS00001005952
Tumor-intrinsic expression of the autophagy gene Atg16l1 suppresses anti-tumor immunity in colorectal cancer
Other
2022-01-20
EGAS00001005953
Targeted sequencing of diffuse large B-cell lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Other
2022-01-20
EGAS00001005954
RNA-sequencing data from metastatic Castration-Resistant Prostate Cancer (mCRPC)
Other
2022-01-20
EGAS00001005955
Monocyte and macrophage lipid accumulation results in downregulated type-I interferon responses
Other
2022-01-20
EGAS00001005957
Oesophageal adenocarcinoma whole exome and RNA-seq raw sequencing data
Cancer Genomics
2022-01-21
EGAS00001005963
Ductal keratin 15+ luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
Other
2022-01-25
EGAS00001005965
TLR7 variants in human lupus patients
Exome Sequencing
2022-01-26
EGAS00001005969
LifeLines-NEXT pilot study
Other
2022-01-28
EGAS00001005970
Genome analysis of early onset sporadic rectal cancer
Cancer Genomics
2022-01-28
EGAS00001005971
Evaluating the immune response in treatment-naive hospitalised patients with influenza and COVID-19
Other
2022-01-28
EGAS00001005972
H3Africa - Consortium WGS
Other
2022-01-28
EGAS00001005973
ENCORAFENIB COMBINED WITH BINIMETINIB FOR BRAFV600E-MUTATED RELAPSED/REFRACTORY MULTIPLE MYELOMA: THE PHASE II GMMG-BIRMA TRIAL (Hipo_K08K)
Other
2022-01-28
EGAS00001005974
An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs
Other
2022-01-28
EGAS00001005975
850k Methyome analysis of snap frozen or FFPE stored human MBM
Other
2022-01-29
EGAS00001005976
Molecular programs of melanoma brain metastases (MBM)
Other
2022-01-29
EGAS00001005978
Bulk RNA sequencing of Singapore colorectal cancer patients (SG-BULK)
Other
2022-01-31
EGAS00001005980
Unravelling the contribution of HIF pathway and its therapeutic potential in human AML leukemia-initiating cells
Other
2022-01-31
EGAS00001005981
Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer
Other
2022-01-31
EGAS00001005982
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Other
2022-01-31
EGAS00001005983
Epithelioid sarcoma sequencing data
Other
2022-01-31
EGAS00001005984
The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer
Other
2022-02-01
EGAS00001005985
The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals.
Other
2022-02-01
EGAS00001005986
Biallelic HMBS Inactivation Defines a Homogenous Clinico-Molecular Subtype of Hepatocellular Carcinoma
Other
2022-02-01
EGAS00001005992
Cell-free DNA and bone marrow samples from myelodysplastic syndromes
Other
2022-02-03
EGAS00001005993
Host genotyping data from Dutch adult bacterial meningitis patients and linked bacterial genome sequences
Other
2022-02-03
EGAS00001005995
To determine the genomic profile of Triple Negative Breast Cancer patient-derived xenografts (PDX cohort)
Other
2022-02-03
EGAS00001005997
Bioinformatics analysis of chimerism in monochorionic dizygotic twins
Other
2022-02-04
EGAS00001006001
Combination of ribociclib and gemcitabine for the treatment of medulloblastoma
Other
2022-02-04
EGAS00001006002
Specific BRCA and immune configurations determine optimal response to platinum-based chemotherapy in triple negative breast and ovarian carcinomas (COH_TNBC_RNAseq)
Other
2022-02-04
EGAS00001006004
Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab
Other
2022-02-05
EGAS00001006005
A Proteogenomic Analysis of Clear Cell Renal Cell Carcinoma in a Chinese Population
Other
2022-02-05
EGAS00001006006
Whole Exome sequencing of colorectal cancer patients (SG-BULK)
Other
2022-02-07
EGAS00001006007
Genomic and transcriptome analysis for intrahepatic cholangiocarcinoma
Cancer Genomics
2022-02-07
EGAS00001006008
PROJET DREPANOCYTOSE ET PALUDISME
Other
2022-02-07
EGAS00001006009
CCL22 chemokine mutations drive natural killer cell lymphoproliferative disease by biasing GPCR signaling
Other
2022-02-07
EGAS00001006010
Human genome-wide variations in the Massim region
Other
2022-02-07
EGAS00001006011
Genomic diversity of Vietnamese
Other
2022-02-07
EGAS00001006012
To determine the transcriptional profiles of Ovarian carcinomas (UW cohort)
Other
2022-02-07
EGAS00001006013
Single cell RNA sequencing of colorectal cancer patients (CRC-SG1)
Other
2022-02-08
EGAS00001006015
DNA methylation profiles of samples included in the EORTC 26091 TAVAREC trial
Epigenetics
2022-02-08
EGAS00001006016
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (RNA-seq)
Other
2022-02-09
EGAS00001006017
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq)
Other
2022-02-09
EGAS00001006019
Disease specific alterations in the olfactory mucosa of patients with Alzheimer’s disease
Other
2022-02-09
EGAS00001006020
Methylome sequencing of cell-free DNA and RRBS of solid tissue
Other
2022-02-09
EGAS00001006022
Whole-exome sequencing of glioblastomas with long-term relapse interval
Other
2022-02-10
EGAS00001006024
Application of high-throughput, high-depth, targeted single-nucleus DNA sequencing in pancreatic cancer
Other
2022-02-10
EGAS00001006025
Papuan Y chromosome Diversity Panel
Other
2022-02-11
EGAS00001006027
Targeted analysis of cell-free circulating tumor DNA is suitable for early relapse and actionable target detection in patients with neuroblastoma
Cancer Genomics
2022-02-11
EGAS00001006028
IYDP Indonesian Y chromosome Diversity Project
Other
2022-02-11
EGAS00001006030
Whole genome sequencing of colorectal cancer patients (SG-BULK-1)
Other
2022-02-13
EGAS00001006031
Genomewide copy number alteration screening of circulating plasma DNA
Other
2022-02-13
EGAS00001006033
Genome-wide DNA Methylation Data from Illumina HumanMethylationEPIC arrays for whole blood samples from 403 healthy individuals
Other
2022-02-14
EGAS00001006034
The clinical utility of genomics in childhood cancer extends beyond targetable mutations
Other
2022-02-15
EGAS00001006035
WGS of iPSC from TOF patients with/without DG and healthy control
Whole Genome Sequencing
2022-02-15
EGAS00001006036
RNASeq of PAX4 KO vs WT in 7 stages of differentiation from human iPSCs to BLC
Other
2022-02-15
EGAS00001006037
The KATHERINE study of adjuvant trastuzumab emtansine in HER2-positive breast cancer: analysis of patients with HER2-negative residual invasive disease on re-testing
Other
2022-02-16
EGAS00001006038
GINS3 fibroblast RNAseq
Other
2022-02-16
EGAS00001006039
Whole Genome sequencing of colorectal cancer patients (SG-BULK-2)
Other
2022-02-17
EGAS00001006040
Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer
Other
2022-02-17
EGAS00001006042
Anti-Cancer Therapies Induce Mutations in Adult Stem Cells in a Tissue-Specific Manner
Forensic or Paleo-genomics
2022-02-18
EGAS00001006043
Whole Exome Sequencing PPGL
Other
2022-02-18
EGAS00001006044
Transcriptome Sequencing PPGL
Other
2022-02-18
EGAS00001006045
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Other
2022-02-18
EGAS00001006048
To determine the genomic profiles of Ovarian carcinomas (UW cohort)
Other
2022-02-18
EGAS00001006049
Single cell RNA sequencing of colorectal cancer patients (KUL3/KUL5)
Other
2022-02-21
EGAS00001006050
CIRdb: Array genotype data
Other
2022-02-21
EGAS00001006051
WGS of gastric cancer in the Japanese population (81 gastric cancers of NCC)
Other
2022-02-22
EGAS00001006052
Microenvironment subtypes and association with tumor cell mutations and antigen expression in follicular lymphoma
Other
2022-02-22
EGAS00001006053
Insights from genome-wide data from Thailand and Laos
Other
2022-02-22
EGAS00001006055
Oncogenic cooperation in a human de novo T-ALL model
Other
2022-02-22
EGAS00001006056
Whole Genome sequencing of colorectal cancer patients (SG-BULK-3)
Other
2022-02-23
EGAS00001006058
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Other
2022-02-24
EGAS00001006059
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Other
2022-02-24
EGAS00001006060
Genetics of non-syndromic idiopathic autism spectrum disorders in India
Other
2022-02-25
EGAS00001006062
A multi-center genome-wide association study for nasopharyngeal carcinoma
Population Genomics
2022-02-28
EGAS00001006063
Enhanced cortical neural stem cell identity through SMAD/WNT inhibition in human cerebral organoids facilitates emergence of outer radial glial cells
Other
2022-02-28
EGAS00001006068
Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies unique proteotypes associated with patient outcomes
Other
2022-02-28
EGAS00001006069
Genomic landscape of malignant peripheral nerve sheath tumor (MPNST)
Other
2022-02-28
EGAS00001006072
Clear cell sarcoma sequencing data
Other
2022-03-01
EGAS00001006073
Genomic and transcriptomic analysis of baseline PDAC patients' tumors from the OXIRI phase 1b clinical trial
Other
2022-03-02
EGAS00001006085
To determine the genomic profiles of Triple Negative Breast Cancers (COH cohort)
Other
2022-03-03
EGAS00001006088
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Cancer Genomics
2022-03-03
EGAS00001006089
Genomic History of Siberia
Population Genomics
2022-03-03
EGAS00001006090
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Other
2022-03-03
EGAS00001006091
Res1_H23_exp1_MC_04_03_22
Cancer Genomics
2022-03-04
EGAS00001006092
Res1_HT29_exp1_MC_02_03_22
Cancer Genomics
2022-03-04
EGAS00001006093
Res1_HT29_exp2_MC_03_03_22
Cancer Genomics
2022-03-04
EGAS00001006096
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data)
Cancer Genomics
2022-03-04
EGAS00001006098
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data)
Cancer Genomics
2022-03-04
EGAS00001006101
Whole Genome sequencing of colorectal cancer patients (SG-BULK-4)
Other
2022-03-05
EGAS00001006102
A genome-wide association study for nasopharyngeal carcinoma in Hong Kong population
Population Genomics
2022-03-06
EGAS00001006103
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Other
2022-03-07
EGAS00001006105
Profiling of 27 type 2 diabetes GWAS loci using next-generation (NG) capture C in a human beta-cell model
Other
2022-03-08
EGAS00001006106
Single cell analyses of transcriptome and epigenome in neuroblastoma infiltrated bone marrow
Other
2022-03-08
EGAS00001006107
Adult B-precursor acute lymphoblastic leukemia transcriptomes
Other
2022-03-09
EGAS00001006112
RNAseq Iron-Treated iPSC-derived Microglia
Other
2022-03-10
EGAS00001006113
Spatio-temporal analysis of prostate tumors in situ suggests pre-existence of treatment-resistant clones
Other
2022-03-10
EGAS00001006114
Whole Genome sequencing of colorectal cancer patients (SG-BULK-5)
Other
2022-03-11
EGAS00001006115
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Other
2022-03-11
EGAS00001006116
Genomic History of the Solomon Islands
Other
2022-03-11
EGAS00001006117
CDK4 phosphorylation predicts high sensitivity of malignant pleural mesotheliomas to CDK4/6 inhibition
Other
2022-03-11
EGAS00001006118
Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer
Other
2022-03-12
EGAS00001006119
Total RNA sequencing of RNA from testicular tissue
RNASeq
2022-03-12
EGAS00001006120
Stromal-induced epithelial-mesenchymal transition induces drug resistance in acute lymphoblastic leukemia
Other
2022-03-14
EGAS00001006122
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Cancer Genomics
2022-03-14
EGAS00001006123
Genetic immune escape landscape in primary and metastatic cancer
Other
2022-03-15
EGAS00001006124
Spatial atlas of clonal copy number alterations in co-existing benign and malignant tissue
Other
2022-03-15
EGAS00001006125
Engineered Human Primary T Cell transcriptome study
Other
2022-03-15
EGAS00001006126
early-stage ESCC sequencing study
Other
2022-03-16
EGAS00001006127
RNASeq of Calcoco2 in beta and fat cell lines
Other
2022-03-16
EGAS00001006132
Denisova admixture in Southeast Asia and Oceania
Other
2022-03-17
EGAS00001006133
Discriminating Th17.1 cell driven sarcoidosis-like inflammation from relapse after anti-BCMA CAR T cells in multiple myeloma
Other
2022-03-18
EGAS00001006134
Longitudinal monitoring of disease burden and response using ctDNA from dried blood spots in xenograft models
Whole Genome Sequencing
2022-03-18
EGAS00001006135
Stage-specific gene and transcript dynamics in human male germ cells
Other
2022-03-18
EGAS00001006136
single cell RNA-seq and ATAC-seq of human fetal forebrain tissue
Other
2022-03-19
EGAS00001006138
Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G4C2)n expression in C9orf72 ALS/FTD
Other
2022-03-21
EGAS00001006139
The transcriptomic response of skeletal muscle in life-long high-level trained and untrained men and women after acute exercise
Other
2022-03-21
EGAS00001006140
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Other
2022-03-21
EGAS00001006141
Integrated single-cell profiling dissects cell-state-specific enhancer landscapes of human tumor infiltrating T cells.
Epigenetics
2022-03-21
EGAS00001006142
Genome-wide cell-free DNA termini in patients with cancer
Other
2022-03-22
EGAS00001006143
FACS sorting of ploidy populations in an undifferentiated soft tissue sarcoma for RRBS
Other
2022-03-22
EGAS00001006144
USARC 10X Genomics Single Cell DNA Sequencing Data
Other
2022-03-22
EGAS00001006147
Whole exome sequencing study of cholesteatoma patients from affected families
Other
2022-03-23
EGAS00001006148
Genomic profiling of metastatic basal cell carcinoma reveals candidate drivers of disease and therapeutic targets
Cancer Genomics
2022-03-24
EGAS00001006154
Detection of uniparental disomy from genome sequencing of family trio
Other
2022-03-24
EGAS00001006155
Detection of maternal DNA contamination in the placenta
Other
2022-03-24
EGAS00001006157
miRNA regulation of monocyte expressed inflammatory genes in patients with inflammatory bowel disease
Transcriptome Analysis
2022-03-25
EGAS00001006158
Exome sequencing in CLL re-treated with venetoclax
Exome Sequencing
2022-03-26
EGAS00001006159
Epigenomic data of Human muscle stem cell
Other
2022-03-28
EGAS00001006161
Enhancer profiling to identify identifies epigenetic markers of endocrine resistance in metastatic castration resistant prostate cancer patients
Epigenetics
2022-03-28
EGAS00001006164
Validation of a targeted sequencing panel for multiple myeloma
Cancer Genomics
2022-03-29
EGAS00001006166
Molecular landscape of blastic plasmacytoid dendritic cell neoplasm
Other
2022-03-30
EGAS00001006167
LCM-ATACseq on human lung macrophages
Other
2022-03-30
EGAS00001006168
LCM-RNAseq on human lung macrophages
Other
2022-03-30
EGAS00001006169
Res1_PC9_exp1_MC_29_03_22
Cancer Genomics
2022-03-30
EGAS00001006170
Res1_PC9_exp2_MC_01_04_22
Cancer Genomics
2022-03-30
EGAS00001006172
A Dose Escalation Study of Efmarodocokin Alfa (UTTR1147A) in Healthy Volunteers and Patients with Ulcerative Colitis
Other
2022-03-31
EGAS00001006173
Phase 1 CX-5461 Trial (Canadian Cancer Trials Group Trial IND.231)
Other
2022-03-31
EGAS00001006174
Small molecule inhibitors of LOXL synergize with 5-AZA to restore erythropoiesis in myeloid neoplasms
Other
2022-03-31
EGAS00001006175
Characterization of Cell Free Plasma Methyl-DNA From Xenografted Tumors to Guide the Selection of Diagnostic Markers for Early-Stage Cancers
Other
2022-04-01
EGAS00001006176
Genomic insights into the population history of the Resande or Swedish Travellers
Other
2022-04-01
EGAS00001006184
Mapping genetic effects on cell type-specific chromatin accessibility using single nucleus ATAC-seq
Other
2022-04-05
EGAS00001006185
Variants from a subset of genes from WES of adult AML patient samples
Other
2022-04-05
EGAS00001006186
Dual spatially resolved transcriptomics for human host-pathogen colocalization studies in FFPE tissue sections
Other
2022-04-05
EGAS00001006187
Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis
Other
2022-04-05
EGAS00001006191
Molecular and clinical diversity in primary central nervous system lymphoma: a LOC Network study
Other
2022-04-06
EGAS00001006195
RNA sequencing of AD, MCI and control OM cells
Other
2022-04-07
EGAS00001006196
Androgen receptor blockade promotes response to BRAF/MEK-targeted therapy
Other
2022-04-07
EGAS00001006198
Heat selection enables highly scalable methylome profiling in cell-free DNA for noninvasive monitoring of cancer patients
Other
2022-04-11
EGAS00001006200
Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
Other
2022-04-11
EGAS00001006201
Serum proteomics of aortic diseases
Other
2022-04-11
EGAS00001006202
Separation, characterization, and identification of individuals from multi-person blood mixtures with single cell transcriptome sequencing and a novel bioinformatics pipeline
Other
2022-04-11
EGAS00001006203
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Other
2022-04-12
EGAS00001006204
Molecular Classification of Hormone Sensitive and Castration Resistant prostate cancer, using non-negative matrix factorization molecular subtyping
Other
2022-04-13
EGAS00001006205
Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors
Other
2022-04-13
EGAS00001006206
ATAC Sequencing of 4 CLL patient samples
Other
2022-04-14
EGAS00001006211
Gremlin 1 + fibroblastic niche maintains dendritic cell homeostasis in lymphoid tissues
Other
2022-04-16
EGAS00001006212
WXS and RNA-seq for 22 patients treated with radiation + immunotherapy
Other
2022-04-17
EGAS00001006213
Somatic L1 retrotranspositions in normal human cells
Other
2022-04-18
EGAS00001006214
scRNA mCRC PDO
Other
2022-04-19
EGAS00001006215
Transcriptomic analysis of peripheral blood dendritic cells and monocytes from patients with familial chilblain lupus and hetereozygous mutations in TREX1
Transcriptome Analysis
2022-04-19
EGAS00001006218
Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19
Other
2022-04-25
EGAS00001006222
MGP Panel: a comprehensive targeted genomics panel for molecular profiling of multiple myeloma patients
Other
2022-04-25
EGAS00001006228
Serum Proteome Profiling Identifies Early Markers of Therapeutic Response to Neoadjuvant Chemotherapy of Breast Cancer
Other
2022-04-25
EGAS00001006229
Biomarker Data from KATHERINE: A Phase III Study of Adjuvant Trastuzumab Emtansine versus Trastuzumab in Patients with Residual Invasive Disease after Neoadjuvant Therapy for HER2-Positive Breast Cancer
Other
2022-04-26
EGAS00001006230
Extensive patient-to-patient single nuclei transcriptome heterogeneity in pheochromocytomas and paragangliomas
Other
2022-04-26
EGAS00001006232
Salivary Gland Cancer TSO500 dataset
Other
2022-04-27
EGAS00001006233
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Other
2022-04-28
EGAS00001006234
Hereditary_Cerebellar_Ataxias___Whole_Genome_Sequencing___2021
Whole Genome Sequencing
2022-04-28
EGAS00001006235
Whole exome sequencing of PMBCL
Other
2022-04-29
EGAS00001006236
glioblastoma single cell RNAseq
Other
2022-04-29
EGAS00001006237
A brain precursor atlas reveals the acquisition of developmental-like states in adult cerebral tumours
Other
2022-04-29
EGAS00001006240
PIAMA nasal RNAseq data
Other
2022-05-01
EGAS00001006242
RNA-sequencing of mechanical stress induced osteoarthritis-like damage in aged human cartilage explants treated with the anti-deiodinase iopanoic acid
Other
2022-05-02
EGAS00001006246
Single-cell RNA-seq data from 3 HGSOC patient-derived organoids and corresponding tumor or ascites
Other
2022-05-02
EGAS00001006247
Genomics characterization of BRAF-V600E colorectal cancer patients treated with anti-BRAF/EGFR
Exome Sequencing
2022-05-02
EGAS00001006249
Molecular characterization of a renal cell carcinoma PDX cohort
Cancer Genomics
2022-05-05
EGAS00001006251
Accumulation of copy number alterations and clinical progression across advanced prostate cancer
Other
2022-05-05
EGAS00001006252
The University of Hong Kong Gastric Cancer Organoids RHO Signaling Study
Other
2022-05-06
EGAS00001006254
Germline sequencing
Other
2022-05-07
EGAS00001006257
The Gut Microbiome of renal transplant recipients – Cross-sectional
Other
2022-05-09
EGAS00001006258
The Gut Microbiome of liver transplant recipients – Cross-sectional + Longitudinal (renal and liver)
Other
2022-05-09
EGAS00001006260
Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes
Other
2022-05-09
EGAS00001006262
Induced pluripotent stem cell lines (iPSC lines) produced from skin and blood cells.
Other
2022-05-11
EGAS00001006263
Single-cell analysis reveals transcriptomic and epigenomic impacts on the maternal-fetal interface upon SARS-CoV-2 infection
Other
2022-05-12
EGAS00001006265
Bulk and single-cell AML RNA-seq post ex vivo culture
Other
2022-05-12
EGAS00001006266
Genetic Determinants of Mannose-binding Lectin Activity Predispose to Thromboembolic Complications in Critical COVID-19
Other
2022-05-12
EGAS00001006267
Transcriptome analysis of samples derived from GBM tumors, and relevant cell lines established and maintained at 5% or 20% oxygen.
Other
2022-05-12
EGAS00001006268
ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution
Cancer Genomics
2022-05-13
EGAS00001006273
RFX6-mediated dysregulation defines human β cell dysfunction in early type 2 diabetes
Transcriptome Analysis
2022-05-14
EGAS00001006275
Characterization of alternative promoter usage in advanced prostate cancer
RNASeq
2022-05-16
EGAS00001006276
Germline variant analysis in childhood AML
Other
2022-05-17
EGAS00001006280
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Other
2022-05-17
EGAS00001006281
COPD and neutrophils
Other
2022-05-17
EGAS00001006282
Evolutionary histories of breast cancer and related clones
Cancer Genomics
2022-05-18
EGAS00001006283
Altered neutrophil and granulopoiesis biology underlie a poor outcome sepsis endotype
Transcriptome Analysis
2022-05-18
EGAS00001006284
COVID-19 GWAS in Japanese
Other
2022-05-19
EGAS00001006285
Deep whole genome sequencing identifies recurrent genomic alterations in breast cancer cell lines and patient derived xenograft models
Other
2022-05-20
EGAS00001006286
Combination of CDK4/6 with BET-bromodomain and PI3K/mTOR inhibitors in medulloblastoma in vitro and in vivo
Other
2022-05-20
EGAS00001006288
Combined – whole blood and skin fibroblasts - transcriptomic analysis in Psoriatic arthritis.
Other
2022-05-21
EGAS00001006289
An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington’s disease patient neurons
Other
2022-05-22
EGAS00001006293
Oncogenic chimeric transcription factors drive tumor-specific transcription, processing, and translation of silent genomic regions
Other
2022-05-23
EGAS00001006294
Whole genome sequencing of multifocal small intestinal neuroendocrine tumors
Whole Genome Sequencing
2022-05-23
EGAS00001006295
Whole exome and genome sequencing investigations of perinatal death
Other
2022-05-24
EGAS00001006298
The immunopeptidome landscape associated with T cell infiltration, inflammation and immune-editing in lung cancer
Other
2022-05-24
EGAS00001006299
RP-1843 Arcagen - Gastrointestinal rare cancers (GI)
Other
2022-05-24
EGAS00001006300
Human Developmental Biology Resource (HDBR) abnormal fetal samples
Other
2022-05-24
EGAS00001006305
Low input capture Hi-C (liCHi-C) identifies promoter-enhancer interactions at high-resolution.
Other
2022-05-24
EGAS00001006306
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Other
2022-05-25
EGAS00001006308
A Risk Score Incorporating Low Pass Whole Genome Sequencing of Cell Free DNA from Patients Receiving CD19 CAR T-Cell Therapy for Large B-Cell Lymphoma
Whole Genome Sequencing
2022-05-26
EGAS00001006309
HNF1A haploinsufficiency causes decreased insulin expression, dysregulation of pancreatic progenitor signature genes and affects chromatin accessibility
RNASeq
2022-05-26
EGAS00001006313
Single cell transcriptomics of hESC-derived midbrain dopaminergic neurons generated by a new human development-based protocol
Other
2022-05-27
EGAS00001006314
Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression
Other
2022-05-27
EGAS00001006317
Shallow nanopore RNA sequencing enables transcriptome profiling for precision cancer medicine (Hipo_021)
Cancer Genomics
2022-05-30
EGAS00001006320
Childhood Cancer Model Atlas
Other
2022-06-01
EGAS00001006321
Fragment ends of circulating microbial DNA as signatures for infectious diseases
Other
2022-06-02
EGAS00001006322
COPD and neutrophils sc
Other
2022-06-03
EGAS00001006323
COPD and neutrophils sc rhapsody
Other
2022-06-05
EGAS00001006327
Detection of early seeding of Richter transformation in chronic lymphocytic leukemia
Other
2022-06-06
EGAS00001006328
Long-read sequencing for cell-free DNA analysis (human)
Other
2022-06-07
EGAS00001006329
Long-read sequencing for cell-free DNA analysis (mouse)
Other
2022-06-07
EGAS00001006330
Spatial multi-omic map of human myocardial infarction
Other
2022-06-07
EGAS00001006331
Intratumoural heterogeneity and immune modulation in lung adenocarcinoma of female smokers and never smokers
Other
2022-06-07
EGAS00001006332
A clinically annotated post-mortem approach to study multi-organ somatic mutational clonality in normal tissues
Exome Sequencing
2022-06-07
EGAS00001006334
Targeting the bicarbonate transporter SLC4A4 overcomes immunosuppression and immunotherapy resistance in pancreatic cancer
Other
2022-06-08
EGAS00001006336
Genomics of drug sensitivity in acute lymphoblastic leukemia
Other
2022-06-09
EGAS00001006339
Platelet RNAseq data for SLFN14 K219N patients
Other
2022-06-10
EGAS00001006340
Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment
Other
2022-06-10
EGAS00001006342
Molecular determinants of outcomes in relapsed mantle cell lymphoma treated with ibrutinib or temsirolimus in the MCL3001 (RAY) trial
Cancer Genomics
2022-06-10
EGAS00001006343
Single cell genomic variation induced by mutational processes in cancer
Other
2022-06-10
EGAS00001006344
Placebo-only arm transcriptomic analysis of the phase 3 PROTECT clinical trial
Other
2022-06-13
EGAS00001006345
Genetic regulation of gene expression in human brain cell types
Other
2022-06-14
EGAS00001006347
Single cell whole genome sequencing of high hyperdiploid acute lymphoblastic leukemia
Other
2022-06-14
EGAS00001006348
The admixture histories of Cabo Verde
Population Genomics
2022-06-14
EGAS00001006350
molecular profiles of serum-derived extracellular vesicles in high-grade serous ovarian cancer
Other
2022-06-14
EGAS00001006351
Rhabdoid tumor sequencing data
Other
2022-06-15
EGAS00001006352
Brain tumor sequencing data
Other
2022-06-15
EGAS00001006353
Diffuse Intrinsic Pontine Glioma
Other
2022-06-15
EGAS00001006354
Acute myeloid leukemia sequencing data
Other
2022-06-15
EGAS00001006355
Glioma sequencing data
Other
2022-06-15
EGAS00001006356
Soft tissue sarcoma sequencing data
Cancer Genomics
2022-06-15
EGAS00001006357
early-Duodenal Cancer sequencing study
Other
2022-06-15
EGAS00001006358
Clonal dominance defines metastatic dissemination in pancreatic cancer
Other
2022-06-15
EGAS00001006362
Juntendo Muscle Study (JMS)
Other
2022-06-17
EGAS00001006363
Muscle SATellite cell study (MSAT)
Other
2022-06-17
EGAS00001006364
Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation.
Cancer Genomics
2022-06-17
EGAS00001006365
Widespread hypertranscription in aggressive human cancers
Other
2022-06-17
EGAS00001006369
RNA-seq analysis of metastatic prostate cancer solid tumor biopsies
Other
2022-06-20
EGAS00001006370
Transcriptome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome
Transcriptome Analysis
2022-06-20
EGAS00001006371
Genome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome
Whole Genome Sequencing
2022-06-20
EGAS00001006372
Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19
Other
2022-06-21
EGAS00001006373
Longitudinal ctDNA in Uveal Melanoma
Other
2022-06-21
EGAS00001006374
Pathogenic variants damage cell compositions and single cell transcription in cardiomyopathies
Other
2022-06-22
EGAS00001006375
An Atlas of Cells in the Human Tonsil
Other
2022-06-22
EGAS00001006376
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Other
2022-06-22
EGAS00001006377
Plasma whole genome sequencing from patients with stage IV colorectal cancer and microsatellite instability
Other
2022-06-22
EGAS00001006378
Whole genome landscape of 25 metastatic cutaneous squamous cell carcinoma cSCC patients
Other
2022-06-23
EGAS00001006380
Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from post-mortem neuropathologically-confirmed control individuals.
Other
2022-06-28
EGAS00001006381
HSP90 inhibitor resistant cell line
Other
2022-06-28
EGAS00001006383
Exome & MiSeq sequencing of individuals with Huntington's disease
Other
2022-06-28
EGAS00001006385
CNV profile in HSP90 inhibitor resistant K562 cells
Other
2022-06-29
EGAS00001006388
Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data
Other
2022-06-30
EGAS00001006392
Single-cell study of 14 childhood medulloblastoma patients
Whole Genome Sequencing
2022-07-01
EGAS00001006393
Homologous recombination deficiency derived from whole-genome sequencing predicts platinum response in triple-negative breast cancers
Other
2022-07-01
EGAS00001006394
Chromatin accessibility changes in hiPSC-derived neurons after BDNF and KCl stimulations
Other
2022-07-01
EGAS00001006395
Quantitative Exploratory Proteomics Analysis of Glioblastoma in Initial and Recurrent Tumors
Other
2022-07-01
EGAS00001006396
CD8+ Tumor-Infiltrating Lymphocyte Abundance is a Positive Prognostic Indicator in Nasopharyngeal Cancer
Other
2022-07-04
EGAS00001006398
Multi-omics analyses of airway host-microbe interactions in chronic obstructive pulmonary disease identify potential therapeutic interventions
Other
2022-07-04
EGAS00001006400
Molecular profiling of EBV associated diffuse large B-cell lymphoma
Other
2022-07-05
EGAS00001006401
Study of the microenvironment of angioimmunoblastic T-cell lymphoma
Cancer Genomics
2022-07-06
EGAS00001006404
Sex chromosome aneuploidies give rise to changes in the circular RNA profile
Other
2022-07-07
EGAS00001006406
DNA methylation-based prognostic subtypes of chordoma tumors in tissue
Other
2022-07-07
EGAS00001006408
Genomic landscape and molecularly-informed therapy in thymic carcinoma and other advanced thymic epithelial tumors (H021, HIPO)
Other
2022-07-08
EGAS00001006410
RNA sequencing data of 142 samples from 142 patients with HER2+ breast cancer treated with letrozole or tamoxifen (SOLTI PAMELA trial)
Other
2022-07-08
EGAS00001006411
Induction Failure in Childhood and Young Adult T-cell Acute Lymphoblastic Leukemia
Cancer Genomics
2022-07-08
EGAS00001006417
INDIA
Other
2022-07-11
EGAS00001006419
Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge
Other
2022-07-12
EGAS00001006420
Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge
Other
2022-07-12
EGAS00001006421
Cystic fibrosis multi-omics study
Other
2022-07-12
EGAS00001006422
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities
Other
2022-07-12
EGAS00001006423
GWAS genotype data of Japanese
Other
2022-07-13
EGAS00001006425
Prostate cancer ancestral genomic disparity
Other
2022-07-13
EGAS00001006427
Dataset with genome-wide array data from 64 Tunisian and 45 Moroccan individuals.
Other
2022-07-13
EGAS00001006428
Palbociclib resistance analyses on breast cancer bone metastasis PDX
Other
2022-07-13
EGAS00001006429
Analyses of IACS-010759 treatment resistance on breast cancer bone metastases
Other
2022-07-13
EGAS00001006431
Whole exome-sequencing of pediatric and adult H3-K27M diffuse midline glioma
Other
2022-07-15
EGAS00001006432
Malignant mesothelioma EWAS on European prospective study
Epigenetics
2022-07-15
EGAS00001006433
ctDNA quantification in Ewing sarcoma patients
Other
2022-07-16
EGAS00001006434
Exploring germline and somatic mutagenesis in the extended family with germline pathogenic variant in POLD1
Other
2022-07-18
EGAS00001006439
Copy Number Variation using Affymetrix Optima Array
Other
2022-07-18
EGAS00001006440
Genetic regulation of RNA splicing in human pancreatic islets
Other
2022-07-18
EGAS00001006441
Transcriptome profiling of three giant cell tumour of bone cell lines
Other
2022-07-19
EGAS00001006442
Time-dependent characterization of CNS response in COVID-19
Other
2022-07-19
EGAS00001006444
Airway Dysbiosis Accelerates Lung Function Decline in Chronic Obstructive Pulmonary Disease
Other
2022-07-19
EGAS00001006445
T cell reactivity of MHC epitopes
Other
2022-07-21
EGAS00001006452
WGS of PMBCL
Cancer Genomics
2022-07-22
EGAS00001006453
Whole-Exome Sequencing analyses in tamoxifen-associated endometrial cancer
Other
2022-07-22
EGAS00001006456
Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population
Other
2022-07-23
EGAS00001006457
Chromatin activation profiling of stereotyped chronic lymphocytic leukemias reveals a subset #8 specific signature
Other
2022-07-25
EGAS00001006459
Case Report: early contribution of germline and nevi genetic alterations to a rapidly-progressing Cutaneous Melanoma Patient
Exome Sequencing
2022-07-25
EGAS00001006460
RaScALL: Rapid screening of RNA-seq in acute lymphoblastic leukaemia
Other
2022-07-26
EGAS00001006461
High-resolution lung adenocarcinoma expression subtypes identify tumors with dependencies on MET, CDK4, CDK6, and PD-L1
Other
2022-07-26
EGAS00001006462
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Other
2022-07-27
EGAS00001006463
in silico drug target prediction for melanoma
Other
2022-07-27
EGAS00001006464
Colorectal cancer transcriptomics with primary and metastatic samples
Other
2022-07-27
EGAS00001006465
Colorectal cancer genomics with primary and metastatic samples
Other
2022-07-27
EGAS00001006466
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Other
2022-07-27
EGAS00001006468
OAC RNASeq
Other
2022-07-28
EGAS00001006469
OAC scRNASeq
Other
2022-07-28
EGAS00001006470
OAC WGS
Other
2022-07-28
EGAS00001006472
Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Other
2022-07-29
EGAS00001006473
Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Other
2022-07-29
EGAS00001006474
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Other
2022-07-29
EGAS00001006477
The HLA ligandome of oropharyngeal squamous cell carcinomas reveals shared tumor-exclusive peptides for semi-personalized vaccination
Other
2022-07-29
EGAS00001006478
Tumor microenvironment study of ovarian granulosa cell tumors
Other
2022-07-29
EGAS00001006479
Comprehensive de novo variant discovery with HiFi long-read sequencing
Other
2022-07-30
EGAS00001006486
Blina_Tumour_project
Whole Genome Sequencing
2022-08-03
EGAS00001006487
Characterization of Arabian Peninsula whole exomes
Other
2022-08-04
EGAS00001006488
SPECIAL: Dissecting the melanoma ecosystem one cell at the time during immunotherapy
Other
2022-08-05
EGAS00001006489
Colorectal cancer study
Other
2022-08-05
EGAS00001006490
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Other
2022-08-05
EGAS00001006491
Control of Focal Adhesion Kinase Activation by RUNX1-regulated miRNAs in high-risk AML
Other
2022-08-06
EGAS00001006492
RNAseq analysis on metastatic Colorectal Cancer xenografts samples
RNASeq
2022-08-08
EGAS00001006494
TRACERx NSCLC - Whole exome multiregion sequencing data
Exome Sequencing
2022-08-09
EGAS00001006495
Upper cortical layer-driven network impairment in schizophrenia
Other
2022-08-09
EGAS00001006497
Bulk RNA-seq of stromal cells from multiple cancer types
Other
2022-08-10
EGAS00001006498
Finding structural variation from the human skin fibroblast at the single-cell level
Other
2022-08-10
EGAS00001006499
The Extracellular RNA Quality Control (exRNAQC) study (phase 2)
RNASeq
2022-08-11
EGAS00001006502
Immune microenvironment and lineage tracing help deciphering Rosette-forming GlioNeuronal Tumors: a multi-omic analysis of 9 cases
Other
2022-08-12
EGAS00001006503
Histone modifications of cfDNA
Epigenetics
2022-08-15
EGAS00001006510
Reliable assessment of telomere maintenance mechanisms in neuroblastoma
Other
2022-08-17
EGAS00001006511
ATAC-Seq on OCIAML-22 Fractions
Other
2022-08-17
EGAS00001006512
RNA-Seq on OCIAML-22 Fractions
Other
2022-08-17
EGAS00001006513
Whole Genome Sequencing on OCIAML-22
Other
2022-08-17
EGAS00001006517
Multi-region RNA sequencing of tumour regions and tumour-adjacent normal lung tissue
Other
2022-08-19
EGAS00001006518
Gene signature for predicting homologous recombination deficiency in triple-negative breast cancer
Other
2022-08-19
EGAS00001006519
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Other
2022-08-22
EGAS00001006520
ATAC-seq/ChIP part
Other
2022-08-22
EGAS00001006521
RNA-seq SE
Other
2022-08-22
EGAS00001006522
RNA-seq PE
Other
2022-08-22
EGAS00001006523
RRBS data from TRACERx non-small cell lung cancer (NSCLC) tumours and matched normal adjacent tissue.
Other
2022-08-22
EGAS00001006526
Paired WGS data from Wilms Tumors
Other
2022-08-23
EGAS00001006527
Characterization of Leukemic Stem Cells in DNMT3Amut and NPM1mut AMLs
Other
2022-08-23
EGAS00001006528
Renal Cell Carcinoma Tumors From S-TRAC trial (NCT00375674) Whole Transcriptome Sequencing
Other
2022-08-23
EGAS00001006529
Renal Cell Carcinoma Tumors From S-TRAC trial (NCT00375674) Exome Sequencing
Other
2022-08-23
EGAS00001006530
Complex patterns of genomic heterogeneity identified in 42 tumor samples and ctDNA of a pulmonary atypical carcinoid patient
Cancer Genomics
2022-08-23
EGAS00001006531
Bulk RNA data from Wilms Tumors
Other
2022-08-24
EGAS00001006532
Somatic Inactivation of Breast Cancer Predisposition Genes in Tumours Associated with Pathogenic Germline Variants
Other
2022-08-24
EGAS00001006533
Neuroblastoma Evolution
Other
2022-08-24
EGAS00001006534
Single-cell RNA-seq of human kidney tumors
Other
2022-08-25
EGAS00001006535
Characterizing the tumor immune microenvironment of ependymomas using targeted gene expression profiles and RNA-sequencing the pros and cons
Other
2022-08-25
EGAS00001006537
single nuclei RNASeq of 5 regions of the human prenatal brain
Other
2022-08-25
EGAS00001006538
Single-cell multi-omics of relapse/refractory multiple myeloma patients (Hipo K08K/H067/K43R)
Other
2022-08-26
EGAS00001006539
cfDNA in Hereditary And High-Risk Malignancies (CHARM)
Other
2022-08-26
EGAS00001006540
Robust methylation-based classification of brain tumours using nanopore sequencing
Other
2022-08-28
EGAS00001006542
Significant and pervasive effects of RNA degradation on Nanopore direct RNA sequencing
Other
2022-08-29
EGAS00001006545
Duplexseq_of_the_interstrand_crosslinks_WGS
Other
2022-08-30
EGAS00001006547
A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain)
Other
2022-08-30
EGAS00001006551
Adult human kidney organoids originate from CD24+ cells and represent an advanced model for adult polycystic kidney disease
Other
2022-08-31
EGAS00001006552
Synthetic genotypes and phenotypes of 500.000 individuals
Other
2022-09-01
EGAS00001006553
Integrative modeling of tumor genomes and epigenomes for enhanced cancer diagnosis by cell-free DNA.
Other
2022-09-01
EGAS00001006554
A living biobank of patient-derived ductal carcinoma in situ Mouse-INtraDuctal xenografts identifies factors associated with risk of invasive progression
Other
2022-09-02
EGAS00001006555
Ovarian carcinosarcoma genomics and eribulin response
Other
2022-09-05
EGAS00001006557
Sequencing Data of HGSC patient-derived cell lines and organoids
Cancer Genomics
2022-09-05
EGAS00001006558
H3Africa - Kidney Disease Research Network
Other
2022-09-05
EGAS00001006559
Single-cell ATAC-seq analysis for COVID19 patients
Other
2022-09-05
EGAS00001006560
Single-cell RNA-seq analysis for COVID19 patients
Other
2022-09-05
EGAS00001006563
Single cell transcriptome profiling of childhood soft tissue sarcomas
Other
2022-09-05
EGAS00001006565
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Other
2022-09-05
EGAS00001006567
Deciphering somatic mosaic structural variation in human blood lineages using single-cell multiomics
Other
2022-09-06
EGAS00001006572
HSC_colony_many_years_post_allogeneic_bone_marrow_transplant___Bait_set_3
Other
2022-09-06
EGAS00001006573
Longitudinal monitoring of cell-free DNA methylation in ALK-positive non-small cell lung cancer patients
Other
2022-09-06
EGAS00001006574
Erasmus MC COVID-19 cohort-associated connected datasets study
Other
2022-09-06
EGAS00001006575
Whole-genome sequencing in gastric cancer (part2)
Other
2022-09-07
EGAS00001006576
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Other
2022-09-07
EGAS00001006577
The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21
Other
2022-09-07
EGAS00001006582
Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models: validation cohort
Other
2022-09-08
EGAS00001006583
RNAseq of liver harvested from CDAHFD mice treated for 8 weeks with either the MGAT2 inhibitor compound BMS-963272 or vehicle
Other
2022-09-08
EGAS00001006584
RNAseq of jejunum (small intestine) harvested from CDAHFD mice treated for 8 weeks with either the MGAT2 inhibitor compound BMS-963272 or vehicle
Other
2022-09-08
EGAS00001006585
Somatic mutations predict an aggressive phenotype in meningioma but do not drive grade progression
Other
2022-09-09
EGAS00001006591
Real-time analysis of the cancer genome and fragmentome from plasma and urine short and long cell-free DNA using Nanopore sequencing
Other
2022-09-09
EGAS00001006593
Whole-Transcriptomic Profiling of Sorted Human Renal Cell Carcinoma Immune Populations
Other
2022-09-09
EGAS00001006594
RNA sequencing of AD, MCI and control ONS cells
RNASeq
2022-09-12
EGAS00001006595
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates
Other
2022-09-12
EGAS00001006596
Transcriptomic profiles of chronic lymphocytic leukemia before and after frontline therapy: 5-year results from the randomized CLL14 study
Other
2022-09-13
EGAS00001006598
Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Other
2022-09-14
EGAS00001006599
Defective homologous recombination in HCC
Other
2022-09-14
EGAS00001006600
Genomic landscape of DS-ALL
Cancer Genomics
2022-09-14
EGAS00001006601
Cetuximab treatment of metastasis-derived organoids (LMO)
RNASeq
2022-09-15
EGAS00001006602
HLF COPD Transcriptomics
Other
2022-09-15
EGAS00001006603
HLF COPD DNA Methylomics
Epigenetics
2022-09-15
EGAS00001006604
Hi-C analysis of metastatic prostate tumors
Other
2022-09-15
EGAS00001006605
DNA and RNA sequencing data from Ovarian Carcinosarcoma patients from the Glasgow Cohort.
Other
2022-09-15
EGAS00001006609
Long-read sequencing for cell-free DNA analysis (human pacbio)
Other
2022-09-19
EGAS00001006610
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - WGS data
Other
2022-09-19
EGAS00001006612
Hi-C analysis of metastatic prostate tumors - Part 2
Other
2022-09-19
EGAS00001006613
Tumorigenic role of Musashi-2 in aggressive mantle cell lymphoma
Other
2022-09-20
EGAS00001006617
microRNA and isomiR profiling of Stage 1 epithelial ovarian carcinoma
Other
2022-09-21
EGAS00001006621
Genetic characterization patients affected by Cancer of Unknown Primary
Other
2022-09-22
EGAS00001006629
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures (Hipo_021)
Other
2022-09-23
EGAS00001006631
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Other
2022-09-26
EGAS00001006632
Nasal epithelial cells of PCD and non-PCD patients grown at air-liquid interface for RNAseq analysis
Other
2022-09-27
EGAS00001006633
Identification of neoantigen from MSI-CRC patient derived organoids and its application for targeting by autologous T cells
Other
2022-09-27
EGAS00001006642
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - Cancer Panel data
Other
2022-09-28
EGAS00001006643
Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome
Other
2022-09-28
EGAS00001006644
Multi-organ landscape of therapy-resistant melanoma
Other
2022-09-29
EGAS00001006645
H3Africa - Trauma And Neurobiology: Maternal stress and transgenerational impact. Search for Epigenetic Markers
Other
2022-09-29
EGAS00001006646
Follicular Lymphoma Whole Genome and Transcriptome Sequencing
Cancer Genomics
2022-09-29
EGAS00001006648
Integrative pan-cancer genomic and transcriptomic analyses of refractory metastatic cancer
Other
2022-09-30
EGAS00001006649
UCSF WCDT WGS/WGBS mCRPC
Other
2022-09-30
EGAS00001006651
Germline sequencing
Other
2022-10-02
EGAS00001006652
Intratumoral Heterogeneity and Clonal Evolution Induced by HPV Integration.
Other
2022-10-02
EGAS00001006653
Whole genome analysis of pediatric patients with medulloblastoma
Other
2022-10-03
EGAS00001006656
Exome sequencing from cfDNA blood samples. 159 samples at 2x101bp Illumina reads in Fastq format.
Other
2022-10-03
EGAS00001006657
Nasal brushes analysis
Other
2022-10-03
EGAS00001006659
Gene copy number variation in pediatric mental illness in a general population
Other
2022-10-03
EGAS00001006660
Persistent Mutation Burden Drives Sustained Anti-Tumor Immune Responses
Other
2022-10-03
EGAS00001006661
scRNA-seq of patient-derived PDAC organoids and matched CAFs
Other
2022-10-03
EGAS00001006663
BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Other
2022-10-04
EGAS00001006665
single-cell RNA-Seq of colorectal cancer patient samples
Transcriptome Analysis
2022-10-05
EGAS00001006666
bulk RNA-Seq of colorectal cancer patient samples
RNASeq
2022-10-05
EGAS00001006670
DNA methylation landscape of prostate cancer
Other
2022-10-07
EGAS00001006674
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Other
2022-10-10
EGAS00001006675
T cell responses of ALS patients
Other
2022-10-10
EGAS00001006678
Longitudinal evaluation of serum microRNAs as biomarkers for neuroblastoma burden and therapeutic p53 reactivation
Other
2022-10-10
EGAS00001006679
Identification of genomic aberrations in low-grade serous ovarian cancer
Other
2022-10-10
EGAS00001006680
Advanced molecular neuropathology to increase diagnostic accuracy in pediatric neurooncology
Other
2022-10-12
EGAS00001006688
Tocilizumab treatment leads to early resolution of myeloid dysfunction and lymphopenia in patients hospitalized with COVID-19
Other
2022-10-13
EGAS00001006689
Genomic and ecologic characteristics of the airway microbial-mucosal complex
Other
2022-10-13
EGAS00001006690
RNA seq before and after cold pressor test
Other
2022-10-13
EGAS00001006692
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Other
2022-10-13
EGAS00001006693
Whole Genome Sequences of 18th century African descended individuals from Charleston, South Carolina.
Other
2022-10-13
EGAS00001006694
Single-cell atlas of multiple myeloma and precursor diseases
Other
2022-10-14
EGAS00001006695
Tissue DNA, WBC DNA and cfDNA (deep-)sequencing of mCRC patients treated with doublet chemotherapy and anti-EGFR in the CAIRO5 study
Other
2022-10-17
EGAS00001006696
Shallow sequencing of organoid/xenograft or human colorectal metastases
Whole Genome Sequencing
2022-10-17
EGAS00001006697
Targeted Sequencing Xenturion
Exome Sequencing
2022-10-17
EGAS00001006698
Characterization of chromatin accessibility in metastatic prostate cancer
Other
2022-10-17
EGAS00001006700
Plasma DNA end analysis (mouse)
Other
2022-10-18
EGAS00001006701
Cell-free DNA cleavages analysis (human)
Other
2022-10-18
EGAS00001006702
Characterization of MCSP+ melanoma DCC and MelDCC lines
Other
2022-10-19
EGAS00001006703
High-resolution testing of ctDNA dynamics predicts survival in metastatic NSCLC
Other
2022-10-20
EGAS00001006704
Whole blood transcriptomic analysis of ANCA-associated vasculitis
Other
2022-10-20
EGAS00001006705
Germline sequencing
Other
2022-10-20
EGAS00001006706
Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification (H021)
Other
2022-10-21
EGAS00001006707
The University of Hong Kong Colon Cancer GCV Study
Other
2022-10-21
EGAS00001006710
Genomic profiling of subcutaneous patient derived xenograft models of solid childhood cancer
Cancer Genomics
2022-10-21
EGAS00001006711
Hexanucleotide repeat expansions in C9orf72 alter microglial responses and prevent a coordinated glial reaction in ALS
Other
2022-10-22
EGAS00001006712
DNA methylation-based classification of sinonasal tumors [Proteomics data]
Other
2022-10-23
EGAS00001006713
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Other
2022-10-23
EGAS00001006716
A single-cell transcriptional gradient in human cutaneous memory T cells restricts Th17/Tc17 identity
Other
2022-10-26
EGAS00001006718
Test Study for EGA using data from 1000 Genomes Project - Big CRAM, BAM, VCF and BCF files used for testing
Other
2022-10-28
EGAS00001006719
Whole genome sequencing of AVM endothelial and non-endothelial cell fractions
Other
2022-10-28
EGAS00001006720
Sputum fungal microbiota in an overall healthy population in Guangdong province, China
Other
2022-10-29
EGAS00001006721
Sputum bacterial microbiota in an overall healthy population in Guangdong province, China
Other
2022-10-29
EGAS00001006723
Deconvolution of bulk RNA-Seq using single cell RNA-Seq
Other
2022-10-31
EGAS00001006724
Comprehensive Whole-Genome Sequence Annotation to Resolve the Genetic Architecture of Cerebral Palsy
Whole Genome Sequencing
2022-11-01
EGAS00001006725
Whole genome sequencing dataset of 200 trio families from the CHILD cohort study.
Whole Genome Sequencing
2022-11-01
EGAS00001006727
Bulk RNAseq of mCRC organoids
Other
2022-11-02
EGAS00001006728
Single cell RNA-sequencing of tissues from NSCLC patients treated with chemoimmunotherapy
Transcriptome Analysis
2022-11-02
EGAS00001006729
Targeted sequencing of brain AVM tissues
Other
2022-11-02
EGAS00001006730
Measurement of SARS-CoV-2 variants fraction in infected alveolar cells
Other
2022-11-03
EGAS00001006731
WGS of CD138+ samples collected from MM patients
Other
2022-11-03
EGAS00001006732
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Other
2022-11-03
EGAS00001006736
NIBIT-M4 Clinical Trial samples
Other
2022-11-04
EGAS00001006739
Neoadjuvant Chemo or Combined Chemo-Radiation Therapy of Pancreatic Ductal Adenocarcinoma Yields Fundamentally Different Proteome Biology of the Residual Tumor Mass
Other
2022-11-07
EGAS00001006744
Structural Expression of BMMF in tissues of colorectal, lung and pancreatic cancer patients
Other
2022-11-08
EGAS00001006746
Human primary and metastatic colorectal cancer (CRC) samples
RNASeq
2022-11-09
EGAS00001006747
Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling (hipo_021)
Other
2022-11-09
EGAS00001006755
Human pan-cancer plasma cfRNA study - raw data
Other
2022-11-10
EGAS00001006757
Enrichment of oral-derived bacteria in inflamed colorectal tumors and distinct associations of Fusobacterium in the mesenchymal subtype
Other
2022-11-11
EGAS00001006758
The Iberian Roma genetic variant server
Other
2022-11-11
EGAS00001006759
Neutrophil extracellular traps have auto-catabolic activity and produce mononucleosome-associated circulating DNA
Whole Genome Sequencing
2022-11-13
EGAS00001006762
Single-cell transcriptomics identifies pathogenic T-helper 17.1 cells and pro-inflammatory monocytes in ICI-related pneumonitis
Other
2022-11-14
EGAS00001006767
Data containing genome-wide SNP data from Northwestern Amazonia
Other
2022-11-14
EGAS00001006769
BCR-ABL is enriched in S- and G2-cell cycle phases
Other
2022-11-14
EGAS00001006772
S3 Swedish schizophrenia case-control study
Population Genomics
2022-11-15
EGAS00001006775
Whole Genome Sequencing Data of High Grade Serous Ovarian Cancer
Other
2022-11-16
EGAS00001006778
Multi-omics identify falling LRRC15 as a COVID-19 severity marker and persistent pro-thrombotic signals in convalescence
Other
2022-11-17
EGAS00001006779
Host pathogen interaction long read transcriptome
Other
2022-11-17
EGAS00001006780
Single-cell RNA and ATAC sequencing data analysis of human postmenopausal fallopian tube and ovary
Other
2022-11-17
EGAS00001006781
Tertiary lymphoid structure signatures are associated with immune checkpoint inhibitor related acute interstitial nephritis
Transcriptome Analysis
2022-11-17
EGAS00001006782
PDAC organoid genomic heterogeneity
Other
2022-11-20
EGAS00001006784
Leukemia sequencing study
Other
2022-11-21
EGAS00001006785
Integrative analysis of exome-seq, RNA-seq, ATAC-seq (bulk and single-cell), and Hi-C data generated from 3-D spatially mapped samples acquired during surgical resection from 10 patients diagnosed with IDH-WT glioblastoma
Other
2022-11-21
EGAS00001006786
Frequencies of variants in the Danish population
Whole Genome Sequencing
2022-11-22
EGAS00001006787
scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects
Other
2022-11-22
EGAS00001006788
Transcriptional_reprogramming_from_innate_immune_functions_to_a_pro_thrombotic_signature_upon_SARS_CoV_2_sensing_by_monocytes_in_COVID_19
Transcriptome Analysis
2022-11-22
EGAS00001006789
The molecular landscape of homologous recombination deficient, end-stage, high grade serous ovarian cancer
Other
2022-11-23
EGAS00001006791
DNA methylation atlas of normal human cell types
Other
2022-11-23
EGAS00001006793
Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype
Other
2022-11-23
EGAS00001006794
RNA-sequencing of ex vivo exhausted human antigen-specific T cells
Other
2022-11-23
EGAS00001006796
The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21
Other
2022-11-24
EGAS00001006800
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS
Exome Sequencing
2022-11-28
EGAS00001006801
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS derived
Other
2022-11-28
EGAS00001006802
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq
RNASeq
2022-11-28
EGAS00001006803
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq derived
RNASeq
2022-11-28
EGAS00001006805
Highly sensitive liquid biopsy Duplex sequencing complements tissue biopsy to enhance detection of clinically relevant genetic variants
Other
2022-11-29
EGAS00001006807
Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in HGSOC
Other
2022-11-29
EGAS00001006808
Loss of LGR4/GPR48 causes severe neonatal salt-wasting due to disrupted WNT signaling altering adrenal zonation
Other
2022-11-29
EGAS00001006811
Study of Korean Parkinson's disease
Other
2022-11-30
EGAS00001006813
FFPE, buffycoat and cell free DNA from N. German esophagus cancer patients - 2021
Other
2022-11-30
EGAS00001006818
The impact of BNT162b2 mRNA vaccine against SARS-CoV-2 on adaptive and innate immune responses
Other
2022-11-30
EGAS00001006819
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Other
2022-11-30
EGAS00001006820
NPY methylated ctDNA is a promising biomarker for treatment response monitoring in metastatic colorectal cancer
Cancer Genomics
2022-11-30
EGAS00001006821
Tumor educated platelets for BrCA
RNASeq
2022-12-01
EGAS00001006823
Profiling of childhood neuroblastoma and the immune microenvironment by single-cell sequencing of RNA and TCR
Other
2022-12-01
EGAS00001006826
Epigenome-wide association study of cocaine use disorder in postmortem human brain tissue
Other
2022-12-01
EGAS00001006831
Dynamics of sequence and structural cell-free DNA landscapes in small-cell lung cancer
Other
2022-12-01
EGAS00001006832
The role of MALT1 in driving IBN resistance in MCL
Other
2022-12-01
EGAS00001006833
Malignant progression of an ancestral bone marrow clone harboring a CIC-NUTM2A fusion in isolated myeloid sarcoma
Other
2022-12-02
EGAS00001006836
Single cell RNA sequencing of bone marrow mononuclear cells
Other
2022-12-02
EGAS00001006838
Influence of Genomic Landscape on Cancer Immunotherapy for Newly Diagnosed Ovarian Cancer: Biomarker Analyses from the IMagyn050 Randomized Clinical Trial
Other
2022-12-02
EGAS00001006843
TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - WGS
Cancer Genomics
2022-12-06
EGAS00001006844
TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - RNAseq
Other
2022-12-06
EGAS00001006845
The genome-wide mutational consequences of DNA hypomethylation
Whole Genome Sequencing
2022-12-06
EGAS00001006847
scRNASeq of human innate lymphoid cells from different compartments
Other
2022-12-06
EGAS00001006848
cfDNA dataset from extracelular vesicles and paired non-fractionated samples
Other
2022-12-06
EGAS00001006851
Multiregion Whole Exome and Smart-Seq3 single cell RNA sequencing of Breast Tumors
Other
2022-12-06
EGAS00001006855
Analyzing the expression profiles of genes in ureters with and without indwelling stents using RNAseq
Other
2022-12-06
EGAS00001006856
Early on-treatment changes in circulating tumor DNA fraction and response to enzalutamide or abiraterone in metastatic castration-resistant prostate cancer
Other
2022-12-07
EGAS00001006857
Rifaximin stimulates nitrogen detoxification by PXR-independent mechanisms in human small intestinal organoids
Other
2022-12-07
EGAS00001006860
Exome sequencing of HCV+ lymphoma
Other
2022-12-07
EGAS00001006864
T cell landscape definition by multi-omics identifies galectin-9 as novel immunotherapy target in chronic lymphocytic leukemia (CLL)
Other
2022-12-08
EGAS00001006865
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Other
2022-12-09
EGAS00001006866
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Other
2022-12-09
EGAS00001006868
Smart-seq3 scRNA-seq of cells from primary (OV2295) and metastatic (OV2295R2) high-grade serous ovarian cancer cell-line
Other
2022-12-12
EGAS00001006870
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Other
2022-12-13
EGAS00001006871
RNAseq of paired primary and locally recurrent IDHwt GBM
Other
2022-12-14
EGAS00001006873
Targeted DNA sequencing on 37 Merkel Cell Carcinomas from New Zealand with known Merkel cell polyomavirus status
Other
2022-12-14
EGAS00001006874
WGS of MAPKi acquired resistant samples from patients and PDX models
Other
2022-12-15
EGAS00001006879
Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin
Other
2022-12-15
EGAS00001006881
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Other
2022-12-16
EGAS00001006883
ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy
Other
2022-12-16
EGAS00001006884
Molecular evolution of classic Hodgkin lymphoma revealed through whole genome sequencing of Hodgkin and Reed Sternberg cells
Other
2022-12-19
EGAS00001006885
Transcriptomic analysis of liver CD8+ T cells
Other
2022-12-19
EGAS00001006886
One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Other
2022-12-20
EGAS00001006887
Chronic lymphocytic leukemia IGHV somatic hypermutation detection by targeted capture next-generation sequencing
Other
2022-12-20
EGAS00001006894
Tracing early predictors of glioma evolution under therapy
Other
2022-12-22
EGAS00001006898
Non-viral precision T cell receptor replacement for personalized cell therapy
Other
2022-12-22
EGAS00001006902
PD-L1 blockade in combination with carboplatin as immune induction in metastatic lobular breast cancer: the GELATO-trial
Other
2022-12-24
EGAS00001006903
Tracking the evolution of Therapy-Related Myeloid Neoplasms using chemotherapy signatures
Other
2022-12-26
EGAS00001006904
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Other
2023-01-03
EGAS00001006905
Mechanism of action and resistance to Trastuzumab Deruxtecan in patients with metastatic breast cancer: the DAISY trial
Exome Sequencing
2023-01-04
EGAS00001006906
Genetic landscape of ENKTCL
Cancer Genomics
2023-01-04
EGAS00001006907
germline variants in children with hematological cancer
Other
2023-01-04
EGAS00001006908
IACS treatment on breast cancer bone metastases
Other
2023-01-05
EGAS00001006909
Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection
Other
2023-01-06
EGAS00001006910
Whole Exome and RNA sequencing of synchronous female bilateral breast cancers
Cancer Genomics
2023-01-06
EGAS00001006911
The genomic diversity of Taiwanese Austronesian groups: implications for the ‘Into and Out of Taiwan’ models
Population Genomics
2023-01-06
EGAS00001006913
Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Other
2023-01-09
EGAS00001006914
transcriptome analysis of NK cells sorted from PBMCs at baseline and after addition of a T cell dependent bispecific antibody (TDB)
RNASeq
2023-01-09
EGAS00001006916
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Other
2023-01-10
EGAS00001006919
Genomic and epigenomic study of Japanese renal cell carcinoma including WGS, RNA-seq, ATAC-seq, and methyl-seq
Other
2023-01-12
EGAS00001006920
van Hijfte GBM dataset 2022/A (single-nucleus RNA-seq)
Other
2023-01-12
EGAS00001006923
Tracking early lung cancer metastatic dissemination in TRACERx using ctDNA
Other
2023-01-13
EGAS00001006926
Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1).
Other
2023-01-16
EGAS00001006927
Genomic profiling of localized (lFL) and systemic follicular lymphoma (sFL) reveals novel insights into FL pathogenesis
Other
2023-01-17
EGAS00001006928
Identifying rare genetic variants in 21 highly multiplex autism families
Whole Genome Sequencing
2023-01-17
EGAS00001006929
CYP2C19 long-read sequencing
Other
2023-01-17
EGAS00001006932
Multiome_HB
Other
2023-01-17
EGAS00001006934
Isala Citizen Science Project: Cross-sectional branch
Other
2023-01-17
EGAS00001006935
Bolleboom-Gao peri-tumoral snRNA-seq glioblastoma dataset 2022/A
Other
2023-01-17
EGAS00001006937
TNBC ctDNA Targeted Panel
Other
2023-01-18
EGAS00001006939
Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions(H021/INF)
Other
2023-01-19
EGAS00001006942
Clonal architecture and genomic features of smoking versus non-smoking oncogene-driven East-Asian non-small cell lung cancer
Other
2023-01-20
EGAS00001006944
Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.'
Other
2023-01-20
EGAS00001006945
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Other
2023-01-20
EGAS00001006946
Genomic Analysis of a Metastatic Fusion-negative Embryonal Rhabdomyosarcoma
Cancer Genomics
2023-01-20
EGAS00001006947
Case Report: Rare IKZF1 gene fusions identified in neonate with congenital KMT2A-rearranged Acute Lymphoblastic Leukemia
Other
2023-01-22
EGAS00001006949
Pre-diagnostic saliva microbiota of Finnish children with autoimmune diseases
Other
2023-01-23
EGAS00001006950
Genotype data of Japanese
Other
2023-01-24
EGAS00001006951
Lung Adenocarcinoma Promotion by Air Pollutants
Other
2023-01-24
EGAS00001006952
The immunological characterization of expanded tumor-infiltrating lymphocytes in renal cell carcinoma patients
Other
2023-01-24
EGAS00001006954
Single-cell sequencing of adipose-derived mesenchymal stromal cells and dermal fibroblasts
Transcriptome Analysis
2023-01-25
EGAS00001006958
The multifaceted genomic history of Ashaninka from Amazonian Peru
Other
2023-01-26
EGAS00001006959
PELICAN45 RNAseq Dataset
Other
2023-01-27
EGAS00001006960
The effector program of human CD8 T cells can promote both target cell killing and tissue remodeling
Transcriptome Analysis
2023-01-28
EGAS00001006962
Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epithelium
Other
2023-01-31
EGAS00001006963
GCparagon: Evaluation and correction of GC biases in cell-free DNA at the fragment level
Other
2023-02-01
EGAS00001006964
A novel Patient-Derived 3D Model Recapitulates Mantle Cell Lymphoma Lymph Node Signaling, Immune Profile and in vivo Ibrutinib Responses
Other
2023-02-01
EGAS00001006965
Chronic lymphocytic leukemia patient-derived xenografts recapitulate clonal evolution to Richter transformation
Other
2023-02-01
EGAS00001006966
RNA-seq on bronchial brushings collected in controlled human exposure to diesel exhaust
Other
2023-02-01
EGAS00001006967
Personalized Onco-Genomic Project for pediatric and adolescent patients in British Columbia
Other
2023-02-01
EGAS00001006968
Longitudinal peripheral blood DNA methylation profiling of endoscopic response to tofacitinib in moderate-to-severe ulcerative colitis patients
Epigenetics
2023-02-02
EGAS00001006970
Single-cell RNA-seq and spatial transcriptomics data for the sarcoidosis baseline project
Other
2023-02-02
EGAS00001006973
Treated and control Patient Derived Xenografts of colorectal cancer (CRC) samples
RNASeq
2023-02-02
EGAS00001006975
A capture-based next-generation sequencing panel for the molecular characterization of chronic lymphocytic leukemia
Cancer Genomics
2023-02-02
EGAS00001006976
B Cell Receptor Study From Metastatic Breast Cancer Tumour Samples
Other
2023-02-02
EGAS00001006977
NanoString nCounter® PanCancer IO 360™on anti-PD1/anti-PD1+CTLA4 in patients with metastatic melanoma
Other
2023-02-03
EGAS00001006978
Exome_sequencing_of_UK_Birth_Cohorts___Born_in_Bradford
Other
2023-02-06
EGAS00001006980
scRNA-seq of total bone marrow mononuclear cells and CD3+ T cells of multiple myeloma patients and healthy donors
Other
2023-02-06
EGAS00001006981
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Other
2023-02-06
EGAS00001006982
Diet driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome
Other
2023-02-06
EGAS00001006983
Study of complex rearrangements and mutational signatures in neuroblastoma heterogeneous risk groups.
Other
2023-02-07
EGAS00001006984
RNA sequencing of CCO- and CCO+ human hepatocytes
Other
2023-02-07
EGAS00001006988
Multiomic Sequencing of Paired Primary and Metastatic Small Bowel Carcinoids
Other
2023-02-08
EGAS00001006989
Pharmacogenomic profiling reveals molecular features of chemotherapy resistance in IDH wild type primary glioblastoma
Other
2023-02-08
EGAS00001006990
A single cell view on host immune transcriptional response to in vivo BCG-induced trained immunity
Transcriptome Analysis
2023-02-08
EGAS00001006992
Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Other
2023-02-09
EGAS00001006994
Single cell multi-omic study of H3-K27M mutant diffuse midline glioma across age and location
Other
2023-02-09
EGAS00001006995
Germline variants in childhood cutaneous melanoma
Exome Sequencing
2023-02-10
EGAS00001006999
PhIP-Seq LLD
Other
2023-02-13
EGAS00001007001
Biomarker Screen for Efficacy of Oncolytic Virotherapy in Patient-derived Pancreatic Cancer Cultures
Other
2023-02-14
EGAS00001007002
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Other
2023-02-15
EGAS00001007003
Relevance of TMPRSS2, CD163/CD206 and CD33 in clinical severity stratification of COVID-19
Other
2023-02-15
EGAS00001007004
CAGEKID: Cancer Genomics of the Kidney - Targeted Sequencing
Other
2023-02-15
EGAS00001007006
A machine learning classifier for DNA repair defects using plasma DNA
Cancer Genomics
2023-02-15
EGAS00001007008
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis
Epigenetics
2023-02-16
EGAS00001007011
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Other
2023-02-17
EGAS00001007013
NEC
Other
2023-02-17
EGAS00001007014
Whole genome, RNA-seq and single-cell Multiome profile of multiple myeloma
Cancer Genomics
2023-02-20
EGAS00001007016
Neuroblastoma heterogeneity
Other
2023-02-20
EGAS00001007019
Neuroblastoma heterogeneity
Other
2023-02-21
EGAS00001007021
Single-cell dissection of the immune response after a myocardial infarction
Transcriptome Analysis
2023-02-21
EGAS00001007022
Covid19 RNAseq Fastq files
Other
2023-02-21
EGAS00001007023
Integrated single cell analysis in transformed follicular lymphoma
Other
2023-02-21
EGAS00001007024
RNAseq analysis on metastasis-derived organoids (LMO)
RNASeq
2023-02-22
EGAS00001007025
Shot-gun stool metagenomics and colorectal cancer risk.
Other
2023-02-22
EGAS00001007026
Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells
Cancer Genomics
2023-02-22
EGAS00001007027
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Other
2023-02-23
EGAS00001007029
A novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer
Other
2023-02-24
EGAS00001007033
A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE
Other
2023-02-24
EGAS00001007035
Single cell epigenomic study of H3-K27M mutant diffuse midline glioma across age and location
Other
2023-02-24
EGAS00001007036
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Other
2023-02-24
EGAS00001007038
An IL-1β driven neutrophil-stromal cell axis fosters a BAFF-rich microenvironment in multiple myeloma
Other
2023-02-26
EGAS00001007039
Molecular features of adenomas predicting metachronous colorectal cancer: a nested-case control study
Other
2023-02-27
EGAS00001007041
IMI-RHAPSODY data
Other
2023-02-27
EGAS00001007042
Methylation-based classification of human mesenchymal chondrosarcoma
Other
2023-02-27
EGAS00001007044
Single-cell RNA-seq of cervix and placenta
Other
2023-02-27
EGAS00001007045
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Other
2023-02-28
EGAS00001007047
VRK3 depletion in Pontine Diffuse Midline Glioma (DMG)-K27 altered cells
RNASeq
2023-03-01
EGAS00001007048
Covid19 WGS BAM files
Other
2023-03-01
EGAS00001007049
Genome-wide DNA Copy Number Analysis of high hyperdiploid acute lymphoblastic leukemia
Cancer Genomics
2023-03-01
EGAS00001007050
Covid19 RNAseq BAM files
Other
2023-03-01
EGAS00001007051
RNAseq analysis on primary sites Colorectal Cancer xenografts (PRX) samples
RNASeq
2023-03-02
EGAS00001007052
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Other
2023-03-02
EGAS00001007053
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Other
2023-03-02
EGAS00001007054
PhIP-Seq data
Other
2023-03-03
EGAS00001007055
Single cell RNA-seq from AD and PS patients
Other
2023-03-06
EGAS00001007057
Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Other
2023-03-06
EGAS00001007059
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Other
2023-03-08
EGAS00001007060
RNA sequencing data of 257 samples from 106 patients with HR+/HER2- breast cancer treated with AC plus paclitaxel or letrozole plus ribociclib (SOLTI-1402 CORALLEEN trial)
Other
2023-03-08
EGAS00001007061
Germline whole genome sequencing of patients with Li-Fraumeni syndrome
Other
2023-03-08
EGAS00001007064
Linked-read based analysis of Medulloblastomas
Other
2023-03-10
EGAS00001007066
Genomic determinants of therapy response in ETV6-RUNX1 leukemia
Whole Genome Sequencing
2023-03-10
EGAS00001007067
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Other
2023-03-11
EGAS00001007070
RNA-seq of PDAC patient-derived xenograft tumors
Transcriptome Analysis
2023-03-13
EGAS00001007071
cfDNAme allows early prediction of PE
Other
2023-03-13
EGAS00001007072
LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patients
Cancer Genomics
2023-03-13
EGAS00001007075
DNA methylation of peripheral blood leukocytes from patients with Li-Fraumeni syndrome
Other
2023-03-13
EGAS00001007076
Treatment stratification and biomarker validation using patient-derived head and neck cancer organoids
Other
2023-03-14
EGAS00001007077
ACT-Discover: identifying karyotype heterogeneity in pancreatic cancer evolution using ctDNA
Other
2023-03-14
EGAS00001007078
Clonally resolved single-cell multi-omics identifies routes of cellular differentiation in acute myeloid leukemia
Other
2023-03-14
EGAS00001007079
Transgenerational transmission of reproductive and metabolic dysfunction in the male progeny of polycystic ovary syndrome
Other
2023-03-14
EGAS00001007080
Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Other
2023-03-14
EGAS00001007081
PEACE melanoma 14
Other
2023-03-15
EGAS00001007082
Covid19 WGS Variant analysis
Whole Genome Sequencing
2023-03-15
EGAS00001007083
Spatial transcriptomics reveal topological immune landscapes of Asian head and neck angiosarcoma
Other
2023-03-16
EGAS00001007084
sWGS of Pap test smears from healthy donors and HGSOC patients and matched tumor tissue
Other
2023-03-17
EGAS00001007085
Papua New Guinean Genome Altitude Project
Population Genomics
2023-03-17
EGAS00001007086
The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer
Other
2023-03-17
EGAS00001007087
Evolutionary landscape of clonal hematopoiesis in 3359 individuals from the general population
Other
2023-03-17
EGAS00001007088
Nasal Polyp RNAsequencing, Skaraborg Sweden
Other
2023-03-18
EGAS00001007089
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis using bronchial specimens
Other
2023-03-18
EGAS00001007090
Point-of-care monitoring of head and neck cancer treatment response and recurrence development using nanopore-based ctDNA consensus sequencing
Forensic or Paleo-genomics
2023-03-19
EGAS00001007091
Cell-to-cell variability in Myc dynamics drives transcriptional heterogeneity in cancer cells
Other
2023-03-20
EGAS00001007092
Multiple Myeloma follow-up sequencing study
Other
2023-03-20
EGAS00001007093
Long-term organoid culture of a small intestinal neuroendocrine tumor
Other
2023-03-21
EGAS00001007094
Epigenetic landscape of mixed phenotype leukemias
Other
2023-03-21
EGAS00001007095
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Other
2023-03-21
EGAS00001007097
Gene expression profiles in paediatric ETV6-RUNX1 leukemia
RNASeq
2023-03-21
EGAS00001007099
Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Other
2023-03-21
EGAS00001007101
Cancer sequencing for somatic variant calling
Other
2023-03-22
EGAS00001007103
Genomic profiling of Rare Tumors
Other
2023-03-22
EGAS00001007104
Whole Exome Sequencing data of six chRCC tumors corresponding to three patients
Other
2023-03-22
EGAS00001007105
Genomic Landscape of Follicular Lymphoma Across a Wide Spectrum of Clinical Behaviors
Cancer Genomics
2023-03-22
EGAS00001007106
Covid19 WGS Raw Read files
Other
2023-03-22
EGAS00001007108
Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq
Other
2023-03-23
EGAS00001007110
Single-cell and bulk RNA-sequencing of nivolumab-treated glioblastoma
Other
2023-03-23
EGAS00001007111
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Other
2023-03-23
EGAS00001007112
RNA stability controlled by m6A methylation contributes to X-to-autosome dosage compensation in mammals
Other
2023-03-23
EGAS00001007113
TIGIT is the central player in T-cell suppression associated with CAR T-cell relapse in mantle cell lymphoma
RNASeq
2023-03-23
EGAS00001007115
Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Other
2023-03-27
EGAS00001007116
Covid19 Transcriptomic Data analysis in Irish Population
Other
2023-03-27
EGAS00001007117
Identification of Long Non-coding RNA Biomarker of Human Lupus Nephritis Disease Activity
Other
2023-03-27
EGAS00001007118
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetes
Other
2023-03-27
EGAS00001007119
RNA sequencing of a glioblastoma PDX cohort
Other
2023-03-27
EGAS00001007120
Paired diagnostic and relapse medulloblastoma sequencing
Other
2023-03-27
EGAS00001007124
RNA-Seq on GeparSixto tissue samples
Other
2023-03-28
EGAS00001007125
T-cell receptor sequencing of tumor-infiltrating lymphocytes (TIL) in breast cancer
Other
2023-03-28
EGAS00001007126
GM adipose tissue study
Other
2023-03-29
EGAS00001007127
Human lymphoma plasma cfRNA - raw data
Other
2023-03-30
EGAS00001007131
Archaeogenomic distinctiveness of the Isthmo-Colombian area
Forensic or Paleo-genomics
2023-03-31
EGAS00001007136
T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Other
2023-03-31
EGAS00001007143
Persister cell phenotypes contribute to poor patient outcomes after neoadjuvant chemotherapy in PDAC (Hipo_015)
Cancer Genomics
2023-04-03
EGAS00001007144
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Other
2023-04-03
EGAS00001007145
The Sys4MS cohort: a prospective cohort of patients with Multiple Sclerosis and omics
Other
2023-04-03
EGAS00001007146
Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Other
2023-04-04
EGAS00001007156
Cachexia - Non-Cachexia Metagenome Analysis
Other
2023-04-07
EGAS00001007157
Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes
Epigenetics
2023-04-08
EGAS00001007159
Evaluation of triple negative breast cancer with heterogeneous immune infiltration
Other
2023-04-11
EGAS00001007160
Exploring high-throughput drug sensitivity testing in neuroblastoma cell lines and patient-derived tumor organoids in the era of precision medicine
Other
2023-04-12
EGAS00001007161
Neuroblastoma tumors by bulk RNAseq, from Berlanga et al, 2022
Other
2023-04-12
EGAS00001007162
A GWAS of Progression in Multiple Sclerosis
Other
2023-04-12
EGAS00001007163
Oesophageal_Adenocarcinoma_Organoid_PacBio
Cancer Genomics
2023-04-13
EGAS00001007164
Spatial and temporal intra-tumoural heterogeneity in advanced High-Grade Serous Ovarian Cancer: implications for surgical and clinical outcomes
Other
2023-04-13
EGAS00001007165
RNAseq
Other
2023-04-13
EGAS00001007166
ATACseq
Other
2023-04-13
EGAS00001007167
Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia
Other
2023-04-13
EGAS00001007171
A Machine Learning Tool Integrating Circulating Cell-Free DNA Methylation with Clinical Variables for Non-Invasive Diagnosis of Liver Graft Pathology
Other
2023-04-17
EGAS00001007172
Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma
Other
2023-04-18
EGAS00001007173
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Other
2023-04-18
EGAS00001007180
Chip_seq_oesophageal_adenocarcinoma_
Cancer Genomics
2023-04-18
EGAS00001007184
Accuracy and repeatability of epigenome-based signatures trained on Illumina MethylationEPIC BeadChip data
Epigenetics
2023-04-18
EGAS00001007186
Structural variant analysis of homologous recombination-deficient genomes
Other
2023-04-20
EGAS00001007189
HGSOC organoid sequencing study
Cancer Genomics
2023-04-20
EGAS00001007192
Enhanced detection of MRD with cfDNA Fragmentomics.
Cancer Genomics
2023-04-23
EGAS00001007194
Human liver NPCs single cell project
Other
2023-04-23
EGAS00001007195
Developing somatic copy number and mutation calling tools for a bespoke sequencing platform
Other
2023-04-24
EGAS00001007197
Monocyte Spike-in RNASeq
Other
2023-04-24
EGAS00001007200
The genetic history of the southern Andes from present-day Mapuche ancestry
Other
2023-04-26
EGAS00001007201
Methylation profiles in patients with blastic plasmacytoid dendritic cell neoplasm
Other
2023-04-27
EGAS00001007204
Bacterial SNPs in the human gut microbiome associate with host BMI
Other
2023-05-04
EGAS00001007205
RNA-Sequencing data of patient derived normal fibroblasts (NFs), cancer associated fibroblasts (CAFs) and tumor spheroid samples
Other
2023-05-04
EGAS00001007210
Clinical Activity of Combined Telomerase Vaccination and Pembrolizumab in Advanced Melanoma: Results from a Phase I Trial
Other
2023-05-05
EGAS00001007211
WGS
Other
2023-05-06
EGAS00001007212
RNAseq
Other
2023-05-06
EGAS00001007213
deep-learning-powered tissue deconvolution for cfDNA
Other
2023-05-07
EGAS00001007216
TB-DAR Genotyping Study
Other
2023-05-08
EGAS00001007217
Transcriptome analyses of a large cohort of adult B cell acute lymphoblastic leukemia samples
Transcriptome Analysis
2023-05-08
EGAS00001007219
Digital tEchnology For Lung Cancer Treatment
Other
2023-05-09
EGAS00001007221
RNAseq of Soft Tissue Sarcomas
Other
2023-05-09
EGAS00001007222
Integrated genetic analysis of primary CNS lymphoma
Cancer Genomics
2023-05-10
EGAS00001007223
Whole exome sequencing (WES) of previously untreated AML samples
Other
2023-05-10
EGAS00001007227
Analysis of circulating miRNAs for the identification of new prognostic and predictive markers in gastro-entero-pancreatic neuroendocrine tumour (GEP-NET)
RNASeq
2023-05-10
EGAS00001007229
A transcriptomic approach to understand patient susceptibility to pneumonia after abdominal surgery
Other
2023-05-10
EGAS00001007230
Multiomic profiling of pleomorphic rhabdomyosarcoma
Other
2023-05-10
EGAS00001007231
WGS of KCNQ2 R201C patient derived iPSC and its isogenic line
Whole Genome Sequencing
2023-05-11
EGAS00001007235
Dataset with genome-wide array data from Algerian Amazigh (Chaoui and Mozabite) and non-Amazigh individuals
Other
2023-05-14
EGAS00001007236
Whole-Exome Sequences from Imazighen and non-Imazghen from Algeria
Other
2023-05-14
EGAS00001007237
Analysis of a cohort of familial ademomatous polyposis patients bearing APC gene mutation
Other
2023-05-15
EGAS00001007238
cfDNA dataset from the urine supernatant of ovarian cancer patients and healthy controls
Other
2023-05-15
EGAS00001007239
Genetic scoring guide for personalized risk assessment in pediatric B-cell precursor Acute Lymphoblastic Leukemia
Other
2023-05-15
EGAS00001007240
Enhancer plasticity in endometrial tumorigenesis demarcates non-coding driver mutations and alterations in 3D genome organization to boost oncogene expression
Other
2023-05-15
EGAS00001007241
Proteomic predictors of individualized nutrient-specific insulin secretion in health and disease
Transcriptome Analysis
2023-05-15
EGAS00001007242
Single-cell decoding of drug induced transcriptomic reprogramming in triple negative breast cancers
Other
2023-05-16
EGAS00001007244
Genomic analyses to identify metabolic vulnerabilities
Other
2023-05-16
EGAS00001007245
Pre-existing immunity drives the response to neoadjuvant chemotherapy in esophageal adenocarcinoma
Other
2023-05-16
EGAS00001007248
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Other
2023-05-16
EGAS00001007249
Whole genome sequencing of patients with or at risk for HCC
Other
2023-05-16
EGAS00001007250
H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa
Other
2023-05-17
EGAS00001007253
Clonal_selection_after_gene_therapy_in_SCD___Duplex_sequencing
Cancer Genomics
2023-05-18
EGAS00001007254
Transcriptomics identifies blunted immunomodulatory effects of vitamin D in people with multiple sclerosis
Other
2023-05-19
EGAS00001007255
Colon adenomas and adenocarcinomas and matched mucosae
Other
2023-05-19
EGAS00001007257
Methylome profiling of epithelioid sarcoma
Other
2023-05-20
EGAS00001007259
An isogenic human iPSC model unravels neurodevelopmental abnormalities in SMA
Other
2023-05-22
EGAS00001007261
Spatial tumor microenvironment characterization and outcome of relapsed/refractory classic Hodgkin lymphoma
Other
2023-05-23
EGAS00001007262
Gene expression of neutrophils in response to Mtb infection in persons living with HIV
RNASeq
2023-05-23
EGAS00001007263
Cardiovascular disease biomarkers derived from circulating cell-free DNA methylation
Other
2023-05-23
EGAS00001007286
Multi-omic analysis of the tumor microenvironment shows clinical correlations in Ph1 study of atezolizumab +/- SoC in MM
Other
2023-05-26
EGAS00001007288
Comprehensive single-cell genome analysis at nucleotide resolution using the PTA Analysis Toolbox
Other
2023-05-26
EGAS00001007290
Proteomic Analysis of Non-Muscle Invasive and Muscle Invasive Bladder Cancer Highlights Distinct Subgroups With Metabolic, Matrisomal, and Immune Hallmarks
Other
2023-05-26
EGAS00001007291
Elucidating the heterogeneity of immunotherapy response and immune-related toxicities by longitudinal ctDNA and immune cell compartment tracking in lung cancer
Cancer Genomics
2023-05-26
EGAS00001007292
The genomic landscape of recurrent ovarian high grade serous carcinoma: the BriTROC-1 study
Other
2023-05-27
EGAS00001007295
Exploration of neuroblastoma xenograft models for tumor extracellular RNA profiling in murine blood plasma
RNASeq
2023-05-30
EGAS00001007296
Human data for chromatin accessibility (ATAC-Seq and scATAC-Seq) and transcriptome (RNA-Seq and scRNA-Seq) in eight B-cell precursors, from HSC to Naive B cells
Other
2023-05-30
EGAS00001007297
Clinical outcomes and immune correlates of response to nivolumab plus chemoradiotherapy in women with locally-advanced cervical cancer – NiCOL study
Other
2023-05-30
EGAS00001007298
Early ctDNA molecular response captures therapeutic response in the first stage of CCTG BR.36 ctDNA-directed, multi-center phase II study of molecular response adaptive immunotherapy in non-small cell lung cancer
Cancer Genomics
2023-05-30
EGAS00001007299
Circulating tumor DNA, pathological and immunologic responses to neoadjuvant nivolumab or nivolumab plus relatlimab and chemoradiotherapy in resectable esophageal/gastroesophageal junction cancer
Cancer Genomics
2023-05-30
EGAS00001007300
RNAseq of Colorectal cancer organoid-stroma biobank cohort
Other
2023-05-30
EGAS00001007301
WES of Colorectal cancer organoid-stroma biobank cohort
Other
2023-05-30
EGAS00001007302
Baseline RNAseq analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67
RNASeq
2023-05-31
EGAS00001007303
Targeted exome DNA sequencing analysis of POETIC Good/Poor Responders to aromatase inhibitors based on change in Ki67
Exome Sequencing
2023-05-31
EGAS00001007305
Healthy human B-lymphopoiesis RNA-Seq reference using FACS sorted bone marrow aspirates
RNASeq
2023-05-31
EGAS00001007306
Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring
Other
2023-05-31
EGAS00001007307
Human subsistence and signatures of selection on chemosensory genes
Population Genomics
2023-06-01
EGAS00001007308
Cell-free DNA sequencing data of healthy control, atrophic gastritis, and gastric cancer patients’ blood
Cancer Genomics
2023-06-02
EGAS00001007309
Therapeutic vulnerabilities in CCA from different etiologies identified using integrative multi-omics enhancer activity profiling
Epigenetics
2023-06-03
EGAS00001007310
GWAS on covid-19 severity and susceptibility in the province of Bergamo, Italy
Other
2023-06-05
EGAS00001007313
ExHiBITT shows that microbiome from colon biopsies, caecal fluid from colonoscopies and faecal samples shape different microbiome-host interactions
Other
2023-06-06
EGAS00001007314
Investigation of different library preparation and tissue of origin deconvolution methods for urine and plasma cfDNA methylome analysis
Other
2023-06-06
EGAS00001007321
Possible DNA damage after paternal exposure to ionizing radiation in radar technicians
Other
2023-06-07
EGAS00001007323
A longitudinal single-cell atlas of treatment response in pediatric AML
Other
2023-06-07
EGAS00001007324
Analysis of Loose Ends in Cancer Genome Structure
Other
2023-06-07
EGAS00001007327
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Other
2023-06-08
EGAS00001007330
DECONVOLUTION OF HEMATOPOIETIC STEM/PROGENITOR CELL SIGNALING IN HUMAN AML
Other
2023-06-09
EGAS00001007331
H3Africa - Stroke Investigative Research and Education Networks
Other
2023-06-09
EGAS00001007332
Bone marrow single cell genomics from blood cancer samples
Other
2023-06-09
EGAS00001007333
Detection of somatic mutations of angioimmunoblastic T-cell lymphoma
Exome Sequencing
2023-06-11
EGAS00001007334
Facial Skin Biophysical Multi-Parameter and Microbiome-Based Korean Skin Cutoype (KSC) Determination
Other
2023-06-12
EGAS00001007335
FGFR-driven urothelial cancer
Cancer Genomics
2023-06-12
EGAS00001007336
Breast cancer sequencing data
Transcriptome Analysis
2023-06-12
EGAS00001007337
Tonsil Sequencing dataset
RNASeq
2023-06-12
EGAS00001007339
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
Other
2023-06-12
EGAS00001007343
ATAC-Seq of healthy and IBD blood samples
Other
2023-06-12
EGAS00001007344
ATAC-Seq of inflamed and non-inflamed biopsies
Other
2023-06-12
EGAS00001007345
ATAC-Seq of CD4 T cell subsets
Other
2023-06-12
EGAS00001007346
Modulation of the peripheral blood immune cell transcriptome by vitamin D3 supplementation in people with a first demyelinating event: a randomized placebo-controlled trial
Other
2023-06-14
EGAS00001007349
Organoid_Derivation_Project___GRCh38___TGS
Other
2023-06-16
EGAS00001007350
A circulating biomarker for severity of facioscapulohumeral muscular dystrophy
Other
2023-06-19
EGAS00001007351
Assessing mitochondrial bioenergetics in coronary artery disease: A translational left ventricular tissue study in humans (The AMBITION study).
Other
2023-06-19
EGAS00001007355
The genomic landscape of GCs
Other
2023-06-19
EGAS00001007358
Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging
Other
2023-06-20
EGAS00001007362
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Other
2023-06-22
EGAS00001007363
Towards standardized whole exome sequencing (WES) for cancer patients: lessons from a multicentric pilot study
Other
2023-06-22
EGAS00001007364
WES sequencing of TRACERx NSCLC patient-derived xenograft models
Other
2023-06-22
EGAS00001007365
Serial TERT rearrangement breakpoint quantification in circulating tumor DNA enables minimal residual disease monitoring in patients with neuroblastoma
Other
2023-06-22
EGAS00001007367
bulk TCR-seq data IMCISION
Other
2023-06-23
EGAS00001007368
scRNA-seq and scTCR-seq data IMCISION
Other
2023-06-23
EGAS00001007369
Cellular composition of spheres derived from lymph nodes of lung cancer patients
Other
2023-06-23
EGAS00001007370
Sclerosing Epithelioid Fibrosarcoma sequencing data
Other
2023-06-23
EGAS00001007372
Mechanism of action and resistance to Trastuzumab Deruxtecan in patients with metastatic breast cancer
Exome Sequencing
2023-06-24
EGAS00001007373
High-resolution, patient-level dissection of IL-23 blockade in cutaneous psoriasis
Other
2023-06-25
EGAS00001007374
Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution
Other
2023-06-26
EGAS00001007375
Analysis of the Elements Involved in the Enrichment of a Panel of Genomic Regions by Nanopore Sequencing Using Adaptive Sampling
Other
2023-06-26
EGAS00001007379
Multi-region sequencing of PDAC patients
Exome Sequencing
2023-06-26
EGAS00001007381
SNP array ARID1B patients
Other
2023-06-27
EGAS00001007383
Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
Other
2023-06-27
EGAS00001007385
Atypical B cells and impaired SARS-CoV-2 neutralisation following heterologous vaccination in the elderly
Other
2023-06-28
EGAS00001007386
AT2 COPD Methylomics
Other
2023-06-28
EGAS00001007387
AT2 COPD Transcriptomics
Other
2023-06-28
EGAS00001007389
Targeting TRIP13 in Wilms Tumor with Nuclear Export Inhibitors
Other
2023-06-28
EGAS00001007390
Single cell landscape of Multicentric Castleman Disease in monozygotic twins
Whole Genome Sequencing
2023-06-29
EGAS00001007393
Efficacy of nivolumab in pediatric cancers with high mutation burden and mismatch-repair deficiency
Other
2023-06-30
EGAS00001007396
Evaluation of somatic mutations in urine samples as a non-invasive method for the detection and molecular classification of endometrial cancer
Other
2023-07-03
EGAS00001007397
scRNAsequencing of in vitro expanded limbal stem cells of aniridia donors
Other
2023-07-04
EGAS00001007398
Total RNA sequencing from the TNT trial (NCT00532727)
Other
2023-07-04
EGAS00001007399
shallow WGS and deep targeted panel on ctDNA in rhabdomyosarcomas
Other
2023-07-04
EGAS00001007400
Genome-wide cell-free DNA biological patterns in patients with cancer
Other
2023-07-04
EGAS00001007402
Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths
Cancer Genomics
2023-07-05
EGAS00001007403
checup
Other
2023-07-06
EGAS00001007404
Genomic and immune signatures predict clinical outcome in newly diagnosed multiple myeloma treated with immunotherapy regimens
Cancer Genomics
2023-07-06
EGAS00001007405
Cohesin Mutations in AML
Other
2023-07-06
EGAS00001007409
Diagnosis of multisystem inflammatory syndrome in children by a whole-blood transcriptional signature
Other
2023-07-06
EGAS00001007411
Analysis of enhancer-promoter connectivity alterations
Other
2023-07-07
EGAS00001007412
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types
Other
2023-07-09
EGAS00001007421
Prognostic markers of DNA methylation and NGS sequencing in progressive glioblastoma from the EORTC-26101 trial
Other
2023-07-13
EGAS00001007426
Translation of non-canonical open reading frames as a cancer cell survival mechanism in childhood medulloblastoma
Other
2023-07-13
EGAS00001007427
Single-cell proteogenomics of MDS upon AZA
Other
2023-07-13
EGAS00001007428
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types (RNAseq)
Other
2023-07-13
EGAS00001007430
Patient-derived organoids identify tailored therapeutic options and determinants of plasticity in sarcomatoid urothelial bladder cancer
Cancer Genomics
2023-07-13
EGAS00001007432
Regenerative effects of MSC treatment on busulfan-induced small intestine damaged organoids.
Other
2023-07-14
EGAS00001007438
Intra-prostatic tumour evolution, steps in metastatic spread and histogenomic associations revealed by integration of multi-region whole genome sequencing with histopathological features
Other
2023-07-17
EGAS00001007445
CUPiD, a cfDNA methylation-based tissue-of-origin classifier for Cancers of Unknown Primary
Cancer Genomics
2023-07-17
EGAS00001007449
Methylome study on human spermatogenic cells
Epigenetics
2023-07-19
EGAS00001007450
RSV infection of primary bronchial epithelial cells in asthma
Other
2023-07-20
EGAS00001007451
Machine Learning Signal Enrichment for Ultrasensitive Plasma Tumor Burden Monitoring
Other
2023-07-20
EGAS00001007453
Whole_Genome_Sequencing_OMELib__Cord_blood_
Other
2023-07-21
EGAS00001007454
RNA_Seq_OMELib__Cord_blood_
Other
2023-07-21
EGAS00001007458
Whole Genome sequencing of Angolan and Mozambican individuals
Other
2023-07-24
EGAS00001007465
BCL3-rearrangements in B-cell lymphoid neoplasms occur in two breakpoint clusters associated with different diseases
Cancer Genomics
2023-07-25
EGAS00001007466
Effective reprogramming of patient-derived M2-polarized glioblastoma-associated microglia/macrophages by treatment with GW2580
Other
2023-07-26
EGAS00001007467
AML FLT3 TCR study
Other
2023-07-27
EGAS00001007472
scATAC-seq and combined scRNA-seq of the human first trimester neurodevelopment
Epigenetics
2023-08-03
EGAS00001007474
Epithelioid haemangioendothelioma (EHE) case series from the Stafford Fox Rare Cancer Program
Other
2023-08-04
EGAS00001007475
Ultra-fast deep-learned pediatric CNS tumor classification.
Other
2023-08-04
EGAS00001007477
Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations
Cancer Genomics
2023-08-08
EGAS00001007479
DLBCLR
Other
2023-08-08
EGAS00001007481
Oncoprint GSCCs
Other
2023-08-09
EGAS00001007482
Single-cell profiling of co-cultures of GSCCs and macrophages
Other
2023-08-09
EGAS00001007484
Discrepancies in Tumour Mutation Burden (TMB) reporting from sequential Endobronchial ultrasound trans bronchial needle aspiration (EBUS TBNA) samples within single lymph node stations
Other
2023-08-10
EGAS00001007486
Subclonal somatic copy number alterations emerge and dominate in recurrent osteosarcoma
Other
2023-08-10
EGAS00001007487
Optimizing single-cell transcriptomic discrimination of atopic dermatitis versus psoriasis vulgaris
Other
2023-08-10
EGAS00001007488
Single cell transcriptomics of human adrenal gland reveal chromosomal alterations in adrenocortical cells
Other
2023-08-11
EGAS00001007493
Methylation-based deconvolution of cell-free DNA
Epigenetics
2023-08-14
EGAS00001007499
The genomic echoes of the last Green Sahara on the Fulani and Sahelian people
Whole Genome Sequencing
2023-08-16
EGAS00001007501
Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer
Other
2023-08-17
EGAS00001007507
Whole genome sequencing of 108 epileptic patients from CENet cohort
Other
2023-08-18
EGAS00001007508
ExomeSeq Neoantigen Immunogenicity Landscapes
Other
2023-08-18
EGAS00001007509
RNASeq Neoantigen Immunogenicity Landscape
Other
2023-08-18
EGAS00001007510
Immune landscape of oncohistone-mutant gliomas reveals diverse myeloid populations and tumor-promoting behavior
Other
2023-08-18
EGAS00001007513
Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation
Other
2023-08-22
EGAS00001007519
AfricanNeo aDNA Study
Other
2023-08-22
EGAS00001007521
FFPE WGS for optimizing mutation signature extraction from archival HGSC samples
Other
2023-08-22
EGAS00001007525
Integrative genomic analyses of European intrahepatic cholangiocarcinoma: new ROS1 fusion gene and PBX1 as prognostic marker
Cancer Genomics
2023-08-24
EGAS00001007528
RNA sequencing of control OM cells exposed to traffic-related air pollutants
RNASeq
2023-08-28
EGAS00001007529
RAGE engagement by SARS-CoV-2 enables monocyte infection and underlies COVID-19 severity
RNASeq
2023-08-28
EGAS00001007530
Mevalonate Metabolism fuels pro-inflammatory function of Vd2 T cells
RNASeq
2023-08-28
EGAS00001007532
Peripheral blood DNA methylation of Crohn's disease patients starting treatment with either vedolizumab of ustekinumab
Other
2023-08-28
EGAS00001007534
RNA sequencing on intestinal biopsies from inflammatory bowel disease patients treated with vehicle control, MEK inhibitor, or infliximab
Other
2023-08-29
EGAS00001007539
CTD-ILD_BALF_and_blood_scRNA-seq_data
Transcriptome Analysis
2023-08-30
EGAS00001007542
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants
Other
2023-08-30
EGAS00001007545
Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring
Other
2023-08-31
EGAS00001007546
GLASS-NL DNA-Methylation
Epigenetics
2023-08-31
EGAS00001007547
Study of PD-1 negative CD8 effector T-cells in advanced HCC with single-cell sequencing
Other
2023-08-31
EGAS00001007550
Effects of busulfan, fludarabine and clofarabine treatment on human small intestinal organoids generated from healthy donors
Other
2023-09-01
EGAS00001007552
RNA sequencing in primary inflammatory (TPP) macrophages treated with a MEK1/2 inhibitor
Other
2023-09-01
EGAS00001007553
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Other
2023-09-01
EGAS00001007555
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Other
2023-09-01
EGAS00001007556
Lower respiratory tract single cell and neutrophil extracellular trap profiling of COVID-19-associated pulmonary aspergillosis
Transcriptome Analysis
2023-09-01
EGAS00001007560
Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages
Epigenetics
2023-09-04
EGAS00001007561
Sequential Antigen-loss and Branching Evolution in Lymphoma after Anti-CD19 and Anti-CD20 Targeted T Cell Engaging Immunotherapy
Other
2023-09-04
EGAS00001007562
H3K27ac ChIP-seq in primary inflammatory (TPP) macrophages
Other
2023-09-04
EGAS00001007563
Immune and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 trials
Other
2023-09-06
EGAS00001007565
Complex structural variation patterns in pediatric solid tumors
Other
2023-09-07
EGAS00001007571
CS Baby Biome
Metagenomics
2023-09-11
EGAS00001007573
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Other
2023-09-11
EGAS00001007574
Idiosyncratic and generic single nuclei and spatial transcriptional patterns in papillary and anaplastic thyroid cancers
Other
2023-09-11
EGAS00001007575
Structural and Non-Coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases
Whole Genome Sequencing
2023-09-13
EGAS00001007577
CDK4 phosphorylation status and rational use for combining CDK4/6 and BRAF/MEK inhibition in advanced thyroid carcinomas
Other
2023-09-14
EGAS00001007578
Peripheral blood DNA methylome in adalimumab-treated patients with rheumatoid arthritis
Other
2023-09-17
EGAS00001007580
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups
Other
2023-09-18
EGAS00001007584
Germline variants in patients diagnosed with both uveal and cutaneous melanoma
Other
2023-09-22
EGAS00001007585
Exploring the cell-free total RNA transcriptome in diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma patients as biomarker source in blood plasma liquid biopsies
Other
2023-09-25
EGAS00001007590
SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Other
2023-10-02
EGAS00001007593
Low-coverage whole-genome sequencing of cancer and healthy plasma circulating DNA
Cancer Genomics
2023-10-03
EGAS00001007601
PRADO trial - Personalized response-directed surgery and adjuvant therapy after neoadjuvant ipilimumab plus nivolumab in stage III melanoma
Other
2023-10-11
EGAS00001007606
Somatic mutations associate with clonal expansion of CD8+ T cells
Transcriptome Analysis
2023-10-12
EGAS00001007611
A clinically applicable connectivity signature for glioblastoma includes the tumor network driver CHI3L1
Other
2023-10-20
EGAS00001007618
RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines
Cancer Genomics
2023-10-25
EGAS00001007628
DERMATLAS__Leiomyosarcoma_WES
Cancer Genomics
2023-10-31
EGAS00001007629
DERMATLAS__Leiomyoma_WES
Cancer Genomics
2023-10-31
EGAS00001007630
DERMATLAS__Leiomyoma_RNAseq
Cancer Genomics
2023-10-31
EGAS00001007631
DERMATLAS__Leiomyosarcoma_RNAseq
Cancer Genomics
2023-10-31
EGAS00001007650
Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Other
2023-11-21
EGAS00001007658
Buccal Sample Methylation for Breast Cancer Detection
Other
2023-12-01
EGAS00001007660
Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with Constitutional Mismatch Repair Deficiency
Other
2023-12-05
EGAS00001007661
Targeted and shallow whole genome sequencing identifies therapeutic opportunities in p53abn endometrial cancers
Other
2023-12-05
EGAS00001007666
DNA-methylation variability in normal mucosa of patients with adenomatous polyps: a marker of field cancerization
Epigenetics
2023-12-08
EGAS00001007703
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Other
2024-01-31
EGAS00001007705
DERMATLAS__Poroma_WES
Other
2024-02-01
EGAS00001007710
Nala GSI GSAv3 PGx Study
Other
2024-02-05
EGAS00001007717
noninvasive lung cancer subtyping
Other
2024-02-15
EGAS00001007742
Isoform-level profiling of m6A modifications in human brain
Other
2024-03-04
EGAS00001007744
RNA isoform repertoire of neuropsychiatric risk genes in human brain
Other
2024-03-05
EGAS00001007745
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Other
2024-03-07
EGAS00001007746
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Other
2024-03-07
EGAS00001007753
NEOPREDICT-Lung: Neoadjuvant Immunotherapy for Resectable NSCLC
Other
2024-03-19
EGAS00001007764
PREGO reference panel - 3234 individuals from Western France. Individuals' birthplaces are available in epsg.io/2154 (RGF93 v1 / Lambert-93 -- France) coordinates.
Other
2024-03-27
EGAS00001007766
Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression
Other
2024-03-27
EGAS00001007767
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Other
2024-04-02
EGAS00001007773
Repli-seq data for 'Replication timing alterations are associated with mutation acquisition during tumour evolution in breast and lung cancer'
Other
2024-04-09
EGAS00001007783
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Epigenetics
2024-04-17
EGAS00001007786
Genomic_Advances_in_Sepsis__GAinS__genotyping
Other
2024-04-22
EGAS00001007789
Exome_sequencing_of_UK_Birth_Cohorts___Millennium_Cohort_Study
Other
2024-04-25
EGAS00001007803
To_profile_the_landscape_of_sebaceous_tumours___RNA
Other
2024-05-13
EGAS00001007816
Genetic Effects on the Skin Methylome in Healthy Older Twins
Epigenetics
2024-05-15
EGAS00001007818
This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs)
Other
2024-05-16
EGAS00001007831
Measuring the Efficiency of Purging by Nonrandom Mating in Human Populations
Population Genomics
2024-05-29
EGAS00001007840
Tyrol Lifestyle Atlas: Intermittent Fasting Methylation Data
Other
2024-06-13
EGAS00001007844
Array-based methylation analysis of SDHB-deficient pheochromocytoma and paraganglioma
Cancer Genomics
2024-06-14
EGAS00001007852
Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read Sequencing
Other
2024-06-19
EGAS00001007854
XClone for analyzing somatic copy number alterations
Other
2024-06-25
EGAS00001007877
Metabolic profiling of patient-derived organoids reveals nucleotide synthesis as a metabolic vulnerability in malignant rhabdoid tumors
Other
2024-07-23
EGAS50000000038
Submission 3 - study_title 1
Synthetic Genomics
2023-03-14
EGAS50000000039
Submission 3 - study_title 2
Metagenomics
2023-03-14
EGAS50000000042
Submission 15 - study_title 1
Metagenomics
2023-03-22
EGAS50000000043
Submission 15 - study_title 2
RNASeq
2023-03-22
EGAS50000000046
test
RNASeq
2023-03-23
EGAS50000000047
My title
Whole Genome Sequencing
2023-03-21
EGAS50000000049
Test 1
Synthetic Genomics
2023-04-17
EGAS50000000050
GA4GH Connect study
Whole Genome Sequencing
2023-04-19
EGAS50000000051
human genome reference hg19 (b37)
Whole Genome Sequencing
2023-04-19
EGAS50000000055
Submission 40 - study_title 1
Exome Sequencing
2023-05-11
EGAS50000000056
Submission 40 - study_title 2
Exome Sequencing
2023-05-11
EGAS50000000078
Submission 13 - study_title 1
Exome Sequencing
2023-05-19
EGAS50000000080
Submission 14 - study_title 1
Cancer Genomics
2023-05-19
EGAS50000000081
Submission 14 - study_title 2
Transcriptome Sequencing
2023-05-19
EGAS50000000082
Submission 15 - study_title 1
Population Genomics
2023-05-19
EGAS50000000083
Submission 15 - study_title 2
Exome Sequencing
2023-05-19
EGAS50000000084
Submission 64 - study_title 1
Exome Sequencing
2023-05-23
EGAS50000000085
Submission 64 - study_title 2
Whole Genome Sequencing
2023-05-23
EGAS50000000086
Submission 19 - study_title 1
Metagenomics
2023-05-23
EGAS50000000087
Submission 19 - study_title 2
Metagenomics
2023-05-23
EGAS50000000090
SYNTHETIC DATA: Study of hearing loss
Synthetic Genomics
2023-05-23
EGAS50000000103
Submission 70 - study_title 1
Pooled Clone Sequencing
2023-05-26
EGAS50000000104
Submission 70 - study_title 2
Transcriptome Sequencing
2023-05-26
EGAS50000000107
Submission 72 - study_title 1
Forensic or Paleo-genomics
2023-05-26
EGAS50000000108
Submission 72 - study_title 2
Resequencing
2023-05-26
EGAS50000000111
SYNTHETIC DATA: Study with test data from 1000 Genome Project
Synthetic Genomics
2023-05-29
EGAS50000000116
Submission 27 - study_title 1
Forensic or Paleo-genomics
2023-05-30
EGAS50000000117
Submission 27 - study_title 2
RNASeq
2023-05-30
EGAS50000000118
Submission 80 - study_title 1
Cancer Genomics
2023-05-30
EGAS50000000119
Submission 80 - study_title 2
Whole Genome Sequencing
2023-05-30
EGAS50000000120
Submission 84 - study_title 1
Epigenetics
2023-06-07
EGAS50000000121
Submission 84 - study_title 2
RNASeq
2023-06-07
EGAS50000000122
FAKE STUDY: Clinical Evaluation of a Novel Therapeutic Approach for Managing Cardiovascular Disease
Synthetic Genomics
2023-06-07
EGAS50000000124
Study-25-07-2023
Exome Sequencing
2023-07-25
EGAS50000000125
Study createine_5
Exome Sequencing
2023-08-23
EGAS50000000127
Study 08
Exome Sequencing
2023-08-24
EGAS50000000134
Study-29-0-2023
Whole Genome Sequencing
2023-08-29
EGAS50000000135
The complete sequence of a human genome
Whole Genome Sequencing
2023-08-23
EGAS50000000136
Study title 01.09.2023
Whole Genome Sequencing
2023-09-01
EGAS50000000137
Study title 02.09.2023
Metagenomics
2023-09-02
EGAS50000000144
two_files 13-09-2023
Whole Genome Sequencing
2023-09-13
EGAS50000000145
study two_files 13-09-2023 exe2
Metagenomics
2023-09-13
EGAS50000000146
Study 13-09-2023 exe3
Whole Genome Sequencing
2023-09-13
EGAS50000000147
Study title 14-09-2023 Test 1
Metagenomics
2023-09-14
EGAS50000000151
Study 15-09-2023 Test 1
Whole Genome Sequencing
2023-09-15
EGAS50000000153
My title
Whole Genome Sequencing
2023-09-18
EGAS50000000154
Genomic map of Poland in open access - digitization of biomolecular resources of the Biobank University of Lodz laboratory
Exome Sequencing
2023-09-20
EGAS50000000155
25-09-2023 test 1
Whole Genome Sequencing
2023-09-25
EGAS50000000156
Study title 2 25-09-2023 test 1
Whole Genome Sequencing
2023-09-25
EGAS50000000158
My title
Whole Genome Sequencing
2023-09-26
EGAS50000000191
Clinical data of breast cancer patients from EuCanImage - Use case 7
Cancer Genomics
2023-10-10
EGAS50000000194
Submission 32 - study_title 1
Forensic or Paleo-genomics
2023-10-19
EGAS50000000195
Submission 32 - study_title 2
Metagenomics
2023-10-19
EGAS50000000196
Study_File_24
Whole Genome Sequencing
2023-10-20
EGAS50000000197
Synthetic - FEGA Sweden TEST vSALG4
Whole Genome Sequencing
2023-10-19
EGAS50000000198
Test study
Whole Genome Sequencing
2023-10-20
EGAS50000000199
Synthetic - FEGA Sweden Helpdesk vOQK92 v99JPF study title TEST
Whole Genome Sequencing
2023-10-20
EGAS50000000200
1Gib-subm
Whole Genome Sequencing
2023-10-23
EGAS50000000201
some studie
Whole Genome Sequencing
2023-10-24
EGAS50000000202
2023-10-24-01-study
Metagenomics
2023-10-24
EGAS50000000203
2023-10-23-02-10gib-study-title
Whole Genome Sequencing
2023-10-24
EGAS50000000206
Submission 36 - study_title 1
Epigenetics
2023-10-27
EGAS50000000207
Submission 36 - study_title 2
Epigenetics
2023-10-27
EGAS50000000208
Submission 37 - study_title 1
Whole Genome Sequencing
2023-10-27
EGAS50000000209
Submission 37 - study_title 2
Metagenomics
2023-10-27
EGAS50000000210
2023-10-29-01-file-40
Whole Genome Sequencing
2023-10-29
EGAS50000000212
2023-10-31-01
Whole Genome Sequencing
2023-10-31
EGAS50000000213
Submission 129 - study_title 2
Metagenomics
2023-11-02
EGAS50000000214
Submission 129 - study_title 1
Transcriptome Sequencing
2023-11-02
EGAS50000000216
2023-11-12-01
Whole Genome Sequencing
2023-11-12
EGAS50000000217
2023-11-08-02
Metagenomics
2023-11-07
EGAS50000000219
Study Test 05
Exome Sequencing
2023-08-23
EGAS50000000220
2023-11-19-01 studies title
Whole Genome Sequencing
2023-11-18
EGAS50000000221
2023-11-19-02
Whole Genome Sequencing
2023-11-18
EGAS50000000222
Test study for FEGA.pl
Whole Genome Sequencing
2023-11-20
EGAS50000000225
Submission 135 - study_title 2
Exome Sequencing
2023-11-21
EGAS50000000226
Submission 135 - study_title 2
Transcriptome Analysis
2023-11-21
EGAS50000000227
Open Genome Map of Poland
Whole Genome Sequencing
2023-11-23
EGAS50000000228
Synthetic - Demo submission Heilsa project meeting 2023
Whole Genome Sequencing
2023-11-24
EGAS50000000233
2023-11-30-01
Whole Genome Sequencing
2023-11-30
EGAS50000000234
Submission 150 - study_title 1
Epigenetics
2023-12-01
EGAS50000000235
Submission 150 - study_title 2
Transcriptome Analysis
2023-12-01
EGAS50000000236
Submission 151 - study_title 1
Forensic or Paleo-genomics
2023-12-01
EGAS50000000237
Submission 151 - study_title 2
Resequencing
2023-12-01
EGAS50000000242
Submission study test UGT
Whole Genome Sequencing
2023-12-08
EGAS50000000243
local test
Whole Genome Sequencing
2023-12-11
EGAS50000000249
Submission 157 - study_title 1
Pooled Clone Sequencing
2023-12-12
EGAS50000000250
Submission 157 - study_title 2
Exome Sequencing
2023-12-12
EGAS50000000251
Submission 141 - study_title 2
Synthetic Genomics
2023-11-30
EGAS50000000252
Submission 141 - study_title 1
Population Genomics
2023-11-30
EGAS50000000255
test 4
Whole Genome Sequencing
2023-12-12
EGAS50000000256
Submission 161 - study_title 1
RNASeq
2023-12-13
EGAS50000000257
Submission 161 - study_title 2
Transcriptome Sequencing
2023-12-13
EGAS50000000258
2023-12-05-01
Whole Genome Sequencing
2023-12-05
EGAS50000000259
2023-12-14-01
Whole Genome Sequencing
2023-12-13
EGAS50000000260
Submission 163 - study_title 1
Synthetic Genomics
2023-12-19
EGAS50000000261
Submission 163 - study_title 2
Metagenomics
2023-12-19
EGAS50000000264
Synthetic mini dataset
Whole Genome Sequencing
2024-01-15
EGAS50000000267
Submission 168 - study_title 1
Pooled Clone Sequencing
2024-01-22
EGAS50000000268
Submission 168 - study_title 2
Whole Genome Sequencing
2024-01-22
EGAS50000000269
test swiss study
Whole Genome Sequencing
2024-02-16
EGAS50000000270
Submission for splitting
Whole Genome Sequencing
2024-02-02
EGAS50000000271
Submission 174 - study_title 1
Metagenomics
2024-02-19
EGAS50000000272
Submission 174 - study_title 2
Pooled Clone Sequencing
2024-02-19
EGAS50000000273
2-step-test
Synthetic Genomics
2024-02-21
EGAS50000000275
2024-03-11 Tommy Study title
Whole Genome Sequencing
2024-03-11
EGAS50000000276
Indexed alignement
Whole Genome Sequencing
2024-03-18
EGAS50000000277
Single CRAM demo local
Whole Genome Sequencing
2024-03-19
EGAS50000000278
before demo study
Whole Genome Sequencing
2024-03-20
EGAS50000000279
study 2 before demo
Whole Genome Sequencing
2024-03-20
EGAS50000000280
Technical DEMO
Whole Genome Sequencing
2024-03-20
EGAS50000000281
bla bla study
Whole Genome Sequencing
2023-11-20
EGAS50000000282
Badanie populacyjne
Whole Genome Sequencing
2023-11-23
EGAS50000000283
2023-12-11-01
Whole Genome Sequencing
2023-12-11
EGAS50000000286
Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing
Whole Genome Sequencing
2023-06-15
EGAS50000000287
test
Whole Genome Sequencing
2024-04-17
EGAS50000000288
19-04-2024_1-study
Whole Genome Sequencing
2024-04-19
EGAS50000000289
19-04-2024_2
Whole Genome Sequencing
2024-04-19
EGAS50000000290
test-study-20240422
Whole Genome Sequencing
2024-04-22
EGAS50000000291
Open Genome Map of Poland
Whole Genome Sequencing
2024-04-23
EGAS50000000292
Study for upgrade test dataset 2024-04-26
RNASeq
2024-04-26
EGAS50000000293
Study_Test_2024-04-25
Whole Genome Sequencing
2024-04-25
EGAS50000000294
Study_Test_2024-04-25_2
Whole Genome Sequencing
2024-04-25
EGAS50000000296
Submission 188 - study_title 1
Population Genomics
2024-05-13
EGAS50000000297
Submission 188 - study_title 2
Population Genomics
2024-05-13
EGAS50000000298
Submission 16 - study_title 1
Whole Genome Sequencing
2023-05-19
EGAS50000000299
Submission 16 - study_title 2
Resequencing
2023-05-19
EGAS50000000310
Submission 201 - study_title 1
Exome Sequencing
2024-06-06
EGAS50000000311
Submission 201 - study_title 2
Exome Sequencing
2024-06-06
EGAS50000000318
DATA-859 dry run testing of CGA
Whole Genome Sequencing
2024-06-10
EGAS50000000325
demo
Whole Genome Sequencing
2024-06-12
EGAS50000000326
Submission 209 - study_title 1
Synthetic Genomics
2024-06-13
EGAS50000000327
Submission 209 - study_title 2
RNASeq
2024-06-13
EGAS50000000330
18-06-2024
Whole Genome Sequencing
2024-06-17
EGAS50000000331
hands-on play pretest study
Whole Genome Sequencing
2024-06-18
EGAS50000000333
Find something interesting
Resequencing
2024-06-19
EGAS50000000334
This is for CGA demo: Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read Sequencing-June 19
Whole Genome Sequencing
2024-06-19
EGAS50000000335
Test: This is for CGA demo: Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read SequencingTest
Whole Genome Sequencing
2024-06-19
EGAS50000000338
This is for CGA demo: Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read Sequencin
Whole Genome Sequencing
2024-06-20
EGAS50000000341
Submission 219 - study_title 1
Forensic or Paleo-genomics
2024-06-20
EGAS50000000342
Submission 219 - study_title 2
Pooled Clone Sequencing
2024-06-20
EGAS50000000351
Submission 240 - study_title 1
Transcriptome Sequencing
2024-07-04
EGAS50000000352
Submission 240 - study_title 2
Metagenomics
2024-07-04
JGAS000001
Identification and Characterization of Cancer Mutations in Japanese LungAdenocarcinoma without Sequencing of Normal Tissue Counterparts
Exome Sequencing
2014-07-17
JGAS000002
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
Whole Genome Sequencing
2014-09-03
JGAS000004
Genomic and Genetic Analysis of Brain Tumors and Analysis of Their Clinicopathological Significance
Tumor vs. Matched-Normal
2014-09-07
JGAS000005
Gene expression of human Th17 cells before and after activation
Transcriptome Analysis
2014-09-08
JGAS000006
DNA methylation dynamics during early human development
Whole genome bisulfite sequencing
2014-10-28
JGAS000007
Research for genetic causes and mechanisms of Hirschsprung's or Hirschsprung's related diseases
Exome Sequencing
2014-10-30
JGAS000008
Research for candidate genes of splenic epidermoid cyst
Exome Sequencing
2014-11-03
JGAS000009
Whole exome sequence analysis in multiple system atrophy
Case-Control
2014-11-19
JGAS000011
Systematic identification of long non-coding RNAs potentially involved in gastrointestinal carncer
Transcriptome Sequencing
2014-12-21
JGAS000012
Genotype data from Nagahama cohort project
Cohort
2014-12-23
JGAS000013
Whole exome sequence analysis in sporadic amyotrophic lateral sclerosis
Case Set
2015-01-06
JGAS000014
Genetic analysis in monozygotic twins discordant for bipolar disorder
Control Set
2015-01-05
JGAS000015
DNA methylation at HBV integrants and flanking host genomes
Tumor vs. Matched-Normal
2015-01-14
JGAS000016
Genetic analysis in lifestyle-related disease, arteriosclerotic disease, and aging-related diseases.
Case Set
2015-01-22
JGAS000017
Leukemic evolution of donor-derived cells harboring IDH2 and DNMT3A mutations after allogeneic stem cell transplantation
Exome Sequencing
2015-02-01
JGAS000018
An imputation reference panel of HLA variants in Japanese
Control Set
2015-03-03
JGAS000021
Genomics characterization of primary central nervous system lymphoma
Exome Sequencing
2015-03-04
JGAS000022
Integrated copy number and expression analysis identifies profiles of whole-arm chromosomal alterations and subgroups with favorable outcome in ovarian clear cell carcinomas
Tumor vs. Matched-Normal
2015-03-17
JGAS000023
Whole-exome sequencing of MDS and related myeloid neoplasms
Tumor vs. Matched-Normal
2015-04-14
JGAS000024
Identification of genetic polymorphism on aggressive periodontitis
Case Set
2015-03-26
JGAS000026
Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (WGBS)
Control Set
2015-06-01
JGAS000027
Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (ChIP-seq)
Control Set
2015-05-07
JGAS000028
Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (RNA-Seq)
Control Set
2015-04-27
JGAS000032
Effective screening strategy for deafness using a new-genetation sequencing platform: a consecutive analysis
Case Set
2015-08-23
JGAS000035
Searching for rare/low frequency variants in rheumatoid arthritis by exome sequencing
Exome Sequencing
2015-08-28
JGAS000036
Whole-exome sequencing of pediatric solid tumors
Tumor vs. Matched-Normal
2015-09-05
JGAS000037
Development of molecular targeted therapy for small cell lung cancer by comprehensive genome analysis
Case Set
2015-09-23
JGAS000038
Parent-of-origin dependent DNA methylation and gene expression in the human placenta
Whole Genome Sequencing
2015-10-06
JGAS000039
Analysis of TKI resistant mechanism for gastrointstinal stromal tumor
Exome Sequencing
2015-10-19
JGAS000040
Identification of genetic polymorphism on aggressive periodontitis
Case Set
2015-10-24
JGAS000041
Genetic analysis in an inherited cardiac arrhythmia
Case-Control
2015-10-27
JGAS000042
Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from normal individuals
Case-Control
2015-11-10
JGAS000043
Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Schizophrenia individuals
Case-Control
2015-11-10
JGAS000044
Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Depression individuals
Case-Control
2015-11-10
JGAS000045
Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Bipolar disorder individuals
Case-Control
2015-11-10
JGAS000046
Genome-wide copy number analysis of neuroblastoma
SNP array analysis
2015-12-20
JGAS000047
Transcriptome analysis of adolescents and young adults with Acute Lymphoblastic Leukemia
Transcriptome Sequencing
2016-01-06
JGAS000051
Japanese Alzheimer's disease neuroimaging initiative
Cohort
2016-02-04
JGAS000052
Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies
Tumor vs. Matched-Normal
2016-02-23
JGAS000053
Transcriptome analysis of Hepatitis B for drug discovery and clinical applications
Transcriptome Sequencing
2016-03-06
JGAS000057
Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs
Case Set
2016-05-25
JGAS000059
Genetic and epigentic analysis of non-alcoholic fatty liver disease. Methylation analysis of nonalcoholic fatty liver.
Control Set
2016-06-22
JGAS000060
Investigating genomic intratumor heterogeneity in colorectal carcinoma
Case-Control
2016-07-07
JGAS000061
Geriatric Oncology Database of genotypes and methylation, gene expression, clinical data, and survey results on psychosocial and physical conditions in Japanese elderly cancer patients to establish truly effective treatment strategy
Case Set
2016-07-11
JGAS000062
Identification of new molecular targets with profiling of malignant mesothelioma
Exome Sequencing
2016-07-08
JGAS000064
RNA expression profiling of neuromuscular diseases and viral diseases
Transcriptome Sequencing
2016-08-15
JGAS000065
Sequencing cancer mutations in various types of lung cancer using the long-read, portable sequencer
Case Set
2016-08-15
JGAS000068
RNA-sequence analysis in patients with inclusion body myositis
Case Set
2016-08-31
JGAS000070
CAGE analysis for non-small cell lung carcinoma
Transcriptome Sequencing
2016-09-20
JGAS000073
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Transcriptome Sequencing
2016-10-03
JGAS000075
Intractable Cancer Therapy Development through a New Target Identification by Molecular Profiling
Tumor vs. Matched-Normal
2016-10-14
JGAS000076
Project for Development of Innovative Research on Cancer Therapeutics; Identifiying the predictive factors for response to chemoherapy in ovarian cancer
Tumor vs. Matched-Normal
2016-10-18
JGAS000077
RNA-seq analysis of BMP-stimulated glioma initiating cells
Transcriptome Sequencing
2016-10-27
JGAS000078
Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [BS-Seq ]
Control Set
2016-11-13
JGAS000079
Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [ ChIP-Seq ]
Control Set
2016-11-13
JGAS000080
Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [RNA-Seq ]
Control Set
2016-11-13
JGAS000081
Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [RNA-Seq ]
Control Set
2016-12-05
JGAS000082
Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [BS-Seq ]
Control Set
2016-12-05
JGAS000085
Expression quantitative trait loci analysis using human immune cells in a Japanese population
Expression quantitative trait loci analysis
2017-02-05
JGAS000086
Identification of genetic mutations characteristic for recurrence and metastasis of gastric cancer.
Tumor vs. Matched-Normal
2016-12-30
JGAS000087
Identification of genetic mutations characteristic for recurrence and metastasis of lymphoma.
Tumor vs. Matched-Normal
2017-01-08
JGAS000088
Genome-wide integrative analysis of pediatric pancreatoblastoma
Exome Sequencing
2017-02-28
JGAS000089
Project for Development of Innovative Research on Cancer Therapeutics;Shuttle system between petient-derived xenograft and ex vivo culture for innovative platform of evaluating drug sensitivity.
Tumor vs. Matched-Normal
2017-01-10
JGAS000090
Whole transcriptome sequencing of pediatric T-cell acute lymphoblastic leukemia
Transcriptome Sequencing
2017-01-18
JGAS000091
Identification of genetic mutations characteristic for recurrence and metastasis of colon and rectal cancer.
Tumor vs. Matched-Normal
2016-12-21
JGAS000092
intratumor heterogeneity in colorectal adenoma and carcinoma
Tumor vs. Matched-Normal
2017-02-06
JGAS000093
POU4F3 mutation screening in Japanese hearing loss patients.
Case Set
2017-03-16
JGAS000094
The elucidation of molecular mechanisms of hematopoietic stem cells focusing on paroxysmal nocturnal hemoglobinuria (PNH)-type cells
Tumor vs. Matched-Normal
2017-02-21
JGAS000095
High-coverage whole-genome sequencing reveals structural variations in triple-negative breast cancer
Whole Genome Sequencing
2017-03-09
JGAS000096
WGS analysis of a glioma initiating cell line
Whole Genome Sequencing
2017-03-10
JGAS000098
Targeted exome sequencing identify compound heterozygous TYK2 mutations in patients with primary immunodeficiency who developed EBV-associated lymphoma
Family
2017-04-03
JGAS000099
mutation analysys of Gorlin syndrome
Exome Sequencing
2017-04-17
JGAS000101
GWAS for atrial fibrillation in the Japanese population
Case-Control
2017-04-18
JGAS000103
Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
Transcriptome sequencing (Tumor only)
2017-05-24
JGAS000104
Identification of genetic mutations characteristic for recurrence of serous ovarian cancer.
Tumor vs. Matched-Normal
2017-04-14
JGAS000105
High-coverage whole exome sequence in non-TRU-type lung adenocarcinomas
Exome Sequencing
2017-05-31
JGAS000106
Molecular analysis of diffuse cerebellar gliomas
Tumor vs. Matched-Normal
2017-06-04
JGAS000107
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Transcriptome Sequencing
2017-06-04
JGAS000108
Genomic DNA analysis for malignant mesothelioma from the patients of Japan and USA.
Tumor vs. Matched-Normal
2017-06-04
JGAS000109
Genome sequencing of biliary tract cancers
Whole Genome Sequencing
2017-05-23
JGAS000111
Searching for DNA methylation sites associated with panic disorder
Case-Control
2017-06-22
JGAS000112
Epigenome analysis of human trophoblast stem cells
Transcriptome Sequencing
2017-06-28
JGAS000113
Comprehensive genomic analysis of colorectal cancer with microsatellite instability
Exome Sequencing
2017-07-02
JGAS000114
Biobank Japan genotype and phenotype data
GWAS
2017-07-27
JGAS000115
BHD-associated kidney cancer
Tumor vs. Matched-Normal
2017-08-29
JGAS000119
Identification of RNA biomarkers in Parkinson's disease patients
Case-Control
2017-09-26
JGAS000120
419 Japanese healthy control
Control Set
2017-10-01
JGAS000121
Controlling cell differentiation with precision through understanding the structure and dynamics of gene regulatory networks
transcriptome, microarray
2017-10-02
JGAS000122
Development of humanized mice for human hematopoisis and immunity research
Exome Sequencing
2017-10-16
JGAS000123
WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis
Case Set
2017-12-03
JGAS000124
CAGE analysis for endometrial carcinoma
Transcriptome Sequencing
2017-12-04
JGAS000125
Neuron-specifc methylome analysis of Alzheimer's disease brain
Methylome analysis
2017-12-06
JGAS000126
Genome-wide analysis for non alcoholic fatty liver disease
Case-Control
2018-02-06
JGAS000127
Innate myeloid cell sbuset-specific gene expression patterns in the human colon are altered in Crohn's disease patients
Transcriptome Sequencing
2018-03-01
JGAS000128
Comprehensive gene analysis of colorectal cancer cases
Exome Sequencing
2018-03-18
JGAS000129
Identification of the genes associated with EGFR-mutant lung cancer
Case Set
2018-03-20
JGAS000130
Molecular Profiling and Sequential Somatic Mutation Shift in Hypermutator Tumors Harboring POLE Mutations
Tumor vs. Matched-Normal
2018-03-28
JGAS000131
Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors
ChIP Sequencing
2018-04-03
JGAS000132
Transcriptome analysis of Williams syndrome
Case-Control
2018-04-05
JGAS000134
Clonal structure and oncogenic potential of liver cirrhosis tissues.
Tumor vs. Matched-Normal
2018-05-10
JGAS000135
Treg cell subset-specific gene expression patterns in human head and neck cancer
Transcriptome Sequencing
2018-05-22
JGAS000136
Research for drug discovery and elucidation of pathophysiology using disease-specific iPS cells
Exome Sequencing
2018-05-29
JGAS000137
Whole genome sequencing and mutation rate analysis of Vietnamese trios with paternal dioxin exposure
Whole Genome Sequencing
2018-05-29
JGAS000138
DNA methylation array analysis of pediatric T-cell acute lymphoblastic leukemia
DNA methylation array
2018-06-05
JGAS000139
Development of the prevention and therapy of CRC using patient derived culture tissues.
Case-Control
2018-06-13
JGAS000140
Target sequencing of 11 hereditary breast cancer genes in Japanese
Case-Control
2018-06-06
JGAS000141
Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
Transcriptome sequencing (Tumor only)
2018-07-02
JGAS000142
Identification of RNA biomarkers in Parkinson's disease iPSC-derived neuronal cells
Case-Control
2018-07-04
JGAS000144
A multicenter study of susceptibility genes to type 1 diabetes
Case-Control
2018-07-17
JGAS000145
Na?ve Treg-specific genomic DNA hypomethylation for autoimmune disease susceptibility
Whole Genome Sequencing
2018-08-01
JGAS000146
DNA demethylation is associated with malignant progression of low-grade gliomas
Tumor vs. Matched-Normal
2018-08-06
JGAS000147
Transcriptome sequencing, DNA methylation analysis, and SNP array analysis of acute lymphoblastic leukemia in Down syndrome
Transcriptome Sequencing
2018-08-21
JGAS000149
The exploratory research of diagnositic biomarker and therapeutic targets of renal cell carcinoma.
Transcriptome Sequencing
2018-09-12
JGAS000150
Genetic and transcriptional landscape of plasma cells in POEMS syndrome
Transcriptome Sequencing
2018-09-15
JGAS000151
WGS analysis of Japanese liver cancer
Tumor vs. Matched-Normal
2018-06-18
JGAS000153
Gene expression analysis for nasal polyps
Transcriptome Sequencing
2018-10-17
JGAS000155
Whole genome sequencing analysis of esophageal squamous cell carcinoma
Tumor vs. Matched-Normal
2018-10-25
JGAS000156
Whole genome sequencing analysis of hepatoblastoma
Tumor vs. Matched-Normal
2018-10-26
JGAS000157
Whole genome sequencing analysis of colorectal cancers
Tumor vs. Matched-Normal
2018-10-23
JGAS000158
Prediction of response to preoperative chemoradiotherapy in rectal cancer based on whole-exome sequencing and transcriptomic analysis
Tumor vs. Matched-Normal
2018-10-29
JGAS000159
3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals
Cohort
2018-12-04
JGAS000160
Susceptibility loci for tanning ability in Japanese population identified by genome-wide association study
GWAS
2018-12-05
JGAS000162
Whole exome sequencing of familial MDS, Two patients
Exome Sequencing
2018-12-17
JGAS000164
Comprehensive assay for the molecular profiling of cancer by target enrichment from formalin-fixed paraffin-embedded specimens
Target sequencing
2019-02-04
JGAS000165
Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [ ChIP-Seq ]
Control Set
2019-02-13
JGAS000166
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients.
Case Set
2019-03-26
JGAS000169
Whole exome sequencing of uterine adenomyosis
Exome Sequencing
2019-03-25
JGAS000170
Transcriptome analysis of Familial dysautonomia patient cells treated with splice-regulating compounds
Transcriptome Sequencing
2019-04-07
JGAS000171
C-MACH reduced-representation bisulfite sequencing (RRBS)
RRBS
2019-04-04
JGAS000172
Comprehensive sequencing analyses of uterine and ovarian carcinosarcoma
Tumor vs. Matched-Normal
2019-04-09
JGAS000173
Building a Database of Genomic Structural Variants in Japanese population
Control Set
2019-04-17
JGAS000174
Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis
Tumor vs. Matched-Normal
2019-04-21
JGAS000176
Genomic Structural Variants in Japanese Malignant mesothelioma patients
Case Set
2019-04-27
JGAS000177
Integrated Exome and RNA Sequencing of Dedifferentiated Liposarcoma
Tumor vs. Matched-Normal
2019-05-09
JGAS000178
Comprehensive genomic analysis of patient derived orthotopic xenograft model in primary central nervous system lymphoma
Exome Sequencing
2019-05-17
JGAS000179
Identification of driver oncogenes in scirrhous-type gastric cancer cell lines
Exome Sequencing
2019-05-22
JGAS000180
Nanopore whole-genome sequencing of sample RK067 and variant-call data (SNVs and intermediate-sized deletions) of 174 Japanese samples.
Whole Genome Sequencing
2019-05-28
JGAS000182
Analysis of genomic alterations in dedifferentiated liposarcoma
Tumor vs. Matched-Normal
2019-06-09
JGAS000186
Shotgun metagenome sequencing of saliva samples using PromethION
Control Set
2019-06-20
JGAS000188
Integrated multi-omics analysis of pediatric hepatoblastoma
Transcriptome Sequencing
2019-06-26
JGAS000189
Target sequencing of ROS1-rearranged lung cancer patients
Target capture sequencing
2019-07-10
JGAS000190
Whole-genome sequencing on hepatocellular carcinoma with nodule-in-nodule appearance reveals stepwise cancer evolution
Whole Genome Sequencing
2019-07-12
JGAS000191
CLDN14 mutation identifed from Japanese sensorineural hearing loss patient.
Case Set
2019-07-21
JGAS000192
Mutational Spectrums and Clinical Features of Patients with LOXHD1 Variants Identified in a 8,074 Hearing Loss Patient Cohort.
Case Set
2019-07-22
JGAS000194
Viral integration analysis of hepatocellular carcinoma using virus capture sequence.
Virus Capture Sequencing
2019-07-23
JGAS000196
Targeted sequencing of cell free DNA samples from oligometastatic colorectal cancer patients
Case Set
2019-08-05
JGAS000197
Whole-genome bisulfite sequencing for high-grade glioma
Whole-genome bisulfite sequencing
2019-07-07
JGAS000198
Identification of therapeutic target molecules for prostate cancer by using next generation sequencer
Transcriptome Sequencing
2019-08-26
JGAS000199
Somatic inflammatory gene mutations accumulate in human ulcerative colitis epithelium
Exome Sequencing
2019-08-29
JGAS000200
Mid-frequency hearing loss is a characteristic clinical feature of OTOA-associated hearing loss
Case Set
2019-09-01
JGAS000201
The prevalence and clinical characteristics of TECTA-associated autosomal dominant hearing loss.
Case Set
2019-09-01
JGAS000202
Genomic Profiling Reveals Heterogeneous Populations of Ductal Carcinoma In Situ
Tumor vs. Matched-Normal
2019-09-09
JGAS000203
Target sequencing of 8 hereditary prostate cancer genes in Japanese
Case-Control
2019-09-04
JGAS000204
Comprehensive genetic analysis of pediatric germ cell tumors
Transcriptome Sequencing
2019-10-02
JGAS000205
Elucidation of disease state by multi-layered omics analysis
Population
2019-10-02
JGAS000206
Establishment of an integrated database for clinical and genomic data in cancer
Targeted capture sequence
2019-10-07
JGAS000207
Epigenomic analysis of human androgenetic trophoblast stem cells derived from complete hydatidiform mole
Transcriptome Sequencing
2019-10-22
JGAS000211
Elucidation of genomic pathology of a patient with concurrent acute myeloid leukemia and mediastinal germ cell tumor
Exome Sequencing
2019-12-17
JGAS000214
comprehensive genetic analysis and database construction for head and neck cancer
Exome Sequencing
2020-01-05
JGAS000215
Comprehensive molecular and clinicopathological profiling of lung adenocarcinoma in Japanese never or light smokers
Exome Sequencing
2020-01-07
JGAS000216
Whole exome sequencing of surgically resected lung adenocarcinomas and gastric adenocarcinomas.
Exome Sequencing
2020-01-20
JGAS000217
Sequence analysis of colorectal serrated lesions
Case Set
2020-01-26
JGAS000218
Expression profiling of Gorlin iPSCs in the osteoblast induction culture
Case-Control
2020-02-13
JGAS000220
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2020-03-23
JGAS000221
The genetic analysis of circulating tumor DNA in blood of the digestive cancer patients to investigate the prognostic factors of metastasis and reccurence.
Tumor vs. Matched-Normal
2020-03-25
JGAS000222
Ten colorectal cancer patients with locally advanced primary tumors who underwent primary tumor resection following neoadjuvant chemotherapy (NAC).
Tumor vs. Matched-Normal
2020-03-25
JGAS000223
Influence of pre-analytical processing on blood protein profiles (AMED-Metabolites)
Quantitative proteomics
2020-03-26
JGAS000224
Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
Tumor vs. Matched-Normal
2020-03-26
JGAS000225
Transcriptome analysis of Fabry disease iPSC-derived cardiomyocytes treated with splice-regulating compound; RECTAS
Transcriptome Sequencing
2020-04-02
JGAS000226
Mortality and risk of progression to adult T-cell leukemia/lymphoma in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis
Tumor vs. Matched-Normal
2020-04-02
JGAS000227
Whole exome sequencing of patients with esophageal squamous cell carcinoma receiving chemoradiotherapy
Tumor vs. Matched-Normal
2020-04-06
JGAS000228
Defined Lifestyle and Germline Factors Predispose Asian Populations to Gastric Cancer
Exome Sequencing
2020-04-09
JGAS000229
Defined Lifestyle and Germline Factors Predispose Asian Populations to Gastric Cancer
Exome Sequencing
2020-04-12
JGAS000230
Identification and characterization of molecular markers in aging and neuronal disorders
Transcriptome Sequencing
2020-04-29
JGAS000231
Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA
Tumor vs. Matched-Normal
2020-05-26
JGAS000232
The analysis of gene mutations in Hematology malignancy
Exome Sequencing
2020-06-10
JGAS000233
Genome and gene analysis of gastrointestinal cancer and elucidation of its clinicopathological significance
Exome Sequencing
2020-05-17
JGAS000234
Genomic and transcriptomic analysis on hepatocarcinogenesis after HCV eradication
Case-Control
2020-06-15
JGAS000236
Paediatric Hepatic International Tumour Trial (JPLT2: PHITT)
Exome Sequencing
2020-06-18
JGAS000237
An Organoid Biobank of Rare Human Neuroendocrine Neoplasms Enables Genotype-Phenotype Mapping
Whole Genome Sequencing
2020-06-25
JGAS000238
Demographic History and Local Adaptation in Asian Population
Population
2020-07-09
JGAS000239
TMM whole genome analysis of 4566 Japanese individuals
Cohort
2020-07-15
JGAS000240
Inherited chromosomally-integrated human herpesvirus 6A/B (HHV-6A/B) genome sequences in the Japanese population
Whole Genome Sequencing
2020-07-19
JGAS000241
Genomic profiling identified ERCC2 helicase domain mutations respond to platinum-based neoadjuvant therapy in urothelial bladder cancer
Tumor vs. Matched-Normal
2020-07-20
JGAS000242
Immunogenomic analysis of tumor infiltrating B cells in gastric cancer
Repertoire sequencing (Tumor vs. Matched-Normal)
2020-07-20
JGAS000243
Frequent post-treatment monitoring of colorectal cancer using individualized ctDNA validated by multi-regional molecular profiling
Tumor vs. Matched-Normal
2020-07-27
JGAS000244
Whole exome sequencing of solid tumors which received PD-1 blockade therapy
Exome Sequencing
2020-07-28
JGAS000245
Identifying aberrant splicing isoforms and potential neoantigens in non-small cell lung cancer
Tumor vs. Matched-Normal
2020-07-27
JGAS000246
Multi-omics analysis of pediatric high-risk neuroblastoma
Transcriptome Sequencing
2020-07-30
JGAS000248
CAGE-seq analysis of osteoblast derived from cleidocranial dysplasia human induced pluripotent stem cells
Transcriptome Sequencing
2020-08-27
JGAS000249
Pilot study of adoptive cell therapy using cultured tumor infiltrating lymphocytes for Japanese melanoma patients refractory to immune-checkpoint inhibitors
Exome Sequencing
2020-09-07
JGAS000253
Development of hunanized mice for human hematopoisis and immunity research
Transcriptome Sequencing
2020-09-18
JGAS000256
Gene expression data of 2D duodenum organoids with or without continuous flow
RNA Sequencing
2020-10-11
JGAS000257
Cell-free DNA sequencing using newly developed single-strand DNA library preparation
Whole Genome Sequencing
2020-10-13
JGAS000258
Whole genome sequence analysis in patients with primary central nervous system lymphomas
Exome Sequencing
2020-10-25
JGAS000259
Japanese Reference Genome JG1
Whole Genome Sequencing
2020-11-03
JGAS000260
Elucidation of disease state by multi-layered omics analysis
Population
2020-11-23
JGAS000262
Hi-C analysis of patient-derived pancreas neoplasm organoids
Hi-C
2020-12-07
JGAS000263
Whole exome sequencing and RNA sequencing of patient-derived pancreas neoplasm organoids
Exome Sequencing
2020-12-07
JGAS000264
ATAC-seq and ChIP-seq analysis of patient-derived normal pancreas and pancreas neoplasm organoids
ATAC sequencing
2020-12-07
JGAS000265
Long-read methylation analysis of breast cancer using the enzymatic base conversion and the nanopore sequencing
Tumor vs. Matched-Normal
2020-12-14
JGAS000267
Identification of biomarkers for prediction of efficacy of microtubule inhibitors and antifolates in non-small cell lung cancer
Case Set
2021-01-17
JGAS000269
Comprehensive analyses of genetic aberrations in gastroenterological tumors
Exome Sequencing
2021-01-12
JGAS000270
Comprehensive molecular and clinicopathological profiling of desmoid tumors
Exome Sequencing
2021-01-21
JGAS000272
Clinical and neuroimaging study on preclinical Alzheimer's disease.
Longitudinal
2021-01-17
JGAS000273
Whole exome sequencing of 69 trios with bipolar disorder
Exome Sequencing
2021-03-02
JGAS000274
PanCancer genome analysis in 5143 Japanese cancer patients
Tumor vs. Matched-Normal
2021-03-03
JGAS000276
Comprehensive genomic analysis for AYA with acute lymphoblastic leukemia
Transcriptome Sequencing
2021-03-11
JGAS000277
Brain Mapping by Integrated Neurotechnologies for Disease Studies: Human Brain Aging Imaging Study
Clinical Trial
2021-03-09
JGAS000278
Phase II clinical trial of adult Philadelphia chromosome-negative precursor B-cell acute lymphocytic leukemia with combination chemotherapy
Transcriptome Sequencing
2021-03-11
JGAS000279
Whole exome sequencing of colorectal cancer
Exome Sequencing
2021-03-15
JGAS000280
Proteogenomic discovery of a novel class of cancer antigens by HLA ligandome analysis of colon cancer tissues
Transcriptome Sequencing
2021-03-28
JGAS000281
Single B cell analysis in pemphigus patients
Transcriptome Sequencing
2021-03-31
JGAS000282
NGS-based targeted exome sequencing of osteosarcoma
Tumor vs. Matched-Normal
2021-04-04
JGAS000285
Whole exome sequencing, RNA sequencing and single-cell RNA sequencing of 4 melanoma patients
Exome Sequencing
2021-04-19
JGAS000286
Building a Database of Genomic Structural Variants in Japanese population
Control Set
2021-03-15
JGAS000288
Total NF1 sequence in the patients with neurofaibromatosis type1
Case Set
2021-05-06
JGAS000289
The single plasma-cell transcriptional landscape in POEMS syndrome
Transcriptome Sequencing
2021-04-04
JGAS000290
Efficient prediction of a spatial transcriptomics profile better characterizes breast cancer tissue sections without costly experimentation
Case Set
2021-05-06
JGAS000292
Comprehensive analysis of the abnormality of the genes in juvenile myelomonocytic leukemia
Methylation analysis
2021-05-16
JGAS000293
Combined landscape of single-nucleotide variants and copy-number alterations in clonal hematopoiesis
Population
2021-05-18
JGAS000294
Whole Transcriptome Sequencing of NXF1 or CRM1 depleted Cell
Transcriptome Sequencing
2021-05-18
JGAS000295
Sensitive gene analysis of hereditary cardiovascular disease
Case Set
2021-05-17
JGAS000296
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2021-06-01
JGAS000297
Comprehensive molecular profiling of pulmonary pleomorphic carcinoma
Exome Sequencing
2021-06-02
JGAS000300
Phylogenetic analysis of combined lobular and ductal carcinoma of the breast
Tumor vs. Matched-Normal
2021-06-06
JGAS000301
Genetic drivers define transcriptomic characteristics and clonal hierarchy within intratumoral heterogeneity in adult T-cell leukemia-lymphoma
Tumor vs. Matched-Normal
2021-06-09
JGAS000303
Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors .
Single Cell RNA Sequencing
2021-06-15
JGAS000304
Mutational anysis of breast cancer stem cells
Case Set
2021-06-17
JGAS000305
Single cell RNA seq of breast cancer stem cells
Population
2021-06-17
JGAS000307
Genetics of diffuse large B-cell lymphoma in Japan
targeted DNA sequencing
2021-06-21
JGAS000308
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Gene panel sequencing
2021-06-23
JGAS000309
Single cell transcriptome analysis of breast invasive carcinoma
Transcriptome Sequencing
2021-06-27
JGAS000310
Genome sequence comparison of human iPS cell lines
Whole Genome Sequencing
2021-07-06
JGAS000311
Elucidation of molecular mechanism of NAFLD-HCC
Case-Control
2021-07-06
JGAS000312
CCR8-targeted specific depletion of clonally expanded Treg cells in tumor tissues evokes potent tumor immunity with long-lasting memory
Transcriptome Sequencing
2021-07-06
JGAS000313
Whole-exome sequencing of Helicobacter pylori-uninfected normal gastric gland
Control Set
2021-07-08
JGAS000314
KIR imputation panel
Control Set
2021-07-14
JGAS000316
Elucidation of disease state by multi-layered omics analysis
Population
2021-07-29
JGAS000317
Mechanisms on relapse after allogeneic hematopoietic cell transplantation in CMML
Transcriptome Sequencing
2021-07-29
JGAS000318
Identification of RNA biomarkers in Parkinson's disease iPSC-derived neuronal cells
Case-Control
2021-07-30
JGAS000320
Whole Genome Sequencing Analysis of Adult T-cell Leukemia/Lymphoma
Whole Genome Sequencing
2021-08-04
JGAS000321
Comprehensive analysis of interaction between human gene expression and environmental metagenomes.
Cohort
2021-08-10
JGAS000323
Prevalence and Clinical Characteristics of hearing loss caused by MYH14 mutation
Case Set
2021-08-01
JGAS000325
Targeted sequencing of vascular malformations tissues and paired blood samples
Tumor vs. Matched-Normal
2021-08-18
JGAS000327
Target sequencing of 27 cancer-predisposing genes in Japanese pancreatic cancer patients
Case-Control
2021-08-26
JGAS000330
Development of blood-based biomarkers for precision medicine in castration-resistant prostate cancer
Cohort
2021-09-06
JGAS000335
Exploration of predictive biomarkers for postoperative recurrence of stage II/III colorectal cancer using genomic sequencing
Exome Sequencing
2021-09-15
JGAS000341
Response to Hepatitis B vaccine
Case-Control
2021-09-26
JGAS000346
Target sequencing of 27 cancer-predisposing genes in Japanese colorectal cancer patients
Case-Control
2021-09-05
JGAS000347
Impact of germline pathogenic variants in 27 cancer-predisposing genes on the risk of lymphoma
Case-Control
2021-09-05
JGAS000348
Whole-genome analysis of a healthy man with common trichromatic vision
Whole Genome Sequencing
2021-09-27
JGAS000349
Analysis of chromosomal background of cancerous mutations using a long-read sequencer
Tumor vs. Matched-Normal
2021-09-28
JGAS000350
The characterization of gene expression pattern of anticancer agent-resistant cancer stem cells using RNA sequencing analysis.
Transcriptome Sequencing
2021-09-30
JGAS000359
Elucidation of molecular mechanisms of tumorigenesis and development of diagnoses and treatments based on comprehensive genomic analyses in pancreatic tumors, duodenal tumors and biliary tumors
Tumor vs. Matched-Normal
2021-10-06
JGAS000360
Different malignant tumor samples including lung cancer, colon cancer and breast cancer.
Tumor vs. Matched-Normal
2021-10-07
JGAS000361
Whole genome analysis of liver cancer by long-read sequencing
Whole Genome Sequencing
2021-10-10
JGAS000367
Whole exome sequencing and RNA-seq of esophageal squamous cell carcinoma
Tumor vs. Matched-Normal
2021-10-17
JGAS000368
Comprehensive molecular profiling for breast cancer patients and high-risk individuals.
Target sequencing
2021-10-21
JGAS000370
Discovering novel mechanisms of taxane resistance in human breast cancer by whole-exome sequencing
Exome Sequencing
2021-10-25
JGAS000377
Comprehensive molecular profiling of subsequent solid cancers after allogenic hematopoietic cell transplantation
Exome Sequencing
2021-11-03
JGAS000378
The RNA, ChIP and whole exome sequencing analysis of human colorectal cancer organoids and normal colon organoids treated with (+)-JQ1
Transcriptome Sequencing
2021-11-03
JGAS000379
Filtered variants including SLC12A2 in patients with hearing loss
Parent-Offspring Trios
2021-11-04
JGAS000381
Biobank Japan WGS data of myocardial infarction and dementia
Whole Genome Sequencing
2021-11-08
JGAS000382
Transcriptome analysis of iPSC-derived hepatocytes from Wilson's Disease patients and healthy controls
Case-Control
2021-10-21
JGAS000383
Analysis of the relationship between disease phenotype and genotype in patients with Alzheimer's disease
Case Set
2021-11-18
JGAS000385
Multi-omics characterization of KMT2A-rearranged infant acute lymphoblastic leukemia
Transcriptome Sequencing
2021-11-18
JGAS000387
Semibulk RNA-seq analysis as a convenient method for measuring gene expression statuses in a local cellular environment
Tumor vs. Matched-Normal
2021-11-23
JGAS000389
Genome sequencing of biliary tract cancers
Whole Genome Sequencing
2021-11-24
JGAS000412
Biobank Japan genotype data
Biobank
2021-11-23
JGAS000413
Genetic analysis of non-small cell lung cancer patients and PDX tumor harboring driver gene alteration
Exome Sequencing
2021-11-30
JGAS000414
Target sequencing of 27 cancer-predisposing genes and 13 renal cell carcinoma-related genes in Japanese renal cell carcinoma patients
Case-Control
2021-12-06
JGAS000415
Whole gut virome analysis of 476 Japanese revealed a link between phage and autoimmune disease
Population
2021-12-08
JGAS000416
Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
Transcriptome Sequencing
2021-12-12
JGAS000417
Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
Transcriptome Sequencing
2021-12-12
JGAS000418
Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
Transcriptome Sequencing
2021-12-12
JGAS000454
The impact of CCR8+ regulatory T cells on cytotoxic T cell function in human lung cancer
Transcriptome Sequencing
2021-12-14
JGAS000480
Single cell sequences in patients with malignant tumors
single cell RNA sequence
2021-12-14
JGAS000482
Myasthenia gravis-specific aberrant neuromuscular gene expression by medullary thymic epithelial cells in thymoma
Transcriptome Sequencing
2021-12-16
JGAS000483
Target sequencing of refractory adult Ph-negative B-ALL 1 patient
Case Set
2021-12-20
JGAS000485
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2021-12-21
JGAS000486
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2021-12-22
JGAS000487
Common and rare germline variants in Japanese prostate cancer patients
Cohort
2021-12-22
JGAS000488
exploration of biomarkers discriminating squamous cell carcinoma from other lung cancers
Transcriptome Sequencing
2022-01-10
JGAS000489
exploration of biomarkers in colorectal cancer
Transcriptome Sequencing
2022-01-10
JGAS000490
Mutation screening in a large series of Japanese hearing loss patients using massively parallel DNA sequencing analysis.
Case Set
2022-01-10
JGAS000504
Genetic architecture of microRNA expression and its link to complex diseases in the Japanese population
Population
2022-02-02
JGAS000505
Building a Database of Genomic Structural Variants in Japanese population
Control Set
2022-02-02
JGAS000507
Whole exome sequence and transcliptomic analysis of tumor tissues with hepatocellular carcinoma and metastatic liver cancer
Exome Sequencing
2022-02-09
JGAS000508
Microarray genotyping of idiopathic hypersomnia patients (11 orexin mutation-positive patients, 85 orexin mutation-negative patients)
Case Set
2022-02-18
JGAS000510
A study on personalized medicine in genitourinary cancers using genetic biomarkers
Tumor vs. Matched-Normal
2022-03-02
JGAS000514
HNF1B induced three-dimentional genome analysis of patient-derived pancreas neoplasm organoids
Transcriptome Sequencing
2022-03-21
JGAS000515
Bisulfite sequencing of cell-free DNA in NMOSD patients
Case-Control
2022-03-23
JGAS000516
Comprehansive analysis of somatic mutations and genetic variations with whole genome sequencing
RNA-seq
2022-03-27
JGAS000520
An efficient procedure for the recovery of DNA from formalin-fixed paraffin-embedded tissue sections
Whole Genome Sequencing
2022-04-13
JGAS000522
Next-generation sequencing-based comprehensive genetic analysis of undiagnosed disease
Exome Sequencing
2022-04-18
JGAS000523
Elucidation of molecular mechanism of NAFLD-HCC
Tumor vs. Matched-Normal
2022-04-18
JGAS000528
Single cell RNA sequencing of human cord Blood CD34 Cells
Mutiomics
2022-05-15
JGAS000529
Molecular profiling for a patient with lipoblastoma-like tumor of the vulva
Whole Genome Sequencing
2022-05-15
JGAS000530
Metagenome shotgun sequencing of the Inflammatory Bowel Disease
Case-Control
2022-05-18
JGAS000531
Reconstruction of the microbial genomes from the Japanese gut metagenome
Population
2022-05-19
JGAS000532
Identification of potential blood biomarkers for early diagnosis of Alzheimer���s disease through immune landscape analysis
Case-Control
2022-05-19
JGAS000533
Genomic features of renal cell carcinoma developed in end-stage renal disease and dialysis
Whole Genome Sequencing
2022-05-09
JGAS000534
Comprehensive molecular and clinicopathological profiling of salivary duct carcinoma
Tumor vs. Matched-Normal
2022-05-19
JGAS000535
Immuno-genomic Profiling of Biopsy Specimens Predicts Neoadjuvant Chemotherapy Response in Esophageal Squamous Cell Carcinoma
Tumor vs. Matched-Normal
2022-05-22
JGAS000537
Analysis of ATL progression by CD30 signaling and its biomarkers (2)
Exome Sequencing
2022-05-22
JGAS000538
Immunohistochemical and molecular pathological search in gastrointestinal tumors
Tumor vs. Matched-Normal
2022-05-15
JGAS000540
New classification of occlusive cerebrovascular diseases by combining diagnostic imaging and genetic analysis of RNF213
Case-Control
2022-06-12
JGAS000541
Biobank Japan genotype data
Biobank
2022-04-19
JGAS000543
Single-cell RNA-sequencing for peripheral blood mononuclear cells from COVID-19 patients and healthy controls of Japanese
Case-Control
2022-07-14
JGAS000544
Whole genome, whole exome and transcriptome sequencing of 10 ccRCC with Von Hippel-Lindau disease
Whole Genome Sequencing
2022-07-14
JGAS000545
Analytical study of protein function and RNA expression involved in predicting treatment efficacy and adverse event development in lung cancer radiotherapy.
Cohort
2022-07-14
JGAS000546
Multimodal single-cell analyses of peripheral blood mononuclear cells in COVID-19 patients
Case Set
2022-07-18
JGAS000548
Targeted Capture DNA Sequencing
Targeted Capture DNA Sequencing
2022-07-21
JGAS000549
Loss of presentation of estimated neoantigens from mutated genes in ctDNA was essential for fostering primary to recurrent tumors in postoperative colorectal cancer cases
Case Set
2022-07-21
JGAS000550
single-cell RNA-sequencing of human/mouse colonic crypts
Transcriptome Sequencing
2022-07-25
JGAS000551
Single cell RNA sequencing of human umbilical cord blood lymphoid progenitors
single cell RNA sequencing
2022-07-28
JGAS000553
Durable clinical impacts and mechanisms of action and resistance in histone K27 methylation-targeting epigenetic therapy
Tumor vs. Matched-Normal
2022-08-17
JGAS000557
Research for biological features by gene expression analysis and biomarkers at diagnosis/therapeutics in lung cancer
Multi-omics data
2022-08-29
JGAS000558
Target sequencing of a case of concurrent Langerhans Cell Histiocytosis and Acute Myeloid Leukemia
Case Set
2022-09-19
JGAS000559
Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with distinctive genome-wide DNA hypomethylation
Whole Genome Bisulfite Sequencing
2022-09-19
JGAS000561
NMR metabolic biomarkers in Biobank Japan generated by Nightingale Health Japan
Biobank
2022-09-20
JGAS000562
A study of resistance to novel coronavirus infection in health care workers
Cohort
2022-09-25
JGAS000563
Observational study on the immune responses acquired by COVID-19 convalescent individuals
Transcriptome Sequencing
2022-09-29
JGAS000564
Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors .
Whole Genome Sequencing
2022-10-03
JGAS000568
NGS sequencing for genes from the patients of OU Genome Project
Case Set
2022-10-06
JGAS000569
The role of gut microbiota in metabolic diseases
Transcriptome Sequencing
2022-10-07
JGAS000570
Whole-genome sequencing analysis for understanding of the stepwise progression of lung adenocarcinoma
Whole Genome Sequencing
2022-10-06
JGAS000572
Metabolome analysis of persons with type 2 diabetes with or without diabetic complications
Case-Control
2022-11-01
JGAS000573
Induction of fetal meiotic oocytes from embryonic stem cells in cynomolgus monkeys
Whole Genome Sequencing
2022-11-03
JGAS000574
16S metagenomics on NASH patients complicated with diabetes
Case-Control
2022-11-03
JGAS000575
Genomic features of Helicobacter pylori-na��ve diffuse-type gastric cancer.
Tumor vs. Matched-Normal
2022-11-03
JGAS000578
Autoimmune-wide landscape of circulating CD4+ T cells unveils disease-specific heritability and phenotypic changes
Transcriptome Sequencing
2022-11-21
JGAS000579
Target resequencing of LQTS-related 100 genes in Japanese patients
Case Set
2022-11-23
JGAS000580
Building a Database of Genomic Structural Variants in Japanese population
Control Set
2022-11-24
JGAS000582
Whole exome sequencing and RNA sequencing of cervical cancer
Exome Sequencing
2022-11-30
JGAS000585
Establishment of xenogfafts and cultured cell lines from clinical samples
Target Capture Sequencing
2022-12-15
JGAS000586
Whole exome sequencing and RNA sequencing of cervical cancer
Exome Sequencing
2022-12-18
JGAS000587
Whole genome sequencing of AML with FUS-ERG
Whole Genome Sequencing
2022-12-23
JGAS000588
Comprehensive biomarker analysis from phase II study of nivolumab in patients with thymic carcinoma
Clinical Trial
2022-12-25
JGAS000591
Highly prevalent NF-kappa B signaling pathway-activating somatic mutations in intracranial aneurysms
Case-Control
2023-01-22
JGAS000592
Germline pathogenic variant and gastric cancer risk
Case-Control
2023-01-15
JGAS000593
Single-cell RNA-sequencing for peripheral blood mononuclear cells from COVID-19 patients and healthy controls of Japanese
Case-Control
2023-01-30
JGAS000596
Building a Database of Genomic Structural Variants in Japanese population
Control Set
2023-02-23
JGAS000597
Comprehensive analyses of genetic aberrations in cholangiolocarcinoma
Exome Sequencing
2023-02-26
JGAS000598
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2023-02-27
JGAS000599
Comprehensive analyses of clinicopathological features and genomic mutations of combined hepatocellular-cholangiocarcinoma
Exome Sequencing
2023-02-28
JGAS000600
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Population
2023-02-28
JGAS000602
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2023-03-08
JGAS000604
Whole genome sequencing, DNA methylation, and gene expression data from gastrointestinal stromal tumor 30 patients
Whole Genome Sequencing
2023-03-12
JGAS000605
A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion
methylome analysis
2023-03-21
JGAS000609
Research for biological features by gene expression analysis and biomarkers at diagnosis/therapeutics in lung cancer
Multi-omics data
2023-05-01
JGAS000610
Research for biological features by gene expression analysis and biomarkers at diagnosis/therapeutics in lung cancer
Multi-omics data
2023-05-01
JGAS000611
Mitochondrial DNA Mutations at Low-level Heteroplasmy in Chronic Kidney Disease
Amplicon Sequencing
2023-05-08
JGAS000617
Transcriptome sequencing of fibroblast-dependent alveolar organoids derived from patient-specific iPS cells with SFTPC^Y104H variant and their gene-corrected (monoallelic wild type SFTPC) ones.
Transcriptome Sequencing
2023-06-12
JGAS000618
Development of cell lines and mouse models of bone and soft tissue sarcoma to establish novel treatment
Exome Sequencing
2023-06-20
JGAS000619
Exploratory novel biomarker and resistance mechanism of milademetan, an MDM2 inhibitor, in MDM2 amplified intimal sarcoma from an open-label phase 1b/2 trial ���NCCH1806/MK004���
Case Set
2023-06-25
JGAS000621
Gene expression signatures associated with chronic endometritis revealed by RNA sequencing
Transcriptome Sequencing
2023-06-29
JGAS000622
Variant allele frequency changes in TP53 predict pembrolizumab response in patients with metastatic urothelial carcinoma
Target sequencing
2023-06-29
JGAS000623
Research on the identification of cancer stem cells for peidatric and adult malignancies.
Case Set
2023-06-29
JGAS000625
Investigation of molecular diagnosis by molecular biological analysis using next-generation sequencer for actionable endocrine diseases (including neoplastic diseases)
Parent-Offspring Trios
2023-07-12
JGAS000626
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2023-07-17
JGAS000627
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2023-07-17
JGAS000628
RNA sequencing of skin tissue and peripheral blood mononuclear cells from patients with atopic dermatitis and healthy controls.
Transcriptome Sequencing
2023-07-17
JGAS000638
Study for establishment for effective screening and diagnosis of Lynch syndrome
Cohort hereditary tumor
2023-09-26
JGAS000640
single-cell RNA sequencing and RNA sequencing of normal uterine cervix
Transcriptome Sequencing
2023-10-11
JGAS000643
CRISPR-screening identifies mechanisms of resistance to KRASG12C and SHP2 inhibitor combinations in non-small cell lung cancer
Transcriptome Sequencing
2023-10-30
JGAS000645
Whole exome sequencing of external auditory canal squamous cell carcinoma (EACSCC)
Exome Sequencing
2023-10-31
JGAS000646
Genetic alterations that deregulate RB and PDGFRA signaling pathways drive tumor progression in IDH2-mutant astrocytoma
Exome Sequencing
2023-11-05
JGAS000647
Asian Genome Project(BioBank Japan genotype data)
Whole Genome Sequencing
2023-10-30
JGAS000648
Integrative understanding of human immune system by functional genomics and development of intervention strategies for the prevention of autoimmune diseases
Transcriptome Sequencing
2023-11-06
JGAS000651
RNA sequencing of genetically modified human iPSCs modeling patients with autism spectrum disorders (ASD)
Transcriptome Sequencing
2023-11-13
JGAS000657
Establishing stable brain tumor stem cell lines and translational research for new treatments
Whole Genome Sequencing
2023-12-14
JGAS000659
CRISPR screening in human trophoblast stem cells reveals both shared and distinct aspects of human and mouse placental development
Whole Genome Sequencing
2023-12-24
JGAS000661
Discovery of genetic factors associated with thiopurine-induced severe adverse events
GWAS
2023-12-26
JGAS000668
Case-control study with RNA-seq transcriptome between ASD patients and non ASD controls.
Transcriptome Sequencing
2024-01-29
JGAS000671
Comprehensive molecular and clinicopathological profiling of glioma
Transcriptome Sequencing
2024-02-12
phs000001
National Eye Institute (NEI) Age-Related Eye Disease Study (AREDS)
Case-Control
2012-01-05
phs000007
Framingham Cohort
Longitudinal
2021-07-08
phs000016
International Multi-Center ADHD Genetics Project
Parent-Offspring Trios
2009-11-24
phs000017
Whole Genome Association Study of Bipolar Disorder
Case-Control
2008-07-14
phs000018
Search for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants), GAIN
Case-Control
2014-09-18
phs000019
Collaborative Association Study of Psoriasis
Case-Control
2008-01-07
phs000020
Major Depression: Stage 1 Genomewide Association in Population-Based Samples
Case-Control
2008-09-22
phs000021
Genome-Wide Association Study of Schizophrenia
Case-Control
2010-10-22
phs000048
Mayo-Perlegen LEAPS (Linked Efforts to Accelerate Parkinson's Solutions) Collaboration
Case-Control
2008-01-07
phs000086
Diabetes Control and Complications Trial (DCCT) and Epidemiology of Diabetes Interventions and Complications Study (EDIC)
Clinical Trial
2014-08-07
phs000088
Search for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants and parents), NIDDK
Case-Control
2008-01-16
phs000089
NINDS-Genome-Wide Genotyping in Parkinson's Disease: First Stage Analysis and Public Release of Data
Case-Control
2010-03-30
phs000090
The Atherosclerosis Risk in Communities (ARIC) Study
Case-Cohort
2008-01-15
phs000091
GENEVA Genes and Environment Initiatives in Type 2 Diabetes (Nurses' Health Study/Health Professionals Follow-up Study)
Nested Case-Control
2009-06-30
phs000092
Study of Addiction: Genetics and Environment (SAGE)
Case-Control
2008-01-15
phs000093
A Genome Wide Scan of Lung Cancer and Smoking
Case-Control
2009-10-08
phs000094
International Consortium to Identify Genes and Interactions Controlling Oral Clefts
Case Set
2008-01-15
phs000095
Dental Caries: Whole Genome Association and Gene x Environment Studies
Case-Control
2021-06-15
phs000096
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study - Maternal Glycemia and Birthweight GEI Study
Prospective
2011-08-30
phs000100
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study
Case-Control
2011-04-11
phs000101
Mega-GWAS ALS I
Case-Control
2018-03-02
phs000102
Ischemic Stroke Genetics Study (ISGS)
Case-Control
2008-01-07
phs000103
Genome-Wide Association Studies of Prematurity and Its Complications
Nested Case-Control
2008-01-15
phs000122
Whole Genome Association Study of Systemic Lupus Erythematosus
Case-Control
2008-01-16
phs000124
Neuroblastoma Genome-Wide Association Study (NBL-GWAS)
Case-Control
2010-12-10
phs000125
CIDR: Collaborative Study on the Genetics of Alcoholism Case Control Study
Case-Control
2008-02-26
phs000126
CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD)
Case-Control
2016-02-09
phs000127
A Genome-Wide Association Study of Sporadic ALS in an Irish Population (SIALS) and Sequencing and Analysis of an Irish Human Genome
Case-Control
2010-09-03
phs000128
GAW16 Framingham and Simulated Data
Longitudinal
2010-07-21
phs000130
NIDDK IBD Genetics Consortium Crohn's Disease Genome-Wide Association Study
Case-Control
2008-03-17
phs000138
GWAS for Genetic Determinants of Bone Fragility in European-American Premenopausal Women
Quantitative Cross-Sectional
2010-04-29
phs000139
International Multiple Sclerosis Genomics Consortium (IMSGC) Genome Wide Association Study of Multiple Sclerosis
Parent-Offspring Trios
2008-05-14
phs000140
A Whole Genome Association Search for Type 2 Diabetes Genes in African Americans
Case-Control
2008-06-27
phs000142
A Whole Genome Association Scan for Myopia and Glaucoma Endophenotypes using Twin Studies
Twin
2008-07-18
phs000143
Starr County Health Studies' Genetics of Diabetes Study
Case-Control
2008-07-15
phs000144
National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma
Tumor vs. Matched-Normal
2008-08-18
phs000145
POPRES: Population Reference Sample
Population
2013-03-06
phs000147
Cancer Genetic Markers of Susceptibility (CGEMS) Breast Cancer Genome-wide Association Study (GWAS) - Primary Scan: Nurses' Health Study - Additional Cases: Nurses' Health Study 2
Case-Control
2015-02-19
phs000153
FHS-Net Social Networks
Longitudinal
2015-07-06
phs000159
Genomics of Acute Myeloid Leukemia
Tumor vs. Matched-Normal
2022-12-30
phs000160
National Institute on Aging (NIA) Late-Onset Alzheimer's Disease Genetics Initiative: The Multiplex Family Study
Family
2008-10-17
phs000166
National Heart, Lung, and Blood Institute SNP Health Association Asthma Resource Project (SHARP)
Longitudinal
2009-07-21
phs000167
Molecular Genetics of Schizophrenia - nonGAIN Sample (MGS_nonGAIN)
Case-Control
2008-11-04
phs000168
National Institute on Aging - Late Onset Alzheimer's Disease Family Study: Genome-Wide Association Study for Susceptibility Loci
Family
2012-03-29
phs000169
Whole Genome Association Study of Visceral Adiposity in the Health Aging and Body Composition (Health ABC) Study
Longitudinal
2008-12-16
phs000170
A Genome-Wide Association Study on Cataract and HDL in the Personalized Medicine Research Project Cohort
Case-Control
2012-08-02
phs000171
A Case-Controlled Study for Genotype-Phenotype Associations in Multiple Sclerosis (MS)
Case-Control
2009-02-03
phs000178
National Institutes of Health The Cancer Genome Atlas (TCGA)
Tumor vs. Matched-Normal
2019-12-03
phs000179
Genetic Epidemiology of COPD (COPDGene) Funded by the National Heart, Lung, and Blood Institute
Case-Control
2017-11-15
phs000180
Type 1 Diabetes Genetics Consortium (T1DGC): Genome-Wide Association Study in Type 1 Diabetes, 2008
Case Set
2014-08-01
phs000181
Genomewide Association Study of Alcohol Use and Alcohol Use Disorder in Australian Twin-Families (OZ-ALC GWAS)
Twin
2009-02-27
phs000182
Age related Macular Degeneration (AMD)-- Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: A Joint Genome Wide Association Study
Case-Control
2010-03-22
phs000185
Genetic Studies in the Hutterites
Cross-Sectional
2021-10-25
phs000187
High Density SNP Association Analysis of Melanoma: Case-Control and Outcomes Investigation
Case-Control
2009-04-02
phs000188
Vanderbilt Genome-Electronic Records (VGER) Project: QRS Duration
Case Set
2009-04-28
phs000196
Genome-Wide Association Study of Parkinson Disease: Genes and Environment
Case-Control
2015-03-20
phs000199
Children's Hospital of Philadelphia (CHOP) Control Copy Number Variation (CNV) Study
Control Set
2009-06-12
phs000200
Women's Health Initiative Clinical Trial and Observational Study
Partial Factorial Randomized
2018-06-01
phs000201
Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes
Tumor vs. Matched-Normal
2014-04-08
phs000202
OMRF SLEGEN GWAS Data from European-American Women with Lupus
Case-Control
2009-06-16
phs000203
A Genome-Wide Association Study of Peripheral Arterial Disease
Case-Control
2009-06-17
phs000204
Genetic Analysis of Limb Malformation Disorders: Freeman Sheldon Syndrome Exome Sequencing Study (LMD-FSS)
Exome Sequencing
2009-06-24
phs000205
International Standards for Cytogenomic Arrays
Clinical Genetic Testing
2015-01-21
phs000206
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Case-Control
2015-07-10
phs000207
Cancer Genetic Markers of Susceptibility (CGEMS) Prostate Cancer Genome-Wide Association Study (GWAS) - Primary Scan (Stage 1) - PLCO Screening Trial
Nested Case-Control
2009-07-22
phs000209
Multi-Ethnic Study of Atherosclerosis (MESA) Cohort
Longitudinal
2014-05-01
phs000210
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Nested Case-Control
2009-08-18
phs000211
National Institute of General Medical Sciences (NIGMS) Human Genetic Cell Repository Human Variation Panels including 100 African-Americans (HD100AA), 100 Caucasians (HD100CAU), 100 Han People of Los Angeles (HD100CHI) and 100 Mexican American Community of Los Angeles (HD100MEX)
Population-Based Control Set
2009-08-24
phs000215
Genome-Wide Association Analysis of Biomarkers in the InCHIANTI and BLSA
Population
2013-05-20
phs000216
International Consortium on the Genetics of Systemic Lupus Erythematosus (SLEGEN)
Case-Control
2009-09-15
phs000217
Genome-Wide Association Study of Leprosy and Dapsone Hypersensitivity Syndrome (DHS) in Chinese population
Case-Control
2018-11-08
phs000218
National Cancer Institute (NCI) TARGET: Therapeutically Applicable Research to Generate Effective Treatments
Cohort
2023-02-16
phs000219
Multi-Site Collaborative Study for Genotype-Phenotype Associations in Alzheimer's disease and Longitudinal follow-up of Genotype-Phenotype Associations in Alzheimer's disease and Neuroimaging component of Genotype-Phenotype Associations in Alzheimer's disease
Case-Control
2009-10-01
phs000220
Population Architecture using Genomics and Epidemiology (PAGE): Multiethnic Cohort (MEC)
Cohort
2013-05-17
phs000221
NHLBI Family Heart Study (FamHS-Visit1 and FamHS-Visit2)
Family
2009-10-26
phs000222
PREDICT-HD Huntington Disease Study
Observational
2017-10-27
phs000223
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Atherosclerosis Risk in Communities (ARIC)
Longitudinal
2009-11-03
phs000224
VitGene Generalized Vitiligo Genetics Study-Phase 2
Case-Control
2016-02-11
phs000225
A Population Genomics Study Using a Disease-Targeted Cell model: Integration of
eQTL
2009-11-04
phs000226
STAMPEED: Cardiovascular Health Study (CHS) GWAS to identify genetic variants associated with aging and CVD risk factors and events
Longitudinal
2011-05-27
phs000228
NIH Human Microbiome Project - Core Microbiome Sampling Protocol A (HMP-A)
Population-Based Control Set
2017-03-21
phs000233
Genome Wide Association Study of Asthma
Case-Control
2009-12-02
phs000234
Development and Use of Network Infrastructure for High-Throughput GWA Studies
Case-Control
2015-11-12
phs000235
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
Cohort
2022-06-17
phs000236
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Coronary Artery Risk Development in Young Adults (CARDIA)
Longitudinal
2009-12-18
phs000237
Northwestern NUgene Project: Type 2 Diabetes
Case-Control
2010-01-20
phs000238
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Case-Control
2010-02-01
phs000239
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
Case-Control
2010-07-21
phs000240
National Eye Institute (NEI) Ocular Hypertension Treatment Study (OHTS)
Clinical Trial
2010-02-23
phs000244
Genetic Analysis of Limb Malformation Disorders: Miller Syndrome Sequencing Study (LMD-MS)
Exome Sequencing
2010-03-09
phs000245
Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples
Tumor vs. Matched-Normal
2010-03-12
phs000247
The Neonatal Microbiome and Necrotizing Enterocolitis
Case-Control
2017-05-19
phs000248
Genetic Determinants of Viral Clearance in HCV-Infected Populations
Case-Control
2010-03-26
phs000249
Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain
Control Set
2013-12-06
phs000250
CALGB 80303:Genome-Wide Association Study of Advanced Pancreatic Cancer Patients - A Randomized Phase III trial of Gemcitabine Plus Bevacizumab versus Gemcitabine Plus Placebo in Patients with Advanced Pancreatic Cancer
Clinical Trial
2010-04-01
phs000251
Human Microbiome Project Demonstration Study of Cutaneous Microbiome in Psoriasis
Case-Control
2013-09-19
phs000252
Diet, Genetic Factors, and the Gut Microbiome in Crohn's Disease
Cross-Sectional
2011-01-06
phs000253
Human Liver Cohort (HLC)
Population
2010-04-19
phs000254
ARRA - NHLBI Lung Cohorts Sequencing Project: Genetic modifiers of
Cohort
2012-10-04
phs000255
Effect of Crohn's Disease Risk Alleles on Enteric Microbiota
Case-Control
2010-04-26
phs000256
The Vaginal Microbiome: Disease, Genetics and the Environment
Twin
2019-05-14
phs000257
Metagenomic Analysis of the Structure and Function of the Human Gut Microbiota in Crohn's Disease
Twin
2012-10-25
phs000258
The Thrifty Microbiome: The Role of the Gut Microbiota in Obesity in the Amish
Longitudinal
2011-01-06
phs000259
Urethral Microbiome of Adolescent Males
Longitudinal
2011-01-18
phs000260
Foregut Microbiome in Development of Esophageal Adenocarcinoma
Case-Control
2015-09-10
phs000261
The Microbial Ecology of Bacterial Vaginosis: A Fine Scale Resolution Metagenomic Analysis
Cohort
2020-10-08
phs000262
Ulcerative Colitis Human Microbiome Project (UCHMP)
Longitudinal
2013-01-08
phs000263
Metagenomic study of the human skin microbiome associated with acne
Case-Control
2010-05-03
phs000264
The Human Virome in Children and its Relationship to Febrile Illness
Prospective
2011-03-04
phs000265
The Human Gut Microbiome and Recurrent Abdominal Pain in Children
Case-Control
2011-05-04
phs000266
Skin Microbiome in Disease States: Atopic Dermatitis and Immunodeficiency
Longitudinal
2013-08-22
phs000267
Autism Genome Project (AGP) Consortium - Whole Genome Association Study of over 1,500 Parent-Offspring Trios - Stage I and II
Parent-Offspring Trios
2016-03-02
phs000268
Genotyping NIGMS CEPH Samples from the United States, Venezuela, and France
Family
2010-05-07
phs000269
Genotyping NIGMS Chromosomal Aberration and Inherited Disorder Samples
Cohort
2010-05-07
phs000272
National Institute of Arthritis and Musculoskeletal and Skin Diseases and Istanbul Faculty of Medicine Genome-wide Association Study of Behçet's Disease (Turkish)
Case-Control
2010-05-19
phs000273
High-Throughput LINE-1 Retrotransposon Discovery in Humans
Marker Discovery
2010-05-20
phs000274
Genome-Wide Association Study of Celiac Disease
Case-Control
2010-05-21
phs000275
Brigham and Women's Hospital Multiple Sclerosis Genetic Collection
Case-Control
2010-05-27
phs000276
STAMPEED: Northern Finland Birth Cohort 1966 (NFBC1966)
Longitudinal
2012-12-14
phs000277
A Genome-Wide Association Study of Heroin Dependence
Case-Control
2019-09-24
phs000279
NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI)
Longitudinal
2012-10-11
phs000280
Atherosclerosis Risk in Communities (ARIC) Cohort
Cohort
2021-07-21
phs000284
NHLBI Cleveland Family Study (CFS) Candidate Gene Association Resource (CARe)
Longitudinal
2017-02-14
phs000285
Coronary Artery Risk Development in Young Adults (CARDIA) Study - Cohort
Longitudinal
2013-04-19
phs000286
Jackson Heart Study (JHS) Cohort
Cohort
2016-08-12
phs000287
Cardiovascular Health Study (CHS) Cohort: an NHLBI-funded observational study of risk factors for cardiovascular disease in adults 65 years or older
Longitudinal
2017-12-05
phs000288
Ciliopathies Exome Sequencing Initiative
Case-Control
2014-12-17
phs000289
National Human Genome Research Institute (NHGRI) GENEVA Genome-Wide Association Study of Venous Thrombosis (GWAS of VTE)
Case-Control
2011-05-26
phs000290
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Pulmonary Arterial Hypertension)
Case-Control
2010-06-30
phs000291
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Lung Health Study of Chronic Obstructive Pulmonary Disease)
Longitudinal
2012-05-03
phs000292
Gene Environment Association Studies (GENEVA): Genetics of Early Onset Stroke (GEOS) Study
Case-Control
2010-07-09
phs000293
The Familial Intracranial Aneurysm Linkage Study (FIA)
Family Linkage
2010-07-20
phs000294
STAMPEED: Myocardial Infarction Genetics Consortium (MIGen)
Case-Control
2010-07-20
phs000295
Next Generation Mendelian Genetics: Kabuki Syndrome
Exome Sequencing
2017-12-11
phs000297
eMERGE Network Study of the Genetic Determinants of Resistant Hypertension
Case-Control
2010-07-26
phs000298
Autism Sequencing Consortium (ASC)
Case-Control
2017-12-05
phs000299
Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech
Case Set
2012-10-01
phs000302
Genetic Study on Nephropathy in Type-2 Diabetes
Case-Control
2010-08-16
phs000303
Genetic Epidemiology of Refractive Error in the KORA (Kooperative Gesundheitsforschung in der Region Augsburg) Study
Cohort
2010-08-31
phs000304
Genes and Blood Clotting Study (GABC)
Sibling Cohort
2018-05-02
phs000305
A Genome-Wide Association Study in Participants Experiencing Breast Cancer Events in High-Risk Postmenopausal Women Receiving Selective Estrogen Receptor Modulators on NSABP Trials P-1 and P-2. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Nested Case-Control
2010-09-10
phs000306
A Multiethnic Genome-wide Scan of Prostate Cancer
Nested Case-Control
2014-04-08
phs000308
The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study
Case-Control
2010-09-21
phs000309
Coronary Artery Risk Development in Young Adults (CARDIA) Study - Gene Environment Association Studies Initiative (GENEVA)
Longitudinal
2011-10-19
phs000310
Discovery of Non-ETS Gene Fusions in Human Prostate Cancer using Next Generation RNA Sequencing
Cohort
2010-10-20
phs000311
FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data
Cohort
2010-10-20
phs000313
SardiNIA Medical Sequencing Discovery Project
Family
2014-03-06
phs000314
Genetic Associations in Idiopathic Talipes Equinovarus (Clubfoot) - GAIT
Multiplex Families
2010-11-03
phs000327
NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Siblings with Ischemic Stroke Study, SWISS)
Affected Sib Pairs
2010-11-17
phs000328
Genome-Wide Analysis of Diffuse Large B-Cell Lymphoma (De Novo and Derived from the High Grade Transformation of Follicular Lymphoma)
Case-Control
2021-03-31
phs000330
The Genomic Complexity of Primary Human Prostate Cancer
Cohort
2010-12-06
phs000331
A Genome-Wide Association Study in Patients Experiencing Drug-Induced Long-QT Syndrome and/or Torsades de Pointes; A Collaboration Between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Case-Control
2023-04-25
phs000332
Genome-Wide Association Study of Preterm Birth
Case-Control
2016-01-28
phs000333
Family Investigation of Nephropathy and Diabetes (FIND) Study
Case-Control
2010-12-09
phs000335
Genome-Wide associations of Lung Health Study (LHS)
Cohort
2014-07-24
phs000336
A Genome-Wide Association Study of Lung Cancer Risk
Case-Control
2010-12-27
phs000337
Genetic Basis of Developmental Disabilities
Case Set
2010-12-27
phs000338
National Institute on Aging (NIA) SardiNIA Study
Family
2011-01-27
phs000339
Targeted MitoExome Sequencing of Mitochondrial OXPHOS Diseases (Massachusetts General Hospital)
Case Set
2013-02-05
phs000340
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Whole Genome Sequencing
2014-04-09
phs000341
The Genetic Basis of Hypodiploid ALL
Case Set
2012-10-01
phs000343
The Genomics and Randomized Trials Network (GARNET) Vitamin Intervention Stroke Prevention (VISP) Trial
Clinical Trial
2020-10-08
phs000344
Genome-Wide Association Study of Amyotrophic Lateral Sclerosis in Finland
Case-Control
2011-03-02
phs000345
NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study
Case-Control
2011-03-02
phs000346
Genome-wide association study for Bladder Cancer Risk
Case-Control
2014-08-18
phs000347
NHLBI GO-ESP: Family Studies (Thoracic aortic aneurysms leading to acute aortic dissections)
Cohort
2011-03-08
phs000348
Towards a Genomic Understanding of Myeloma
Tumor
2014-02-20
phs000349
SNPs and Extent of Atherosclerosis (SEA) Study
Cross-Sectional
2011-03-14
phs000350
Fred Hutchinson Cancer Research Center - Whole-Exome Sequencing of Hereditary Prostate Cancer Families
Family
2011-03-16
phs000351
National Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma
Cohort
2011-03-22
phs000352
The genomic complexity of sporadic and inherited retinoblastoma with a matched orthotopic xenograft
Case Set
2011-03-22
phs000353
Genome-Wide Association Studies of Prematurity and Its Complications (African American)
Case-Control
2011-03-28
phs000354
NHLBI GO-ESP Family Studies: Pulmonary Arterial Hypertension
Longitudinal
2011-03-28
phs000355
Genome Wide Association for Asthma and Lung Function
Case-Control
2011-04-04
phs000356
Population Architecture using Genomics and Epidemiology (PAGE)
Cross-Sectional
2014-08-15
phs000357
Genome-Wide Association Study in Systemic Sclerosis
Case-Control
2014-02-05
phs000358
The PUWMa (
Parent-Offspring Trios
2011-04-19
phs000359
Exome sequencing and disease analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis
Case Set
2011-04-28
phs000360
eMERGE Network Genome-Wide Association Study of Red Cell Indices, White Blood Count (WBC) Differential, Diabetic Retinopathy, Height, Serum Lipid Levels, Specifically Total Cholesterol, HDL (High Density Lipoprotein), LDL (Low Density Lipoprotein), and Triglycerides, and Autoimmune Hypothyroidism.
Case-Control
2015-11-12
phs000361
Genome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian)
Case-Control
2011-05-02
phs000362
NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation)
Cohort
2011-05-13
phs000364
High density copy number analysis and whole exome sequencing of unselected chronic lymphocytic leukemia cases and of paired chronic lymphocytic leukemia and Richter Syndrome cases
Tumor vs. Matched-Normal
2011-09-12
phs000365
Exome Sequencing for Diseases of the Immune System: X-linked Immunodeficiency with Magnesium Defect, EBV Infection, and Neoplasia (XMEN)
Case-Control
2011-06-01
phs000366
NHLBI: Genetic modifiers of sickle cell anemia severity and fetal hemoglobin expression in the Cooperative Study of Sickle Cell Disease (CSSCD)
Longitudinal
2011-06-02
phs000367
NIDDK⁄CIDR Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease
Family
2011-06-20
phs000368
Polycystic Ovary Syndrome (PCOS) Genetics
Case-Control
2011-06-20
phs000369
Sequence Analysis of Mutations and Translocations Across Breast Cancer Subtypes
Case Set
2011-06-21
phs000370
The Mutational Landscape of Head and Neck Squamous Cell Carcinoma
Case Set
2014-04-10
phs000371
Genetic Modifiers of Huntington's Disease
Cohort
2016-08-30
phs000372
Alzheimer's Disease Genetics Consortium (ADGC) Genome Wide Association Study -NIA Alzheimer's Disease Centers Cohort
Case-Control
2011-06-30
phs000373
Osteoporotic Fractures in Men (MrOS)
Cohort
2011-06-30
phs000374
Whole Genomic Sequencing of Nine Primary Colorectal Adenocarcinoma Tumor/Germline Pairs
Case Set
2011-07-01
phs000375
Genome-Wide Association of Native and Post Aspirin Platelet Function Phenotypes
Family
2011-07-01
phs000376
Whole Exome Sequencing in Familial Parkinson Disease
Family
2011-07-06
phs000378
Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria
Community
2011-07-06
phs000379
Genetic Epidemiology Network of Arteriopathy (GENOA)
Sibling Cohort
2011-07-07
phs000380
eMERGE Genome-Wide Association Studies of Obesity (Metabochip)
Case Set
2011-07-07
phs000381
eMERGE Geisinger eGenomic Medicine (GeM) - MyCode Project Controls
Control Set
2011-07-07
phs000382
CIDR Whole Exome Sequencing in Joubert Syndrome
Cohort
2014-08-12
phs000383
Genome-Wide Association Study of Breast Cancer in the African Diaspora - the ROOT study
Case-Control
2011-07-15
phs000384
Genentech whole genome and transcriptome sequencing of four hepatocellular carcinoma patients
Case Set
2011-07-25
phs000385
Epigenetic Profiling of Human Colorectal Cancer
Case Set
2011-07-28
phs000387
eMERGE Geisinger eGenomic Medicine (GeM) Abdominal Aortic Aneurysm Project (AAAP)
Case Set
2011-08-03
phs000388
Charles R. Bronfman Institute for Personalized Medicine (IPM) BioBank Genome Wide Association Study of Cardiovascular, Renal and Metabolic Phenotypes
Case-Control
2011-08-03
phs000389
GEnetics of Nephropathy - an International Effort (GENIE) GWAS of Diabetic Nephropathy in the UK GoKinD and All-Ireland Cohorts
Case-Control
2011-08-03
phs000390
Genomic Wide Scans for Female Osteoporosis Genes
Cohort
2011-08-04
phs000391
Determining Genetic Role in Treatment Response to Anti-Platelet Interventions (The PAPI Study)
Interventional
2011-08-04
phs000392
Exome sequencing of autosomal recessive progressive external ophthalmoplegia (arPEO)
Exome Sequencing
2011-08-05
phs000393
deCODE Genetics study on genes contributing to nicotine dependence in humans
Case Set
2011-08-09
phs000394
Autopsy-Confirmed Parkinson Disease GWAS Consortium (APDGC)
Case-Control
2011-08-10
phs000395
California Pacific Medical Center Research Breast Health Cohort
Nested Case-Control
2011-08-22
phs000396
Division of Cancer Epidemiology and Genetics (DCEG) Imputation Reference Dataset
Reference Set
2011-08-10
phs000397
National Institute on Aging (NIA) Long Life Family Study (LLFS)
Family
2020-06-11
phs000398
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (ARIC)
Case-Cohort
2011-08-11
phs000400
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (CHS)
Case-Cohort
2011-08-12
phs000401
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (FHS)
Case-Cohort
2011-08-12
phs000402
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (JHS)
Case-Cohort
2011-08-12
phs000404
The Genetic Architecture of Smoking and Smoking Cessation
Case-Control
2011-08-29
phs000405
Next Generation Mendelian Genetics: Malignant Hyperthermia
Case Set
2011-08-30
phs000406
Spatiotemporal Transcriptome of the Human Brain
Control Set
2011-08-31
phs000407
International Multi-Center ADHD Gene Project (IMAGE) II Case Sample
Case Set
2011-09-01
phs000408
eMERGE Genome-Wide Association Studies of Obesity
Case Set
2011-09-01
phs000409
The Genomic Analysis of Medulloblastoma
Case Set
2011-09-13
phs000410
Whole Exome Sequencing for Colorectal Cancer
Case-Control
2011-09-13
phs000413
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Case Set
2012-10-04
phs000414
Whole genome sequencing of core-binding factor leukemia
Case Set
2011-09-16
phs000415
Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families
Extended Pedigrees
2011-09-21
phs000416
Genetics of Cerebral Hemorrhage with Anticoagulation (GOCHA)
Case-Control
2017-08-21
phs000417
BrainCloud: Data from human postmortem brain procurement for the neuropathology section
Control Set
2012-01-27
phs000418
Temporal Dissection of Tumorigenesis in Primary Cancers
Tumor vs. Matched-Normal
2014-04-08
phs000419
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Family
2011-10-04
phs000421
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
Case-Control
2011-10-07
phs000422
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Case Set
2011-10-07
phs000423
Genome wide association study for early onset coronary disease and related phenotypes (ADVANCE)
Case-Control
2011-10-19
phs000424
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Reference Set
2022-04-26
phs000425
Alcohol Dependence GWAS in European- and African Americans
Case-Control
2011-10-24
phs000426
SLCO1B1 Variants and Methotrexate Clearance
Cohort
2011-10-26
phs000428
Health and Retirement Study (HRS)
Longitudinal
2013-10-18
phs000430
Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C)
Randomized Controlled Clinical Trial
2011-11-07
phs000431
GWAS for IgA Nephropathy
Case-Control
2022-05-10
phs000433
The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans
Case-Control
2011-11-07
phs000434
Next Generation Mendelian Genetics: Atypical Werner Syndrome
Case Set
2011-11-09
phs000435
Whole Exome Sequencing of Chronic Lymphocytic Leukemia
Case Set
2015-10-19
phs000436
University of Miami Study on Genetics of Autism and Related Disorders (AutismDisorders)
Multiplex Families
2011-11-17
phs000437
Next Generation Mendelian Genetics: Auriculocondylar syndrome (ACS)
Parent-Offspring Trios
2011-11-17
phs000438
A Genome-Wide Association Analysis in Angiotensin-Converting Enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine
Case-Control
2011-11-25
phs000439
A Genome-Wide Association Comparative Analysis of Response of AF Patients to Rate Control Therapy; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Case-Control
2011-11-25
phs000440
Center for Craniofacial and Dental Genetics: Study of Dental Caries and Cleft Lip/Palate in Guatemala
Nuclear Families
2011-11-25
phs000442
Drug Resistant Hypertension in African Americans' Exome
Longitudinal
2011-12-07
phs000443
Transcriptome sequencing across a prostate cancer cohort identifies PCAT-1, an unannotated lincRNA implicated in disease progression
Cohort
2011-12-21
phs000444
Italian Primary Biliary Cirrhosis Study
Case-Control
2011-12-21
phs000445
Genome Variation among HIV-Resistant People with Hemophilia
Case-Control
2012-01-06
phs000447
Prostate Cancer Genome Sequencing Project
Case Set
2012-01-12
phs000448
Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort
Case-Control
2012-01-13
phs000449
Genetic Variation and Signatures of Natural Selection in Diverse Africans
Control Set
2012-07-20
phs000450
Whole Exome Sequencing of Primary Mediastinal B-cell Lymphoma
Case Set
2021-01-25
phs000451
NHLBI and NIA The New England Centenarian Study (NECS)
Case Set
2012-01-31
phs000452
Melanoma Genome Sequencing Project
Case Set
2016-12-19
phs000454
Genome-Wide Association Study of HIV-1 Host Genetics Among Injection Drug Users
Case-Control
2019-12-10
phs000455
Molecular Genetic Studies of Developmental Brain Disorders
Cohort
2012-02-14
phs000456
Risk Assessment of Cerebrovascular Events (RACE) Study
Case-Control
2012-02-16
phs000458
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in NEIGHBOR Samples
Case-Control
2012-02-16
phs000459
Whole exome sequencing in multiplex cleft families from a consortium
Case Set
2012-02-17
phs000460
Genetics of 24 hour urine composition
Longitudinal Cohort
2012-02-17
phs000461
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples
Case-Control
2012-02-23
phs000462
T2D-GENES Project 2: San Antonio Mexican American Family Studies
Family
2012-02-29
phs000472
Estrogen Receptor Positive Breast Cancer: Aromatase Inhibitor Response Study
Tumor vs. Matched-Normal
2016-10-04
phs000473
Sweden-Schizophrenia Population-Based Case-Control Exome Sequencing
Case-Control
2015-07-21
phs000474
Biology and Molecular Analysis of Human Hematopoiesis Genetics
Probands
2015-10-22
phs000475
The molecular basis of inherited reproductive disorders
Probands
2012-03-12
phs000476
Molecular defects in pseudohypoparathyroidism or related disorders
Probands
2012-03-12
phs000477
Genetic defects in familial renal disorders
Probands
2012-03-12
phs000478
Strabismus, CCDD and other anomalies
Probands
2012-03-12
phs000479
National Heart Lung and Blood Institute Exome sequencing in SCID
Parent-Offspring Trios
2012-03-15
phs000480
Identification of Cancer Predisposition Genes in Breast Cancer Families
Family
2012-03-15
phs000481
Cholesterol and Pharmacogenetics (CAP) Study
Clinical Trial
2016-07-12
phs000482
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
Parent-Offspring Trios
2012-03-22
phs000483
Massachusetts General Hospital/Eisai National Institute of Mental Health (NIMH) Genetics Initiative Alzheimer's Disease GWAS - Affymetrix GeneChip Human Mapping 500K Array Set
Family
2012-03-22
phs000484
Molecular genetic analysis of inherited kidney dysfunction
Probands
2012-03-26
phs000485
Gene mutation and rescue in congenital diaphragmatic hernia
Probands
2012-03-26
phs000486
Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression
Cohort
2012-03-28
phs000487
Functionally Active Copy Number Variants Associated with Prostate Cancer Risk
Case-Control
2014-04-07
phs000488
Genomic Sequencing of Lung Adenocarcinoma
Case Set
2016-10-07
phs000490
A Study of the Genetic Causes of Complex Pediatric Disorders
Case Set
2012-04-10
phs000491
Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC)
Case Set
2012-04-13
phs000492
Genetics of Human Developmental Brain Disorders
Family
2023-01-11
phs000493
Genetic Association Studies in the Solomon Islanders
Case-Control
2012-04-18
phs000494
Better Outcomes for Children: GWAS from Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase II data - (dbGaP Deposit 1)
Cohort
2012-04-18
phs000495
The Gene Partnership (TGP) - eMERGE Data
Longitudinal
2012-04-20
phs000496
Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease
Case-Control
2012-04-20
phs000497
Genetic analysis of Hirschsprung disease
Probands
2016-08-01
phs000500
Non-invasive whole genome sequencing of a human fetus
Parent-Offspring Trios
2012-05-21
phs000501
Compilation of Aggregate Genomic Data for General Research Use
Aggregate Genomic Data
2012-05-23
phs000502
Genome-Wide Analysis of Splenic Marginal Zone Lymphoma
Case-Control
2012-05-29
phs000504
Medulloblastoma exome sequence analysis
Case Set
2013-10-24
phs000505
Gene Fusion Discovery through RNA Sequencing of Human Glioblastoma Stem Cell Lines
RNA Sequencing
2013-07-19
phs000507
NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS
Case-Control
2018-10-26
phs000508
Genomic Sequencing of Pediatric Rhaboid Cancers
Case Set
2014-04-07
phs000509
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Case Set
2012-06-26
phs000510
Study of Osteoporotic Fractures (SOF)
Cohort
2012-06-29
phs000511
Treatment of genetic screening of hypertriglyceridemia type I, III, and V - HTG Amsterdam
Probands
2012-07-06
phs000513
Rearrangements of the MAST Kinase and Notch Gene Families in Breast Cancer
Cohort
2012-07-10
phs000514
Identification of Genes Involved in Familial Coronary Artery Disease
Probands
2012-07-10
phs000516
Genome Sequencing of Pancreatic Ductal Adenocarcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Case Set
2015-02-13
phs000517
GWAS in African Americans, Latinos and Japanese
Case-Control
2015-05-01
phs000518
NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis of unknown etiology that is not related to cystic fibrosis or classic primary ciliary dyskinesia or immune deficiency or any other known causes
Cohort
2012-07-24
phs000519
Study of Melanoma Risk in Australia and the United Kingdom
Case Set
2012-07-24
phs000521
Episodic Ataxia Syndrome: Longitudinal Study
Longitudinal
2019-07-18
phs000522
Hyperdiploid Acute Lymphoblastic Leukemia RNA-Seq
Case Set
2012-08-01
phs000524
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Chronic Renal Insufficiency Cohort Study (CRIC)
Cohort
2012-08-02
phs000525
Expressed Pseudogenes in the Transcriptional Landscape of Human Cancers
Cohort
2012-08-07
phs000535
Whole Genome and Exon Capture Sequencing of Bladder Cancers
Cohort
2012-08-13
phs000536
Somatic L1 Retrotransposition in Colorectal Tumors
Case-Control
2015-07-29
phs000537
Next Generation Mendelian Genetics: Familial Hemophagocytic Lymphohistiocytosis
Cohort
2012-08-24
phs000538
Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
Family
2012-08-28
phs000539
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
Case Set
2012-08-29
phs000540
Next Generation Mendelian Genetics: Ehlers-Danlos Syndrome Type VIII
Case-Control
2012-08-29
phs000541
Next Generation Mendelian Genetics: Muscle Hypertrophy
Case Set
2012-08-29
phs000542
Next Generation Mendelian Genetics: Neonatal Diabetes
Case Set
2012-08-29
phs000543
Exome Sequencing of Pleuropulmonary Blastoma
Case Set
2012-08-29
phs000545
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Case-Control
2012-09-04
phs000546
NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Ischemic Stroke Genetic Study, ISGS)
Case-Control
2012-09-12
phs000547
A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial
Prospective
2012-09-12
phs000548
Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin
Cohort
2012-09-28
phs000549
Clonal Evolution of Pre-Leukemic Hematopoietic Stem Cells Precedes Human Acute Myeloid Leukemia
Case Set
2012-09-28
phs000550
Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing
Case Set
2012-09-28
phs000551
Gene Expression Signatures in CATHGEN
Case-Control
2012-10-01
phs000552
Genomic Characterization of Meningiomas
Case Set
2014-04-07
phs000553
Familial Exome Sequencing in Rare Pediatric Phenotypes
Parent-Offspring Trios
2012-10-03
phs000554
Mutational Landscape of Lethal Castrate Resistant Prostate Cancer
Tumor vs. Matched-Normal
2012-10-03
phs000556
NHLBI GO-ESP: Family Studies (JHMI-Molecular Genetics of Atypical Cystic Fibrosis (CF) Study)
Case-Control
2012-10-09
phs000558
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Case Set
2012-10-12
phs000559
Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project
Case-Control
2012-10-16
phs000560
Ecological Stressors, PTSD, and Drug Use in Detroit: The Detroit Neighborhood Health Study (DNHS)
Cohort
2021-04-29
phs000561
Metabolism and Genetics of Hypobetalipoproteinemia
Probands
2012-10-26
phs000562
The Genetic Landscape of Mutations in Burkitt Lymphoma
Tumor vs. Matched-Normal
2012-10-26
phs000563
The Genomics of Pilocytic Astrocytoma Formation in Neurofibromatosis Type 1
Case Set
2022-12-13
phs000564
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Case Set
2014-11-17
phs000565
Copy Number Variation in Congenital Kidney Malformations
Case Set
2012-11-06
phs000567
Identification of Recurrent NAB2-STAT6 Gene Fusions in Solitary Fibrous Tumor by Integrative Sequencing
Case Set
2012-11-30
phs000568
Genomic Sequencing of Solitary Fibrous Tumors
Case Set
2012-12-04
phs000571
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC)
Cohort
2015-07-30
phs000572
Alzheimer's Disease Sequencing Project (ADSP)
Case-Control
2016-06-09
phs000573
Genetic Heterogeneity of Diffuse Large B Cell Lymphoma
Case-Control
2012-12-19
phs000574
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Case Set
2012-12-28
phs000575
Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol
Case Set
2020-02-12
phs000576
Angelman, Rett, Prader-Willi Syndromes Consortium (ARP) Angelman Syndrome Natural History Protocol
Case Set
2019-07-22
phs000577
Longitudinal Study of Urea Cycle Disorders
Longitudinal
2012-12-31
phs000578
Non Dystrophic Myotonias: Genotype-Phenotype Correlation and Longitudinal
Longitudinal
2013-01-03
phs000579
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Case Set
2013-01-04
phs000580
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS)
Longitudinal Cohort
2013-01-08
phs000581
NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy)
Case Set
2013-01-08
phs000582
NHLBI GO-ESP: Family Studies (Familial Interstitial Pneumonia)
Family
2013-01-08
phs000583
Asian Indian Diabetic Heart Study (AIDHS) /Sikh Diabetes Study (SDS)
Case-Control
2013-01-10
phs000584
The Longevity Genes Project
Case-Control
2013-01-10
phs000585
International Consortium for Blood Pressure (ICBP)
Meta-Analysis
2016-08-03
phs000586
Genome Wide Association Studies in Alopecia Areata
Case Set
2013-01-24
phs000587
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Case Set
2013-01-29
phs000588
VCRC - Giant Cell Arteritis Longitudinal Study
Longitudinal
2013-01-30
phs000589
Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Takayasu's Arteritis
Longitudinal
2013-01-30
phs000590
Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Polyarteritis Nodosa
Longitudinal
2013-01-31
phs000592
Screening Protocol and Longitudinal Study of Bone Marrow Failure Syndromes and Cytopenias
Longitudinal
2013-01-31
phs000594
A Phase 2 Study of Tipifarnib in Large Granular Lymphocyte (LGL) Leukemia
Interventional
2013-02-01
phs000595
Mucociliary Clearance Consortium (MCC) Rare Genetic Disorders of the Airways: Cross-section Comparison of Clinical Features, and Development of Novel Screening and Genetic Test
Cross-Sectional
2013-02-01
phs000596
Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age
Longitudinal
2019-07-18
phs000597
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Case-Control
2013-02-01
phs000598
Exome Sequencing of Esophageal Adenocarcinoma
Case Set
2013-10-22
phs000600
Genomic Sequencing of Cervical Cancers
Case-Control
2013-02-15
phs000601
Filtering and Annotation of Variants That Are Rare (FAVR)
Family
2013-02-15
phs000602
Identification of Targetable FGFR Gene Fusions in Diverse Cancers
Case Set
2014-04-08
phs000603
Rare Genetic Steroid Disease Consortium (GSD) Apparent Mineralocorticoid Excess (AME) Syndrome Natural History Clinical Protocol
Case Set
2013-02-28
phs000604
Mapping Genes for Mammographic Density
Population
2013-03-11
phs000605
Multicenter International Lymphangioleiomyomatosis Efficacy of Sirolimus Trial (The MILES Trial)
Clinical Trial
2013-03-12
phs000606
The Incidence of Thromboembolic Events in Patients with Antibodies to Heparin-PF4 after Cardiac Bypass
Longitudinal
2013-03-12
phs000607
Neurodevelopmental Genomics: Trajectories of Complex Phenotypes
Cohort
2018-03-08
phs000608
Whole Genome Profiling to Detect Schizophrenia Methylation Markers
Case-Control
2013-03-26
phs000609
RNA-Seq studies of Gene Expression in Cells and Networks in FI and ACC in Autism
Case-Control
2013-03-29
phs000611
Whole Genome Comparisons of Breast Cancers and their Xenotransplants
Case Set
2013-04-04
phs000612
The mutational characterization of adenoid cystic carcinoma
Case-Control
2013-04-17
phs000614
Genomic Analysis of Pediatric Low Grade Gliomas
Case Set
2013-04-18
phs000615
The National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN)
Case-Control
2013-04-23
phs000616
CIP: Obesity-Diabetes Familial Risk, Viva La Familia Study
Cohort
2015-04-15
phs000617
PGRN-Leducq: Identification of the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
Case-Control
2013-04-30
phs000618
Genome-Wide Association Study of Hypertriglyceridemia in Mexicans
Case-Control
2013-05-08
phs000619
DNA Methylation Analysis of Peripheral Blood Cells from Siblings Discordant for ASD
Case-Control
2013-05-10
phs000620
Minnesota Center for Twin and Family Research (MCTFR) Genome-Wide Association Study of Behavioral Disinhibition
Longitudinal
2013-05-17
phs000621
Genome Wide Association Studies in ECOG 2997 Trial
Clinical Trial
2013-05-17
phs000622
FaceBase Study of Facial Shape in Tanzania: CIDR
Clinical Trial
2013-05-17
phs000623
Rare Mendelian Disease in Old Order Amish and Mennonite Patients
Case Set
2013-05-20
phs000624
The Lung Genomics Research Consortium (LGRC)
Cohort
2013-05-23
phs000625
Targeted Sequencing of GWAS Loci in Cleft Lip and Palate
Parent-Offspring Trios
2013-05-31
phs000626
CD4+ cell transcriptional profiling by RNA sequencing
Control Set
2013-06-13
phs000627
University of North Carolina at Chapel Hill (UNC) Hepatocellular Carcinoma Study by Exome Sequencing (HCCSES)
Case Set
2013-06-14
phs000628
Characterization of a Metastatic Cervical Cancer Patient and HPV18 Integration Using Next Generation Sequencing
Case Set
2013-06-14
phs000629
Genetic Epidemiology of Lung Cancer Consortium GWAS of Familial Lung Cancer
Case-Control
2013-06-25
phs000630
Exome Chip Study of NIMH Controls
Control Set
2013-06-26
phs000631
ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)
Case-Control
2013-06-26
phs000632
NHLBI GO-ESP: Family Studies (Hematological Cancers)
Family
2013-06-27
phs000633
Enrichment of Lung Microbiome with Supraglottic Taxa which is Associated with Increased Pulmonary Inflammation
Cross-Sectional
2013-06-27
phs000634
National Cancer Institute (NCI) Genome Wide Association Study (GWAS) of Lung Cancer in Never Smokers
Case-Control
2013-06-28
phs000636
Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study
Family
2013-07-12
phs000637
Methotrexate Clearance GWAS in Acute Lymphoblastic Leukemia (ALL) Patients
Cohort
2013-07-22
phs000638
Genome-Wide Association Study of Relapse of Childhood Acute Lymphoblastic Leukemia
Cohort
2013-07-22
phs000639
Human Autism Genetics
Case-Control
2023-04-06
phs000640
HeLa Cell Genome Sequencing Studies
Whole Genome Sequencing
2020-10-13
phs000641
Whole Exome Sequencing Identifies
Family
2013-07-23
phs000644
The Effect of the Menstrual Cycle on DNA Expression in the Normal Human Breast Epithelium
Observational
2013-07-25
phs000645
Location and Function of NSun2-Mediated Cytosine-5 Methylation in RNA and its Effect on Translation
Case-Control
2019-03-21
phs000646
Breakpoint detection using long insert whole genome sequencing
Case Set
2013-08-02
phs000647
Study of Adaptation to Hypoxia in Ethiopian Highlanders via Whole Genome Sequencing
Cohort
2013-08-05
phs000648
Pancreatic Cancer Case Control Association Study
Case-Control
2013-08-06
phs000649
Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR and PEAR-2)
Prospective
2016-10-13
phs000650
Pediatric Investigation of Genetic Factors Linked with Renal Progression (PediGFR): Chronic Kidney Disease in Children Cohort (CKiD)
Cohort
2013-08-12
phs000652
Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Cohort
2013-08-13
phs000653
Epi4K: Gene Discovery in 4,000 Epilepsy Genomes
Parent-Offspring Trios
2016-08-03
phs000655
Genetics of Inherited Muscle Disease
Probands
2016-01-15
phs000656
Genetic measurement of memory B-cell recall using antibody repertoire sequencing
Longitudinal
2013-08-23
phs000657
A Pilot Study Using Next Generation Sequencing in Advanced Cancers: Feasibility and Challenges
Case Set
2013-08-26
phs000658
MDD2000AFFY
Case Set
2013-08-27
phs000659
Characterization of the Gut-Associated Microbiome in Inflammatory Pouch Complications Following Ileal Pouch-Anal Anastomosis
Case-Control
2013-08-29
phs000660
Chinese Alternating Hemiplegia of Childhood (AHC) Disease Study
Parent-Offspring Trios
2013-08-30
phs000661
Germline Sequencing for Aggressive Prostate Carcinoma
Case Set
2013-09-06
phs000662
National Children's Study Vanguard Study Formative Research Study (NCS)
Cohort
2013-09-11
phs000663
Drug-Induced Liver Injury Network (DILIN)
Case Set
2021-08-06
phs000664
Characterization of Autosomal CNV Among the Negrito from Peninsular Malaysia
Population
2013-09-20
phs000666
B and T Cell Determinants of Influenza Vaccine Responses in the Elderly
Longitudinal
2013-09-27
phs000669
The African American Breast Cancer Epidemiology and Risk (AMBER) Consortium Study
Case-Control
2013-09-30
phs000670
Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS)
Prospective
2013-09-30
phs000671
Somatic Mutations in Variant and IGHV4-34 Expressing Hairy Cell Leukemia
Case Set
2013-10-18
phs000672
National Institute of Dental and Craniofacial Research (NIDCR) Sjögren's International Collaborative Clinical Alliance (SICCA): Center for Inherited Disease Research (CIDR) Genome-Wide Genotyping
Multicenter
2013-10-18
phs000673
University of Michigan Clinical Sequencing Exploratory Research (CSER)
Case Set
2019-02-28
phs000674
Resource for Genetic Epidemiology Research on Adult Health and Aging (GERA)
Cohort
2013-10-23
phs000676
Sequence-Based Analysis of Human Breast Tumors
Tumor vs. Matched-Normal
2016-07-27
phs000677
An APOBEC Cytidine Deaminase Mutagenesis in Human Cancers
Meta-Analysis
2013-11-01
phs000678
The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer
Family
2013-11-05
phs000679
Genome-Wide Association Study of Anorexia Nervosa (Price Foundation, Klarman Family Foundation, Center for Applied Genomics at the Children's Hospital of Philadelphia, Scripps Translational Sciences Institute Clinical Translational Science Award)
Case-Control
2013-11-05
phs000681
Common Variation in Candidate Genes in the Diabetes Prevention Program
Clinical Trial
2018-03-20
phs000682
Genetics of Neuropsychiatric and Neurodevelopmental Disorders
Multiplex Families
2013-11-12
phs000684
Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies
Case-Control
2013-11-21
phs000687
Bulgarian Trio Sequencing Study to Identify de Novo Mutations in Schizophrenia
Parent-Offspring Trios
2013-11-26
phs000689
Genomic Analysis of Peripheral T-Cell Lymphomas
Case-Control
2013-12-12
phs000690
Whole-Genome Sequencing in Multiplex Epilepsy Families
Family
2013-12-12
phs000691
CIP: Differential Response to Hydroxyurea and Incidence of Stroke in Sickle Cell Disease
Case-Control
2014-12-02
phs000692
A Pharmcogenetic Study of Bipolar Disorder in a Taiwanese Han Chinese Population (TWBP)
Case Set
2013-12-16
phs000693
University of Washington Center for Mendelian Genomics (UW-CMG)
Mixed
2019-03-01
phs000694
Clinical Cancer Sequencing
Case Set
2017-08-07
phs000695
A Phase I/II Trial of Sirolimus (Rapamune®) and Cyclosporine in Patients with Refractory Aplastic Anemia
Clinical Trial
2014-01-06
phs000697
Mechanism and Response of Thymoglobulin in Patients with Myelodysplastic Syndrome (MDS)
Clinical Trial
2014-01-07
phs000698
QUANTitative Chest Computed Tomography UnMasking Emphysema Progression in Alpha-1 Antitrypsin Deficiency
Clinical Trial
2014-01-07
phs000699
Osteosarcoma Genomics
Case Set
2014-01-07
phs000700
NIH Roadmap Epigenomics Program - Broad Institute
Epigenetics
2019-09-24
phs000701
Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome
Prospective
2014-01-07
phs000703
CATHeterization GENetics (CATHGEN)
Longitudinal
2014-01-13
phs000706
Genome Sequencing Reveals That RAD50 Hypomorphism Results in Enhanced Sensitivity to Checkpoint Kinase Inhibition Combined with Chemotherapy
Case Set
2014-01-22
phs000707
Next Generation Mendelian Genetics: Hereditary Neurological Disorders
Case Set
2016-11-04
phs000708
Warfarin Pharmacogenetics: Pharmacogenetic Optimization of Anticoagulant Response (POAT) and Genetic and Environmental Determinants of Warfarin Response (GEDWR)
Cohort
2014-01-24
phs000709
Genomic and Transcriptomic Landscape of Fibrolamellar Hepatocellular Carcinoma
Cohort
2014-01-27
phs000710
1000 Genomes Used for Cloud Testing
Reference Set
2014-02-05
phs000711
Baylor Hopkins Center for Mendelian Genomics (BH CMG)
Mixed
2020-12-21
phs000712
University of Illinois at Chicago (UIC) Autism Centers of Excellence (ACE) Exome Sequencing Analysis
Parent-Offspring Trios
2014-02-11
phs000713
Glial Cell Line-Derived Neurotrophic Factor (GDNF) Polymorphisms and Anxiety, Depression
Cross-Sectional
2014-02-12
phs000714
NICHD Genomic and Proteomic Network for Preterm Birth Research (GPN)
Case-Control
2014-02-12
phs000715
NINDS Deep Sequencing for the Detection of Viral Sequences in Primary Progressive Multiple Sclerosis Brains
Case-Control
2014-02-14
phs000716
Genome-Wide Association Study of Lung Cancer Susceptibility in Never-Smoking Women in Asia
Case-Control
2014-02-14
phs000717
Genomics of Circulating Tumor Cells
Case Set
2014-02-14
phs000718
Trisomy21: Risk Factors for Chromosome Nondisjunction (T21NDJ)
Parent-Offspring Trios
2014-02-17
phs000719
Genetic Basis of Pulmonary Non-tuberculous Mycobacterial Infections
Family
2014-02-17
phs000720
Genomic sequencing of Pediatric Rhabdomyosarcoma
Case Set
2021-03-16
phs000721
NIH Undiagnosed Diseases Program (UDP) Genotypic and Phenotypic Study
Parent-Offspring
2014-02-21
phs000722
Whole Exome Sequencing of Colorectal Cancer Patients from the Nurses' Health Study (NHS) and Health Professionals Follow-up Study (HPFS)
Case Set
2020-10-08
phs000723
Sequencing of Cervical Cancer
Case-Control
2014-03-05
phs000725
Rare Cancer Tumors Project
Cohort
2017-01-24
phs000726
Genome-wide Association Study of Myasthenia Gravis
Case-Control
2014-03-12
phs000727
Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer's or Parkinson's disease correlate with disease status and features of pathology
Case-Control
2014-03-17
phs000728
The Genetics of Lung Cancer Susceptibility in Smokers
Family
2014-03-18
phs000729
Solution-based exome capture and HiSeq2000-based massively parallel sequencing of Follicular Lymphoma
Case Set
2014-03-18
phs000730
Genomics of Brain Metastases
Case Set
2014-03-19
phs000732
L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population
Cohort
2014-03-25
phs000733
The International Consortium for Prostate Cancer Genetics Genome Wide Association Study of Familial Prostate Cancer
Case-Control
2014-03-27
phs000734
A Genome-wide Association Study (GWAS) of Risk for Osteosarcoma
Case Set
2014-04-01
phs000735
The Placenta Harbors a Unique Microbiome
Case-Cohort
2014-04-07
phs000737
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Genetics of Genetic Epidemiology of Metabolic Syndrome in an Island Population
Cross-Sectional
2014-04-16
phs000738
Exome Sequencing in Schizophrenia Families
Parent-Offspring Trios
2014-04-17
phs000739
Identification of Recurrent SMO and BRAF Mutations in Ameloblastomas
Cohort
2014-04-17
phs000740
Whole Genome Sequencing of Waldenstrom's Macroglobulinemia
Case-Control
2014-04-21
phs000741
Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Lipidomics Study
Longitudinal
2015-10-27
phs000742
The Epilepsy Phenome/Genome Project
Parent-Offspring Trios
2014-04-30
phs000743
METSIM (METabolic Syndrome In Men) Study
Cohort
2017-02-07
phs000744
Yale Center for Mendelian Genomics (YCMG)
Mixed
2021-06-16
phs000745
ADCC Pilot RNAseq Study on Posterior Cingulate Astrocytes in Alzheimer's Disease
Case-Control
2014-05-07
phs000747
Whole Exome and Transcriptome Sequencing in Sporadic ALS
Case-Control
2017-05-12
phs000748
Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile
Longitudinal
2018-12-31
phs000750
Genomic Origins and Admixture in Latinos (GOAL)
Parent-Offspring Trios
2014-05-23
phs000751
GWAS in Fibrosing Interstitial Lung Disease
Case-Control
2014-05-23
phs000753
High Density SNP Association Analysis of Lung Cancer
Case-Control
2014-05-29
phs000755
BrainSpan Atlas of the Human Brain
Control Set
2018-11-14
phs000756
Exome Sequencing to Identify Medically Relevant Associations in Finnish Sub-Isolate Samples from the FINRISK Cohort
Longitudinal
2014-06-06
phs000757
Ataxia Gene Identification by Integrated Genomic Analysis
Family
2014-06-10
phs000758
Family Genomics of Congenital Heart Defects
Family
2014-06-11
phs000759
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Tumor vs. Matched-Normal
2014-06-12
phs000760
Human Responses to Influenza Vaccination
Case-Control
2014-06-16
phs000761
Orofacial Pain: Prospective Evaluation and Risk Assessment (OPPERA)
Case-Control
2014-06-20
phs000763
The Collaborative Study on the Genetics of Alcoholism (COGA)
Family
2014-06-20
phs000766
GEI Studies - Psoriasis
Case-Control
2014-06-25
phs000767
The UC San Diego Chronic Lymphocytic Leukemia (CLL) Study
Tumor vs. Matched-Normal
2014-06-25
phs000768
Genomic sequencing of Ewing's Sarcoma
Case Set
2016-10-03
phs000769
National Heart, Lung, and Blood Institute (NHLBI) Data Coordinating Center, Microbiome of the Lung and Respiratory Track, Lung HIV Microbiome Project (LHMP)
Observational
2014-06-26
phs000770
Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer
Cohort
2014-06-30
phs000771
Bladder Chemotherapy Responders
Case-Control
2017-10-24
phs000772
Genetic Predictors of Adverse Radiotherapy Effects (Gene-PARE)
Cohort
2014-06-30
phs000774
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes
Parent-Offspring
2017-10-17
phs000775
Transcriptome study of differential expression in schizophrenia
Case-Control
2014-07-07
phs000776
Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency
Case-Control
2014-07-09
phs000777
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis (FSGS)
Case Set
2014-07-11
phs000778
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): Identification of VUR genes by exome sequencing
Case Set
2014-07-17
phs000779
Ontario Familial Colon Cancer Registry Single Nucleotide Polymorphisms and CpG Methylation (OFCCR SNP-CpG)
Case-Control
2014-07-22
phs000781
Children's Hospital of Philadelphia: GWAS of Left-Sided Cardiac Defects
Parent-Offspring Trios
2014-07-29
phs000782
Post-liver transplant recurrent human hepatocellular carcinoma study (RHCCS)
Longitudinal
2014-07-30
phs000783
Whole Exome Sequencing of Congenital Diaphragmatic Hernia Patients and Trios
Case Set
2017-03-17
phs000784
Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Family
2019-11-15
phs000785
Exome Sequencing Analysis of Cutaneous Squamous Cell Carcinoma
Cohort
2014-08-13
phs000787
Immunosenescence: Immunity in the Young and Aged
Cohort
2014-08-14
phs000788
Research Program on Genes, Environment and Health (RPGEH)
Cohort
2017-10-16
phs000789
Collaborative Study of Genes, Nutrients and Metabolites (CSGNM)
Control Set
2014-08-18
phs000790
Comparative Sequence Analysis Between Primary and Metastatic Colorectal Cancer Lesions
Cohort
2014-08-20
phs000791
Integrated Epigenetic Maps of Human Embryonic, Extraembryonic and Adult Cells
Control Set
2019-12-10
phs000792
Oncogenomics of Malignant Peripheral Nerve Sheath Tumors
Case Set
2014-08-25
phs000793
Paired Acute Myeloid Leukemia (AML) Epigenetics Study on Epialleles and Clonality
Cohort
2014-08-27
phs000794
Longitudinal genome-wide analysis of progressive chronic lymphocytic leukemia under uniform front-line therapy of pentostatin, cyclophosphamide, and rituximab
Longitudinal
2014-09-03
phs000795
Gastric Cancer Genetic Analysis of Metastasis
Case-Control
2014-09-03
phs000796
Genome Wide Association Study of Chronic TMD: Discovery Phase
Case-Control
2014-09-03
phs000797
Immune Dysregulation in Human Subjects with Heterozygous Germline Mutations in
Case Set
2014-09-03
phs000798
Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing
Control Set
2014-09-05
phs000799
Shanghai Breast Cancer Genetics Study (SBCGS)
Case-Control
2014-09-11
phs000801
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Cohort
2016-01-05
phs000803
Gastrointestinal Cancer Treatment Responders
Longitudinal
2016-11-14
phs000804
Genomic Sequencing of Ewing Sarcoma
Whole Genome Sequencing
2014-09-23
phs000806
Myocardial Infarction Genetics Exome Sequencing Consortium: Ottawa Heart Study
Case-Control
2014-09-26
phs000807
Study on longer adjuvant chemotherapy in Women with Early Breast Cancer
Cohort
2014-09-29
phs000808
PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS)
Case-Control
2014-10-01
phs000809
Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment
Parent-Offspring Trios
2014-10-01
phs000810
Hispanic Community Health Study /Study of Latinos (HCHS/SOL)
Cohort
2014-10-03
phs000811
Comparison of Custom Capture for Targeted Next Generation DNA Sequencing
Mixed
2014-10-03
phs000812
The Breast and Prostate Cancer Cohort Consortium (BPC3) GWAS of Aggressive Prostate Cancer and ER- Breast Cancer
Case-Control
2014-10-06
phs000813
CIDR, NCI, NIDA Sequencing of Targeted Genomic Regions Associated with Smoking
Case-Control
2014-10-07
phs000814
Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology
Case-Control
2014-10-08
phs000815
Gene Expression and Regulatory Networks in Human Leukocytes - Immunological Variation Consortium
Control Set
2020-01-30
phs000816
Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing
Parent-Offspring Trios
2016-04-19
phs000817
Responses to Varicella Zoster Virus Vaccination
Cohort
2014-10-16
phs000819
The Normal Human Tissue Sequencing Project: Non-Diseased, Non-Malignant Tissues
Control Set
2014-10-17
phs000820
The Cleveland Clinic Foundation's (CCF) Lone Atrial Fibrillation (AFIB) GWAS Study
Case Set
2023-01-11
phs000821
DNA Methylation age and mortality in the Lothian Birth Cohorts of 1921 and 1936
Longitudinal Cohort
2014-10-21
phs000822
Genome-Wide Discovery of Novel Breast Cancer Predisposing Mutations
Case Set
2014-10-21
phs000823
Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing
Case Set
2014-10-22
phs000824
Genome-Wide Discovery of Novel Colon Cancer Predisposing Mutations
Case Set
2014-10-22
phs000825
Whole Genome Sequencing of Harvard University Embryonic Stem Cell Lines 63 and 64
Control Set
2014-10-24
phs000826
Prediction of Trastuzumab Benefit in Adjuvant Breast Cancer: Gene Expression Profiling in NSABP B31
Clinical Trial
2014-10-28
phs000827
North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)
Case Set
2016-09-01
phs000828
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Case Set
2014-11-04
phs000830
Xeroderma Pigmentosum, Complementation Group C, (XPC) and Non-XPC Cutaneous Squamous Cell Carcinoma (cSCC) Mutation Rate Study
Cohort
2014-11-06
phs000831
Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Parent-Offspring Trios
2014-11-13
phs000832
Sensitivity to the Subjective Effects of Amphetamine
Cohort
2014-11-13
phs000833
Single Cell Analysis Program - Transcriptome (SCAP-T)
Case Set
2017-08-04
phs000837
Whole Genome Sequencing of Two Family Trios with 22q.11.2 Deletion Syndrome
Parent-Offspring Trios
2014-11-17
phs000838
Ghana Prostate Study
Case-Control
2014-11-17
phs000839
Efficacy of Bitter Taste Blockers on Flavor Acceptance in a Human Population
Control Set
2014-11-18
phs000840
The Genetics of Type 2 Diabetes Consortium (GoT2D): Low-Pass Sequencing and High-Density SNP Genotyping for Type 2 Diabetes
Case-Control
2014-11-21
phs000841
Sanger sequencing of catalytic-domain encoding exons of tyrosine kinase genes from human endometrial tumor DNAs
Case Set
2014-11-26
phs000842
Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)
Cohort
2017-10-16
phs000845
Genomic Factors Involved in Chromosome Rearrangements
Cohort
2014-12-01
phs000846
Whole Genome Bisulfite Sequencing of Circulating Cell-Free (CCF) DNA and its Cellular Contributors
Cross-Sectional
2014-12-02
phs000847
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Family
2016-08-04
phs000848
Autosomal recessive
Case-Control
2014-12-03
phs000851
African American Breast Cancer GWAS
Case-Control
2015-01-05
phs000852
GEDI: A Developmental Model of Gene-Environment Interplay in SUDs: Combined Genotype Dataset from the "Great Smoky Mountains Study" and the "Caring for Children in the Community Study".
Case-Control
2015-01-05
phs000853
Normative Aging Study (NAS)
Longitudinal Cohort
2022-01-27
phs000855
Resistance studies in Lung Cancer
Case-Control
2015-01-08
phs000856
Chromothripsis in Patient WHIM-09
Single Patient
2015-01-12
phs000857
Primary ER-positive Breast Cancer Treated with Neoadjuvant Letrozole
Clinical Trial
2015-01-13
phs000858
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
Parent-Offspring Trios
2015-01-14
phs000862
Lysosomal Disease Network (LDN6719) Immune Response to Intrathecal Enzyme Therapy in Mucopolysaccharidosis 1 Patients
Observational
2015-01-27
phs000863
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Case-Control
2015-01-27
phs000864
Genomic Predictors of Combat Stress Vulnerability and Resilience
Longitudinal Cohort
2015-02-02
phs000866
Family Genomics of Bipolar Disorder
Family
2015-02-04
phs000867
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study
Case-Control
2015-02-06
phs000868
Transcriptome Sequencing of Pediatric Neuroblastoma
Case Set
2015-02-10
phs000869
Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
Case-Control
2015-02-11
phs000870
Characterization of Human Transcriptome by Computational and HTS Approaches
Control Set
2015-02-20
phs000871
Whole Exome Sequencing of Pancreatic Neuroendocrine Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Cohort
2015-02-24
phs000872
Autism Post-Mortem Brain RNA-Sequencing: SRRM4 Splicing Study
Case-Control
2015-02-24
phs000873
Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition
Family
2015-02-25
phs000874
Genetic and Environmental Risk Factors for Hemorrhagic Stroke (GERFHS)
Case-Control
2015-02-26
phs000876
Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing
Case-Control
2018-09-05
phs000879
Dana-Farber Cancer Institute (DFCI) Brown Lab CLL Sequencing Study
Cohort
2020-06-30
phs000882
National Cancer Institute (NCI) Prostate Cancer Genome-Wide Association Study for Uncommon Susceptibility Loci (PEGASUS)
Case-Control
2015-03-09
phs000883
Myocardial Infarction Genetics Exome Sequencing Consortium: Precocious Coronary Artery Disease Study
Case-Control
2015-03-12
phs000884
Gut microbiome profiles according to sex, body mass index and dietary fiber intake
Control Set
2015-03-17
phs000885
CAGE Profiling of ncRNAs in Hepatocellular Carcinoma Reveals a Strong Activation of Retroviral LTR Promoters in Virus-Induced Tumors
Case-Control
2015-03-18
phs000886
An Omics View of Asthma through Monozygotic Twins
Case-Control
2015-03-18
phs000888
eMERGE Network Imputed GWAS for 41 Phenotypes
Case-Control
2015-03-19
phs000892
Clinical Proteomic Tumor Analysis Consortium (CPTAC) Proteogenomic Confirmatory Study of Breast, Colon, Lung, and Ovarian Tumors
Case Set
2017-02-07
phs000893
Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2)
Case-Control
2015-03-27
phs000894
Genome Wide Association Study of Serum Creatinine during Vancomycin Therapy and Vancomycin Pharmacokinetics
Cohort
2015-03-31
phs000895
Integrated Genomic Analysis of Periampullary Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Cohort
2015-04-01
phs000896
Functional Dynamics of the Elderly Gut Microbiome During Probiotic Consumption
Longitudinal
2015-04-02
phs000897
Mayo Clinic and Illumina Collaborative Early Stage Ovarian Cancer (ESOC) Study
Case Set
2015-04-03
phs000898
Megabase-scale Haplotyped Genomic Analysis of Normal and Cancer Genomes
Case Set
2022-12-13
phs000899
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Family
2015-04-07
phs000900
Functionally-defined Therapeutic Targets in Diffuse Intrinsic Pontine Glioma (DIPG)
Cohort
2015-04-09
phs000901
University of Washington Cerebrospinal Fluid Biomarker Study for Parkinson disease
Case-Control
2015-04-17
phs000902
Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor
Case-Control
2015-04-20
phs000903
OCD Collaborative Genetic Association Study (OCGAS)
Parent-Offspring Trios
2015-04-22
phs000904
Novel APC Promoter and Exon 1B Deletion and Allelic Silencing in Three Mutation-Negative Classic Familial Adenomatous Polyposis Families
Mendelian
2015-04-22
phs000906
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Cohort
2015-04-27
phs000907
Next Generation Sequencing of Stage IV Squamous Cell Lung Cancers Reveals an Association of PI3K Aberrations and Evidence of Clonal Heterogeneity in Patients with Brain Metastases
Case Set
2015-04-28
phs000908
University of Miami Udall Center of Excellence Identification of Rare Variants in PD through Whole Exome Sequencing
Case-Control
2015-04-30
phs000909
Molecular Basis of Neuroendocrine Prostate Cancer (Trento/Cornell/Broad 2015)
Cohort
2015-05-01
phs000910
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Affected Sib Pairs
2015-05-04
phs000911
Type 1 Diabetes Genetics Consortium (T1DGC): ImmunoChip Study
Case-Control
2015-05-04
phs000912
San Francisco Bay Area Latina Breast Cancer Study
Case-Control
2015-05-04
phs000913
Genomic Analysis of Mycosis Fungoides and Sézary Syndrome Identifies Recurrent Alterations in TNFR2
Tumor vs. Matched-Normal
2015-05-06
phs000914
Genome-wide Association Study of Adiposity in Samoans
Cross-Sectional
2015-05-06
phs000915
Stand Up To Cancer East Coast Prostate Cancer Research Group
Case Set
2016-04-19
phs000916
Myocardial Infarction Genetics Exome Sequencing Consortium: German Heart Center in Munich
Case-Control
2015-05-19
phs000917
Myocardial Infarction Genetics Exome Sequencing Consortium: Pakistan Risk Of Myocardial Infarction Study
Case-Control
2015-05-19
phs000918
International Parkinson's Disease Genomics Consortium (IPDGC), NeuroX Dataset
Case-Control
2015-05-19
phs000920
NHLBI TOPMed - NHGRI CCDG: Genes-Environments and Admixture in Latino Asthmatics (GALA II)
Case Set
2020-10-08
phs000921
NHLBI TOPMed: Study of African Americans, Asthma, Genes and Environment (SAGE)
Case-Control
2019-11-18
phs000922
Genetic Aberrations and Subclonal Structure Impact Chronic Lymphocytic Leukemia
Longitudinal
2021-05-14
phs000923
Molecular Characterization of Germ Cell Tumors
Cohort
2015-05-29
phs000924
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for studying the impact of genetic variation on molecular and physiological phenotypes
Control Set
2019-07-19
phs000925
PAGE: The Charles Bronfman Institute for Personalized Medicine (IPM) BioMe BioBank
Longitudinal Cohort
2015-06-01
phs000926
Rare Disease Susceptibility Alleles in Children with Crohn Disease
Family
2015-06-03
phs000927
CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen)
Randomized
2015-06-05
phs000928
Transcriptomic Profile of Whole Blood Cells from Elderly Subjects fed Probiotic Bacteria Lactobacillus rhamnosus GG ATCC 53103 (LGG) in a Phase I Open Label Study
Longitudinal
2015-06-05
phs000929
High-Risk Breast Cancer GWAS
Case-Control
2015-06-09
phs000930
CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology) Consortium Summary Results from Genomic Studies
Cohort
2022-01-02
phs000931
DMET Genes, Nicotine Metabolism and Prospective Abstinence
Family
2015-06-11
phs000932
A Somatic Reference Standard for Cancer Genome Sequencing
Tumor vs. Matched-Normal
2015-06-15
phs000933
Genomic Profiling of Melanoma
Case Set
2021-11-04
phs000934
Antibody Repertoires in CVID
Case-Control
2015-06-16
phs000935
The CHOP Pediatric Genetic Sequencing (PediSeq) Project : Applying Genomic Sequencing in Pediatrics
Cross-Sectional
2015-06-16
phs000936
NHLBI GO-ESP: Early-Onset Myocardial Infarction Exome Chip (Broad EOMI)
Case-Control
2015-06-16
phs000937
The Landscape of Antisense Gene Expression in Human Cancers
Cohort
2015-06-16
phs000938
Evaluation of Hybridization Capture versus Amplicon-based Methods for Whole Exome Sequencing
Control Set
2015-06-16
phs000939
Detection of Enhancer-Associated Rearrangements Reveals Mechanisms of Oncogene Dysregulation in B-cell Lymphoma
Case Set
2017-08-15
phs000941
Phylogenetic Analyses of Melanoma Reveal Complex Patterns of Metastatic Dissemination
Tumor vs. Matched-Normal
2015-06-23
phs000942
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
Cohort
2015-06-24
phs000944
eMERGE Phase III Clinical Center at Partners HealthCare
Cross-Sectional
2015-06-29
phs000945
Genomic Characterization of African-American Prostate Cancer
Cohort
2015-06-30
phs000946
NHLBI TOPMed: Boston Early-Onset COPD Study
Probands
2022-11-18
phs000947
Genome-Wide Assessment of DNA Methylation in Systemic Lupus Erythematosus-Related Autoantibodies
Case Set
2015-07-01
phs000948
Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II)
Cohort
2015-07-01
phs000949
Genetic Analysis of Normal Human Facial Variation
Control Set
2015-07-02
phs000950
Surveillance, Epidemiology and End Results (SEER) Formalin Fixed Paraffin Embedded (FFPE) Tissue Feasibility Study
Case Set
2015-07-06
phs000951
NHLBI TOPMed: Genetic Epidemiology of COPD (COPDGene)
Case-Control
2020-10-08
phs000952
Substance Dependence GWAS in European- and African - Americans
Case-Control
2015-07-10
phs000953
Microdissected Pancreatic Cancer Whole Exome Sequencing
Longitudinal Cohort
2015-07-10
phs000954
NHLBI TOPMed: The Cleveland Family Study (CFS)
Longitudinal
2020-10-08
phs000955
Genetic Components of Knee Osteoarthritis (GeCKO) Study: The Osteoarthritis Initiative
Longitudinal
2015-07-10
phs000956
NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish
Family
2020-10-08
phs000957
Geisinger Health System - MyCode, eMERGE III Exome Chip
Case-Control
2015-07-16
phs000958
National Human Genome Research Institute (NHGRI) Clinical Sequencing Exploratory Research (CSER) The MedSeq Project: Integration of Whole Genome Sequencing into Clinical Medicine (HG006500)
Case-Control
2015-07-18
phs000959
Exome Sequencing of Schizophrenia Cases and Controls in the South African Xhosa Population
Case-Control
2015-07-21
phs000960
Biomarkers in Transplant Recipients
Case Set
2020-02-12
phs000961
eMERGE III: Columbia GENIE (Genomic Integration with EHR)
Case-Control
2015-07-21
phs000962
Exploring the Genetic Variants Associated with Brain Growth in Children
Case Set
2015-07-22
phs000963
PGRN-RIKEN: Genetic Determinants of Clinical Cardiovascular Events in Patients Receiving Statins
Case-Control
2015-07-23
phs000964
NHLBI TOPMed: The Jackson Heart Study (JHS)
Longitudinal Cohort
2020-10-08
phs000966
National Institute of Neurological Disorders and Stroke (NINDS), Family Study of Essential Tremor (FASET), Identification of Susceptibility Genes for Essential Tremor
Multiplex Families
2023-02-16
phs000967
Exome Sequencing of Clear Cell Endometrial Tumors and Paired Non-tumor Samples
Case Set
2015-07-29
phs000968
The Cardiopulmonary Effects of Particulate Exposure
Longitudinal
2019-11-05
phs000969
Whole Exome Sequencing of One Nuclear Family with Non-syndromic Sensorineural Hearing Loss
Parent-Offspring
2015-08-03
phs000970
The Influence of Gut Microbiota on the Speciation and Toxicity of Mercury During Pregnancy
Cross-Sectional
2015-08-04
phs000971
The ClinSeq Project: Piloting Large-Scale Genome Sequencing for Research in Genomic Medicine
Case Set
2021-05-27
phs000972
NHLBI TOPMed: Genome-Wide Association Study of Adiposity in Samoans
Cross-Sectional
2020-10-08
phs000973
The Genomic Landscape of Juvenile Myelomonocytic Leukemia
Collection
2015-08-10
phs000974
NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study
Cohort
2020-10-08
phs000975
The Nurses' Health Study (NHS) GWAS of Mammographic Density
Case-Control
2015-08-13
phs000976
Study on the Genetics of Alcoholism (COGA): African American Family GWAS
Family
2020-08-24
phs000977
Genetic Analysis of Desmoplastic Melanoma
Tumor vs. Matched-Normal
2015-08-19
phs000978
Whole-Genome Sequencing (WGS) of a Malignant Granular Cell Tumor (GCT) with Metabolic Response to Pazopanib
Case-Control
2015-08-21
phs000979
HBCC Postmortem Psychiatric Molecular Studies
Case-Control
2019-09-06
phs000980
Mutational Landscape Determines Sensitivity to PD-1 Blockade in Non-Small Cell Lung Cancer
Cohort
2015-08-25
phs000981
Lactobacillus rhamnosus GG ATCC (LGG) as an immune adjuvant for influenza vaccination in the elderly
Longitudinal
2015-08-26
phs000982
Genetic Analysis of Psoriasis and Psoriatic Arthritis: GWAS of Psoriatic Arthritis
Case-Control
2015-09-01
phs000983
Pharmacogenomics of Rheumatoid Arthritis Therapy
Case Set
2015-09-01
phs000984
Pharmacogenomics of Metformin Dose Response in T2DM Patients
Case Set
2015-09-01
phs000985
Functional Significance of Prostate Cancer Risk-SNPs
Cohort
2022-02-16
phs000986
Genetic Basis of Cryptorchidism
Case-Control
2015-09-04
phs000987
Whole exome sequencing of 184 unrelated subjects with 22q11.2 deletion syndrome (DiGeorge syndrome/velo-cardio-facial syndrome)
Case Set
2015-09-08
phs000988
NHLBI TOPMed: The Genetic Epidemiology of Asthma in Costa Rica
Parent-Offspring Trios
2020-10-08
phs000989
Cellular Diversity of the Developing Human Cerebral Cortex
Cohort
2023-05-22
phs000990
Myocardial Infarction Genetics Exome Sequencing Consortium: University of Lubeck
Case-Control
2015-09-18
phs000991
VESPA: Vanderbilt Electronic Systems for Pharmacogenomic Assessment
Cohort
2015-09-22
phs000993
NHLBI TOPMed: Heart and Vascular Health Study (HVH)
Case Set
2021-05-10
phs000994
The Mutational Landscape of CTCL and Sezary Syndrome
Longitudinal Cohort
2015-09-24
phs000996
Genome-Wide Environment Interaction Study on Neurodevelopment in Children from Mexico and Bangladesh
Cohort
2019-08-13
phs000997
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt AF Ablation Registry
Case Set
2021-05-10
phs000998
RNA Sequencing of Pulmonary Arterial Endothelial Cells in Pulmonary Hypertensive Patients and Controls
Case-Control
2016-05-02
phs000999
Clinical Sequencing Exploratory Research (CSER): Clinical sequencing in cancer: Clinical, ethical, and technological studies
Longitudinal
2019-11-22
phs001000
Myocardial Infarction Genetics Exome Sequencing Consortium: U. of Leicester
Case-Control
2015-10-01
phs001001
Massachusetts General Hospital (MGH) Atrial Fibrillation Study
Case Set
2015-10-01
phs001002
A Genome-Wide Association Study of CALGB 90401: Randomized, Double-Blind, Placebo-Controlled Phase III Trial Comparing Docetaxel and Prednisone with or without Bevacizumab in Men with Metastatic Castration-Resistant Prostate Cancer
Cohort
2015-10-08
phs001003
Prospective Procurement of Solid Tumor Tissue to Identify Novel Therapeutic Targets
Cohort
2022-02-24
phs001004
Genetic Analysis of Parkinson's Disease
Parent-Offspring Trios
2015-10-14
phs001005
Identification of Putative Neoantigens in Stage III Melanoma
Case Set
2016-01-04
phs001006
Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease
Prospective
2015-10-15
phs001007
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Case Set
2015-10-20
phs001008
GUARDIAN: The Insulin Resistance Atherosclerosis Family Study (IRASFS)
Family
2015-10-20
phs001009
Determinants of Asthma Following RSV Bronchiolitis in Early Life
Prospective
2015-10-22
phs001011
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Cohort
2020-07-21
phs001012
The Diabetes Heart Study (DHS)
Cross-Sectional
2015-10-27
phs001013
Heart and Vascular Health Study (HVH)
Case-Control
2017-08-21
phs001014
GUARDIAN: The Insulin Resistance Atherosclerosis Study (IRAS Classic)
Cohort
2015-10-27
phs001015
Genome Wide Association Study of Subjects with Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)
Case-Control
2015-10-27
phs001016
Fixed single-cell transcriptomic characterization of human radial glial diversity
Single Cell Analysis
2015-10-28
phs001017
Breast Cancer Susceptibility
Case Set
2015-10-28
phs001018
Molecular Characterization of Clinical Renal Tumors
Cohort
2015-10-28
phs001020
Genomic Psychiatry Cohort (GPC) Whole Genome Sequencing and Genotyping Study
Case-Control
2019-08-08
phs001021
CHDWB Rare Regulatory Alleles and Gene Expression Study
Cohort
2015-10-29
phs001022
PsychENCODE Consortium: Epigenetic and Transcriptional Dysregulation in Autism Spectrum
Case-Control
2015-10-29
phs001023
Male Infertility: Genetics of Spermatogenic Failure
Case-Control
2015-10-29
phs001024
NHLBI TOPMed: Partners HealthCare Biobank
Case Set
2021-05-10
phs001025
GWAS in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture
Case-Control
2015-11-02
phs001026
Baylor College of Medicine Advancing Sequencing in Childhood Cancer Care (BASIC3) Clinical Exome Sequencing Study - Clinical Sequencing Exploratory Research Consortium
Longitudinal
2015-11-02
phs001027
Epigenomics Studies in Acute Myeloid Leukemia (AML)
Cohort
2021-06-09
phs001028
Complete Genomics Deep Whole-Genome Sequencing of Circulating Tumor Cells from a Patient with Metastatic Breast Cancer
Case Set
2015-11-06
phs001030
Viral Respiratory Pathogens Genetics
Cohort
2015-11-09
phs001032
NHLBI TOPMed: The Vanderbilt Atrial Fibrillation Registry (VU_AF)
Case Set
2021-05-11
phs001033
PAGE: Global Reference Panel
Control Set
2015-11-16
phs001034
New England-Based Case-Control Study of Ovarian Cancer
Case-Control
2015-11-17
phs001036
Comprehensive Genomic Characterization of Acral Melanoma
Tumor vs. Matched-Normal
2015-11-24
phs001037
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Longitudinal
2015-11-25
phs001038
Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses
Case Set
2015-12-03
phs001039
International Age-Related Macular Degeneration Genomics Consortium - Exome Chip Experiment
Case-Control
2015-12-03
phs001040
NHLBI TOPMed: Novel Risk Factors for the Development of Atrial Fibrillation in Women
Case Set
2022-11-16
phs001041
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Longitudinal Cohort
2015-12-14
phs001043
A Genome-Wide Association Study in Patients Experiencing Breast Events While Receiving Adjuvant Aromatase Inhibitors for Early Breast Cancer on NCIC CTG Trial MA.27
Case-Control
2015-12-15
phs001044
Breast Cancer Risk Pathways
Case-Control
2015-12-17
phs001045
Molecular Epidemiology of Colorectal Cancer (MECC) Metastasis Study: A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis
Case Set
2015-12-17
phs001046
Genomic Architecture of Progression and Treatment Response in AMD
Case-Control
2015-12-18
phs001048
The Finland-United States Investigation of NIDDM Genetics (FUSION) Tissue Biopsy Study
Cohort
2018-12-31
phs001049
Genomics of Relapsed Small Cell Lung Cancer Progression
Case Set
2015-12-22
phs001050
Breast Cancer Genome Guided Therapy Study (BEAUTY)
Case Set
2015-12-22
phs001052
Modelling Multi-Dimensional ClinOmics for Precision Therapy of Children and Adolescent Young Adults with Relapsed and Refractory Cancer: A report from the Center for Cancer Research.
Cohort
2019-12-13
phs001053
National Eye Institute (NEI) Exfoliation Genotyping Study
Case Set
2015-12-23
phs001054
Genomic Characterization of Pediatric Low-Grade Gliomas
Case Set
2015-12-28
phs001055
Whole Genome Study for De Novo Mutation Rates
Parent-Offspring Trios
2015-12-30
phs001057
Population Genetics Analysis Program: Immunity to Vaccines/Infections - Smallpox Vaccination (NIAID/NIH)
Cohort
2016-01-05
phs001058
Myocardial Infarction Genetics Exome Sequencing Consortium: BioImage Study
Case-Control
2016-01-06
phs001059
Maternal Plasma Folate and DNA Methylation in Epigenome-Wide Meta-Analysis of Newborns
Longitudinal
2016-01-13
phs001062
NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study
Case Set
2021-05-11
phs001063
Genomic Characterization of Patient-Derived Xenograft Models to Improve Targeted Therapy for HER2+ Breast Cancer Brain Metastases Treatments
Case Set
2016-01-29
phs001064
Whole Exome Sequencing of Six Signet Ring/Plasmacytoid Variant Bladder Tumors
Cohort
2016-01-29
phs001065
Coenzyme Q10 (CoQ) in Huntington's Disease (HD) (2CARE)
Multicenter
2016-01-29
phs001066
Whole Genome, Exome, Transcriptome and Validation Sequencing of an Acute Lymphoblastic Leukemia
Case Set
2016-01-29
phs001067
Metagenomic Deep Sequencing in Meningitis and Encephalitis
Case Set
2016-02-01
phs001071
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Case-Control
2016-02-10
phs001072
Mechanisms of Therapy Driven Clonal Evolution in Oncogenic RAS Mutant Relapsed Acute Lymphoblastic Leukemia
Cohort
2016-02-12
phs001073
Epigenetic Analysis of Malnutrition
Clinical Trial
2022-01-31
phs001074
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Longitudinal Cohort
2016-02-22
phs001075
Sequencing to Guide Cancer Care (CanSeq)
Case Set
2016-02-23
phs001076
Inflammatory Bowel Disease Exome Sequencing Study
Case Set
2016-02-23
phs001078
Common Variant GWAS, Genetics & Epidemiology of Colorectal Cancer Consortium (GECCO)
Case-Control
2016-02-26
phs001079
Transcriptional Profiling of PD-1+ and PD-1- Teff and Treg Cells in Glioblastoma and Health
Case-Control
2017-08-24
phs001080
Genome Studies in Hereditary Spastic Paraplegia
Case Set
2016-03-01
phs001082
Zostavax vaccination-induced changes in the T cell receptor repertoire to varicella zoster virus
Longitudinal
2016-03-02
phs001083
99 Cases of Small Cell Lung Cancer Study
Case Set
2016-03-02
phs001084
Differential Mutations in Matched Primary and Metastatic Colorectal Cancers
Case Set
2016-03-04
phs001085
Genetic History of Neandertal and Denisovan Introgression into Melanesian Individuals
Population
2016-03-04
phs001087
Common deleterious germline variants shape the urothelial cancer genome
Case Set
2020-02-11
phs001088
Shanghai Breast Cancer Genetics Study (SBCGS)
Case-Control
2016-03-14
phs001089
HudsonAlpha Institute for Biotechnology Clinical Sequencing Exploratory Research (CSER): Genomic Diagnosis in Children with Developmental Delay
Family
2021-01-19
phs001090
Genome-wide Association Study for Non-syndromic Clefts in the African Population: CIDR
Case-Control
2016-03-18
phs001091
Clonal Evolution in Patients with Chronic Lymphocytic Leukemia
Longitudinal
2016-03-18
phs001093
Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: London Life Sciences Population Study (LOLIPOP) UK South Asian
Case-Control
2016-03-25
phs001095
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Ashkenazi
Case-Control
2016-03-28
phs001096
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: KARE
Case-Control
2016-03-28
phs001097
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Singapore
Case-Control
2016-03-28
phs001101
Myocardial Infarction Genetics Exome Sequencing Consortium: Malmo Diet and Cancer Study
Case-Control
2016-03-29
phs001105
NHGRI-Mayo Clinic Whole Genome Sequencing of Aggressive Prostate Tumors
Case-Control
2016-04-07
phs001106
Genomics of Hepatocellular Carcinoma
Case Set
2016-04-08
phs001107
Patient-Specific Factors Influence Somatic Variation Patterns in Von Hippel-Lindau Disease Renal Tumors
Tumor vs. Matched-Normal
2016-04-11
phs001108
Assessing Neural Mechanisms of Injury in Inborn Errors of Urea Metabolism Using Structural MRI, Functional MRI, and Magnetic Resonance Spectroscopy
Case-Control
2016-04-13
phs001109
Addictions: Genotypes, Polymorphisms, and Function/Human Genetic Correlates of Addictive Diseases
Case-Control
2020-02-25
phs001110
Kids First: Pediatric Research Project on the Genomic Analysis of Congenital Diaphragmatic Hernia
Parent-Offspring Trios
2020-08-26
phs001111
A Multi-Gene Mutation Classification of 468 Colorectal Cancers Reveals a Prognostic Role for APC
Case Set
2016-04-22
phs001112
Chromosome X Mosaicism Methylation Study
Case Set
2016-05-03
phs001115
Melanoma and Cancer-Associated Fibroblast Short-Term Cultures Derived from Patient Metastases
Case Set
2016-05-03
phs001119
Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS)
Longitudinal Cohort
2016-05-10
phs001120
ELLIPSE Prostate Cancer Meta-Analysis and Genotyping
Case-Control
2020-12-08
phs001121
Integrated Genetic and Pharmacologic Interrogation of Rare Cancers
Cohort
2016-05-13
phs001122
Genome-wide Identification of Variants Affecting Early Human Brain Development
Cohort
2016-05-16
phs001123
Consortium on Asthma among African-ancestry Populations in the Americas (CAAPA)
Population Genomics
2019-02-21
phs001124
Mechanisms of Risk for Sulfonamide Hypersensitivity
Case-Control
2016-05-18
phs001127
Genomic Analysis of Paired Endometrial Cancer Primaries and Metastases
Case Set
2016-05-20
phs001130
NIDDM-Atherosclerosis Study (NIDDM-Athero)
Cohort
2016-05-23
phs001133
Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Case-Control
2016-05-24
phs001134
Radiation-Related Genomic Profile of Papillary Thyroid Cancer after the Chernobyl Accident
Case Set
2022-10-26
phs001135
Starting Treatment with Agonist Replacement Therapies (START): A Randomized Trial of Methadone vs Buprenorphine/Naloxone for the Treatment of Opioid Dependence
Longitudinal
2020-02-27
phs001138
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Gabriella Miller Kids First Pediatric Research Program of the Pediatric Cardiac Genetics Consortium (PCGC)
Cohort
2021-09-02
phs001139
NextGen Consortium: GENESiPS Study: Identifying the Gene Networks of Insulin Resistance
Case-Control
2016-06-07
phs001140
ALCHEMIST Study
Case Set
2016-06-07
phs001141
PROstate Cancer Medically Optimized Genome Enhanced ThErapy (PROMOTE) of Castration Resistant Prostate Cancer (CRPC) Patients Treated with Abiraterone Acetate
Case Set
2022-08-03
phs001143
NHLBI TOPMed: The Genetics and Epidemiology of Asthma in Barbados
Family
2020-10-08
phs001145
Exceptional Responders Initiative
Case-Control
2016-06-09
phs001146
Expression Quantitative Trait Locus Mapping Studies in Mid-Secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes
eQTL
2016-06-09
phs001151
Region-specific Transcriptome Analysis of the Human Retina and Retinal Pigment Epithelium (RPE)/Choroid
Control Set
2016-06-14
phs001152
Somatic Mutational Analysis by Exome Sequencing Endometrial Carcinosarcomas
Case Set
2016-06-16
phs001153
Somatic Mutational Analysis by Exome Sequencing Late-Stage Endometrioid Endometrial Carcinoma
Case Set
2016-06-16
phs001154
Indexing Genes Impacted by Copy Number Variation in Developmental Disorders
Case-Control
2016-06-16
phs001156
The EVE Asthma Genetics Consortium: Building Upon GWAS
Case-Control
2017-08-21
phs001157
Wisconsin Longitudinal Study on Aging
Longitudinal Cohort
2016-06-21
phs001158
Human Dorsal Root Ganglion RNA Landscape Profiling for Neuropathic and Chronic Pain
Case-Control
2019-01-31
phs001159
Genomic Profiling of Sequentially Acquired Metastatic Sites from an "Exceptional Responder" Lung Adenocarcinoma Patient Reveals Extensive Genomic Heterogeneity and Novel Somatic Variants
Case Set
2016-06-22
phs001163
CRU-Ukrainian National Research Center for Radiation Medicine Trio Study
Parent-Offspring Trios
2016-06-27
phs001164
The Role of Germline Mutation and Parental Age in Autism Spectrum Disorders
Parent-Offspring Trios
2016-06-30
phs001165
eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics
Longitudinal Cohort
2016-07-01
phs001166
Type 2 Diabetes Starr County GWAS and Exome Sequencing
Case-Control
2016-07-06
phs001167
Type 2 Diabetes in African Americans, GWAS and Exome Sequencing
Case-Control
2016-07-06
phs001168
Kids First: Genomic Studies of Orofacial Cleft Birth Defects
Parent-Offspring Trios
2019-02-26
phs001169
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Version 2)
Case Set
2020-03-31
phs001172
National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease
Case-Control
2016-07-20
phs001173
National Cancer Institute (NCI) Head and Neck Cancer Study
Case-Control
2016-07-20
phs001174
Female Infertility: Primary Ovarian Insufficiency
Case Set
2016-07-21
phs001175
CTSP: Clinical Trial Sequencing Project
Case Set
2018-12-14
phs001176
Gene-Environment Interactions (GxE) and Complex Traits
Reference Set
2019-08-27
phs001177
Rare germline sequence variants, copy number variations, expression alterations, methylation variations and disease susceptibility in familial melanoma
Family
2017-08-02
phs001178
Disorders/Differences of Sex Development (DSD) Study Performed at UCLA in Collaboration with the DSD-Translational Research Network (DSD-TRN), with the Support of the Gabriella Miller Kids First Pediatric Research Program
Parent-Offspring Trios
2016-07-27
phs001179
Foundation Medicine Adult Cancer Clinical Dataset (FM-AD)
Case Set
2016-07-29
phs001180
Genes-Environments and Admixture in Latino Asthmatics (GALA II) Study
Case-Control
2019-12-11
phs001181
Single-Cell DNA and RNA Sequencing over A 29-Year Period of A CLL Patient Demonstrating Evolution of Multiple Cell Clones
Case Set
2016-08-03
phs001182
National Institute of Environmental Health (NIEHS) Sciences Study of Somatic Mutation Load in Clones of Single Human Cells
Control Set
2020-08-24
phs001185
Genome-Wide Scan for Genetic Variants Associated with Early-Onset Prostate Cancer
Case-Control
2016-08-09
phs001187
Epigenomics of Human CD8 T cell Differentiation and Aging
Case-Control
2016-08-10
phs001188
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study - Islet Expression and Regulation by RNAseq and ATACseq
Control Set
2019-02-27
phs001189
NHLBI TOPMed: Cleveland Clinic Atrial Fibrillation (CCAF) Study
Case Set
2021-05-19
phs001191
eMERGE: Northwestern (NUgene) WGS
Longitudinal
2016-08-15
phs001192
Thoracic Patient-Derived Xenografts
Case Set
2016-08-16
phs001193
National Cancer Institute (NCI) Adding Hispanics to Ongoing GWAS in Colorectal Cancer
GWAS
2016-08-16
phs001194
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC) Study
Parent-Offspring Trios
2019-01-02
phs001195
A Study to Assess the Cardiovascular, Cognitive, and Subjective Effects of Atomoxetine in Combination with Intravenous Methamphetamine
Case-Control
2016-08-22
phs001196
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Case-Control
2016-08-23
phs001197
Neural Systems, Inhibitory Control, and Methamphetamine Dependence
Case-Control
2016-08-23
phs001198
Early Methamphetamine Abstinence: fMRI and Brain Function
Case-Control
2016-08-23
phs001199
TIGER-LC OncoVar Sequencing
Case Set
2016-08-23
phs001200
Neutralizing Antibodies against West Nile Virus Identified Directly from Human B Cells by Single-Cell Analysis and Next Generation Sequencing
Case Set
2016-08-26
phs001201
ASsessing and Predicting Infant RSV Effects and Severity (AsPIRES) Study
Longitudinal
2018-05-11
phs001202
OncoArray: Oral and Pharynx Cancer
Case-Control
2022-08-03
phs001203
Stockholm-Tartu Atherosclerosis Reverse Network Engineering Task (STARNET)
Case Set
2023-04-26
phs001205
Region-Specific Neural Stem Cell Lineages Revealed by Single-Cell RNA-Sequences from Human Embryonic Stem Cells
Single Cell Analysis
2016-09-01
phs001206
Blepharospasm in a Multiplex African-American Pedigree
Multiplex Families
2016-09-01
phs001207
NHLBI TOPMed: African American Sarcoidosis Genetics Resource
Affected Sib Pairs
2021-02-02
phs001208
Study on the Genetics of Alcoholism (COGA): Smoke screen and exome sequencing
Family
2019-05-21
phs001209
Accurate Immune Repertoire Sequencing Reveals Malaria Infection Driven Antibody Lineage Diversification in Young Children
Cohort
2016-09-09
phs001210
National Cancer Institute (NCI) Study of Lung Cancer and Smoking Phenotypes in African-American Cases and Controls
Case-Control
2016-09-12
phs001211
NHLBI TOPMed - NHGRI CCDG: Atherosclerosis Risk in Communities (ARIC)
Case-Control
2020-10-08
phs001212
NextGen Consortium: Globin Gene Expression in Sickle Cell Genotype-Specific iPS Cells
Case Set
2016-09-12
phs001213
Molecular Genetics of Heroin Dependence in China
Affected Sib Pairs
2020-02-24
phs001214
DNA and RNA Profiling Using Simultaneous Sequencing (Simul-seq)
Case Set
2016-09-15
phs001215
NHLBI TOPMed: San Antonio Family Heart Study (SAFHS)
Family
2020-10-08
phs001216
A Genome-Wide Association Study for Post-bronchodilator Lung Function in Children with Asthma
Cohort
2016-09-19
phs001217
NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Cohort
2020-10-08
phs001218
NHLBI TOPMed: Genetic Study of Atherosclerosis Risk (GeneSTAR)
Family
2020-10-08
phs001219
Detection of Genes Predisposing to Hematologic Malignancies
Family
2016-09-22
phs001221
ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer
Cohort
2016-09-30
phs001222
Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC)
Case-Control
2016-10-06
phs001223
Analysis of AR Gene Rearrangements in Prostate Cancer
Case Set
2016-10-06
phs001224
Platinum Genomes
Control Set
2016-10-07
phs001226
Regulatory Genomics of Human Embryonic Development
Control Set
2016-10-12
phs001227
Washington University Coronary Artery Disease Study
Case-Control
2016-10-12
phs001228
Gabriella Miller Kids First (GMKF) Pediatric Research Program in Susceptibility to Ewing Sarcoma Based on Germline Risk and Familial History of Cancer
Parent-Offspring Trios
2016-10-17
phs001229
Sequencing Lymphoma
Single Cell Analysis
2016-10-17
phs001230
Estonian Biobank | Estonian Genome Center, University of Tartu
Cohort
2016-10-19
phs001231
The Library of Integrated Network-Based Cellular Signatures (LINCS) - NeuroLINCS
Case-Control
2017-06-01
phs001232
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Cross-Sectional
2022-07-07
phs001233
Disease Severity in Familial Dysautonomia
Case Set
2016-10-21
phs001234
Targeted Sequencing of Primary ER-positive Breast Tumors Treated with 5 Years of Tamoxifen
Case Set
2016-10-25
phs001235
Susceptibility to Respiratory Infections Due to Autosomal Recessive IFIH1 Mutations
Case-Control
2016-10-28
phs001237
NHLBI TOPMed: Women's Health Initiative (WHI)
Longitudinal
2020-10-08
phs001238
Genetic Epidemiology Network of Arteriopathy (GENOA)
Sibling Cohort
2018-06-14
phs001239
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Phase 2)
Case Set
2016-11-07
phs001241
Clonal Architectures and Driver Mutations in Metastatic Melanomas
Case Set
2016-11-08
phs001242
Small Genomic Insertions Form Enhancers that Misregulate Oncogenes
Sequencing
2016-11-10
phs001243
Genetic Basis of Breast Cancer Resistance in BRCA1 Mutation Carrier
Case Set
2016-11-10
phs001244
Nasopharynx Cancer Whole Exome Sequencing
Cohort
2016-11-14
phs001245
Autosomal recessive CD70 deficiency is associated with combined immunodeficiency and EBV viremia
Case-Control
2016-11-14
phs001246
Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome
Case-Control
2016-11-15
phs001247
GMKF: Kids First Pediatric Research Program on Congenital Cranial Dysinnervation Disorders and Related Birth Defects
Cohort
2016-11-15
phs001248
Validation of Gene Array to Predict Bacterial Co-infection In Adults Hospitalized with Viral Lower Respiratory Tract Infections (LRTI)
Case Set
2016-11-15
phs001249
Chemosensitive Relapse in Small Cell Lung Cancer Patient-Derived Xenografts
Case Set
2016-11-16
phs001250
Sequencing of Coding and Non-coding Regions in Primary Breast Cancers and Patient-matched Controls
Cohort
2016-11-17
phs001251
Family-Based Study on Ulcerative Colitis with Whole Exome Sequencing
Family
2016-11-17
phs001252
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Case-Control
2016-11-17
phs001253
Pharmacogenetics of Efavirenz Discontinuation for Reported Central Nervous System Symptoms Appears to Differ by Race
Case-Control
2016-11-22
phs001255
Molecular Evolution of Cancer
Tumor vs. Matched-Normal
2016-12-09
phs001256
Genetic Etiology of Hypoplastic Left Heart Syndrome
Case-Control
2017-05-12
phs001257
Loss of IFN-gamma Signaling in Tumor Cells Associates with Primary Resistance to Anti-CTLA-4 Therapy
Case Set
2017-03-15
phs001258
Total exRNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects
Longitudinal
2019-09-19
phs001259
CCDG CVD: VIRGO - Variation in Recover-Role of Gender on Outcomes of Young Acute Myocardial Infarction (AMI) Patients
Observational
2016-12-16
phs001260
Metagenomic Epidemiology of Antibiotic Resistance in Infectious Diarrhea
Cohort
2016-12-22
phs001261
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Case Set
2016-12-27
phs001263
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis
Case-Control
2016-12-29
phs001264
A super-enhancer associated with CD47 links pro-inflammatory signaling to CD47 upregulation in breast cancer
Xenograft
2017-01-03
phs001265
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - OncoArray Genotypes
Case-Control
2017-01-05
phs001266
Genome-Wide Analysis for Addiction Susceptibility Genes
Affected Sib Pairs
2020-02-27
phs001267
CIDR/NICHD Genetic Basis of Recessive Pediatric Brain Diseases - Group 2
Cohort
2017-01-11
phs001270
Investigating Genetics of Human Natural Short Sleepers (IGHNSS)
Longitudinal
2017-01-19
phs001271
Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK)
Case-Control
2017-01-23
phs001272
Broad Institute Center for Mendelian Genomics
Cohort
2017-01-24
phs001273
Oncoarray Consortium - Lung Cancer Studies
Case-Control
2023-07-07
phs001275
Differential Gene Expression in Cryptorchid Testes
Case-Control
2017-01-26
phs001276
Single-cell Profiling of an In Vitro Model of Human Interneuron Development Reveals Temporal Dynamics of Cell Type Production and Maturation
Single Cell Analysis
2017-01-26
phs001277
NHGRI Genome Integrity of iPSCs Study
Case-Control
2017-01-26
phs001278
Longitudinal Study of the Porphyrias
Longitudinal
2017-01-30
phs001279
Cross-Sectional Characterization of Idiopathic Bronchiectasis
Cross-Sectional
2019-04-01
phs001280
Exome Sequencing of Chordoma Cases
Case Set
2017-01-31
phs001281
Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step toward Biomarker Development
Observational
2019-02-15
phs001282
Pathogenesis and Immunity in Endemic Burkitt Lymphoma
Case Set
2023-02-19
phs001284
National Cancer Institute (NCI) Waldenstrom Macroglobulinemia Genome-wide Association Study
Case-Control
2017-02-02
phs001285
Response and Resistance to ER-Directed Therapy in Metastatic Breast Cancer
Case Set
2017-02-02
phs001286
The Prostate, Lung, Colon, Ovary Screening Trial (PLCO)
Cohort
2022-07-11
phs001287
CPTAC Proteogenomic Study
Case Set
2023-06-06
phs001288
Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis
Longitudinal
2017-02-06
phs001289
Andersen-Tawil Syndrome: Genotype-phenotype correlation and longitudinal study
Longitudinal
2017-02-06
phs001290
CIDR: NCI Genome Wide Predictors of Survival in Colorectal Cancer
Clinical Trial
2017-02-06
phs001291
Neoadjuvant Trastuzumab Response in Breast Cancer
Case Set
2017-02-06
phs001292
Sleep Abnormalities in Rare Genetic Disorders: Angelman Syndrome, Rett Syndrome, and Prader-Willi Syndrome
Case-Control
2019-01-28
phs001293
NHLBI TOPMed: HyperGEN - Genetics of Left Ventricular (LV) Hypertrophy
Family
2021-05-24
phs001295
Development and Validation of a Disability Severity Index for Charcot-Marie-Tooth Disease (CMT)
Cross-Sectional
2019-04-18
phs001296
Investigation of Brain Nitrogen Metabolism in Partial Ornithine Transcarbamylase Deficiency (OTCD) Using 1H MRS, DTI, and fMRI
Observational
2019-04-18
phs001297
Prematurity and Respiratory Outcome Program: Clinical Research Center Study of Functional and Lymphocytic Markers of Respiratory Morbidity in Hyperoxic Preemies
Observational
2017-02-14
phs001298
Fine Mapping of Eight Psoriasis Susceptibility Loci
Case-Control
2017-02-16
phs001299
Nicotine Addiction Genetics and Correlates
Affected Sib Pairs
2020-02-27
phs001300
NABEC: North American Brain Expression Consortium
Control Set
2022-11-01
phs001303
Genome-Wide Association Study of Sporadic and Familial Testicular Germ Cell Tumors
Case-Control
2017-02-21
phs001304
National Cancer Institute (NCI) Biospecimen Pre-analytical Variables (BPV) Analysis
Case Set
2017-02-22
phs001305
A Randomized, Double-Blind, Crossover Study of Sodium Phenylbutyrate (Buphenyl) and Low-Dose Arginine (100 mg/kg/day) Compared to High-Dose Arginine (500 mg/kg/day) Alone on Liver Function, Ureagenesis and Subsequent Nitric Oxide Production in Patients with Argininosuccinic Aciduria (ASA)
Interventional
2017-02-24
phs001306
Large Scale Meta-analysis Characterizes Genetic Architecture for Common Psoriasis-associated Variants
Case-Control
2017-02-27
phs001307
Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Case-Control
2017-02-27
phs001309
Multicenter International Cross-Sectional Evaluation of Pulmonary Alveolar Proteinosis (MICEPAP) Trial
Clinical Trial
2017-02-27
phs001310
Early Onset and Progression of Primary Ciliary Dyskinesia Lung Disease Prior to 10 Years of Age
Observational
2019-04-18
phs001311
Phase II Therapeutic Trial of Mexiletine in Non-Dystrophic Myotonia (IND #77,021)
Case Set
2017-02-27
phs001312
National Eye Institute (NEI) Primary Open-Angle African American Glaucoma Genetics (POAAGG) Study
Case-Control
2017-02-27
phs001313
Modifier Genes in 21-hydroxylase Deficiency
Clinical Trial
2017-02-27
phs001314
Potential Modulatory Role of Osteoprotegerin in Bone Metabolism of Patients with 21-Hydroxylase Deficiency
Case-Control
2017-02-27
phs001315
GECCO: Detecting Common and Rare Genetic Loci and GxE Interactions in Colorectal Cancer
Case-Control
2017-02-27
phs001316
Therapeutic Trial of Potassium and Acetazolamide in Andersen-Tawil Syndrome
Clinical Trial
2017-02-27
phs001317
Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Clinical Trial
2017-02-28
phs001318
A Phase I/II Study of Revlimid (lenalidomide) in Combination with Vidaza (azacitidine) in Patients with Advanced Myelodysplastic Syndrome (MDS)
Case Set
2017-03-01
phs001319
Glioma International Case Control Study (GICC)
Case-Control
2017-03-01
phs001320
Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi
Prospective
2017-03-02
phs001321
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) - OncoArray Genotypes
Cohort
2017-03-02
phs001322
NINDS Inherited Forms of Motor Neuron Disease Study
Cohort
2022-02-01
phs001323
Multiple Myeloma Genomic Study (MMGS)
Cohort
2021-10-13
phs001325
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for Studying the Impact of Genetic Variation on Molecular and Physiological Phenotypes - Whole Genome Sequence
Family
2019-11-22
phs001326
A Retrospective and Cross-Sectional Analysis of Patients Treated for SCID Since January 1, 1968
Longitudinal
2019-04-22
phs001327
Childhood Cancer Survivor Study (CCSS)
Cohort
2020-12-03
phs001328
Longitudinal Studies of Brain Structure and Function in MPS Disorders
Longitudinal
2017-03-08
phs001329
The Natural History of Mucolipidosis Type IV
Longitudinal
2019-01-02
phs001330
Characterizing the Neurobehavioral Phenotype(s) in MPS III (Pilot Study)
Longitudinal
2019-11-07
phs001331
Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT)
Longitudinal
2019-08-30
phs001332
Natural History of and Genetic Modifiers in Spinocerebellar Ataxias
Observational
2019-11-07
phs001333
Natural History and Structural Functional Relationships in Fabry Renal Disease
Longitudinal
2019-08-29
phs001336
Extracorporeal Life Support Survival in a Pediatric Hematopoietic Cellular Transplant Recipient with Presumed Graft Versus Host Disease-Related Fulminant Myocarditis
Case Set
2017-03-22
phs001337
AACR Project Genomics, Evidence, Neoplasia, Information, Exchange (GENIE)
Case Set
2017-03-22
phs001338
A whole-genome sequencing study for evolutionary history of Tibetans and their genetic adaptations to high altitude
Population
2017-03-24
phs001339
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Case Set
2017-03-24
phs001340
Identification and Targeting of Inflammatory Macrophage-Fibroblast Crosstalk in Rheumatoid Arthritis
Case Set
2017-03-27
phs001341
The National Heart, Lung, and Blood Institute (NHLBI)-funded Next Generation Genetic Association Studies (NextGen) Consortium: Phenotyping Lipid traits in iPS derived hepatocytes Study (PhLiPS Study)
Cohort
2017-03-28
phs001342
Exome Sequencing of Statin-Induced Myopathy Cases
Case-Control
2017-03-30
phs001343
Whole Exome Sequences of Human Embryonic Stem Cell Lines
Control Set
2017-03-31
phs001344
GnRH Agonist-Induced Ovarian Suppression and Ovarian Steroids in PMDD and Controls
Case-Control
2017-03-31
phs001345
NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)
Cohort
2020-10-08
phs001346
Human Gene Expression Patterns Associated with Experimental P. falciparum Infection
Clinical Trial
2017-03-31
phs001347
Impact of Respiratory Virus Infections and Bacterial Microbiome Shifts on Lymphocyte and Respiratory Function in Infants Born Prematurely or Full Term
Observational
2019-02-26
phs001348
Biesecker Lab (NHGRI) Whole Genome Medical Sequencing for Gene Discovery
Parent-Offspring Trios
2017-09-15
phs001349
Identification of 22 Novel Loci Associated with Susceptibility to Testicular Germ Cell Tumors
Case-Control
2019-10-07
phs001350
Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)
Cohort
2017-04-06
phs001351
Research Study into The Molecular Genetics of Hereditary Neuropathies
Case Set
2017-04-06
phs001352
Metagenomics-Guided Pathogen Discovery in Travelers' Diarrhea
Cohort
2017-04-06
phs001357
The Genomic Landscape of Tuberous Sclerosis Complex (TSC)
Case-Control
2017-04-13
phs001358
RareBliss: Rare Bipolar Loci Identification Through Sequencing Study
Case-Control
2017-04-17
phs001359
NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate
Longitudinal
2021-05-24
phs001360
The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Consortium for the Longitudinal Evaluation of African-Americans with Early Rheumatoid Arthritis (CLEAR)
Case-Control
2017-04-18
phs001361
National Eye Institute (NEI) Genetic Epidemiology of Age-Related Macular Degeneration in the Old Order Amish
Family
2018-12-12
phs001362
Linked Read Sequencing of Gastric Cancer Metastases for Complex SV Resolution
Case-Control
2017-04-25
phs001363
The Pioneer 100 Wellness Project (P100)
Longitudinal
2017-04-25
phs001364
Mapping the Human Connectome - Structure, Function, and Heritability: Healthy Young Adults (Age 22-35 Years) Including Twins and their Non-Twin Siblings
Control Set
2017-04-27
phs001365
Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab on NSABP B-40
Case-Control
2017-04-28
phs001366
A prospective pilot study of genome-wide exome and transcriptome profiling in patients with small cell lung cancer progressing after first-line therapy
Case Set
2017-04-28
phs001367
Add Health: Longitudinal Study of a Nationally Representative Sample of Adolescents in Grades 7-12 in the United States during the 1994-95 School Year, Followed into Adulthood with Five Interviews/Surveys in 1995, 1996, 2001-02, 2008, and 2016-18.
Longitudinal
2017-04-28
phs001368
NHLBI TOPMed: Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Project: Cardiovascular Health Study
Longitudinal
2020-10-08
phs001369
Germline hypomorphic CARD11 mutations in severe atopic disease
Case-Control
2017-05-09
phs001370
Whole Exome Sequencing of Uveal Melanoma
Cohort
2017-05-15
phs001371
TNF-induced dynamic regulation of mRNA stabilome in rheumatoid arthritis fibroblast-like synoviocytes
Case Set
2017-05-16
phs001372
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Case Set
2017-05-19
phs001373
Brain cell type-specific enhancer-promoter connectivity maps and disease risk association
Case Set
2019-07-26
phs001374
VA APOLLO Project - Research for Precision Oncology (RePOP)
Longitudinal Cohort
2019-09-13
phs001375
Slim Initiative in Genomic Medicine for the Americas (SIGMA): Mexico City Diabetes Study (MCDS)
Case-Control
2021-03-02
phs001376
Autosomal Recessive CD55 Deficiency is Associated with Protein Losing Enteropathy, Thrombosis, and Complement Dysregulation
Case-Control
2017-06-05
phs001377
Epigenetics of Cocaine and Nicotine Addiction
Case Set
2017-06-08
phs001378
Single-cell RNA-Seq of human lymphoma reveals malignant B cell diversity and patterns of T cell immune checkpoint co-expression
Case-Control
2017-06-09
phs001379
A Joint Linkage/Association Strategy to Interrogate AMD Genetic Susceptibility
Case-Control
2017-06-12
phs001380
Genomic Studies of Gilles de la Tourette Syndrome
Case-Control
2017-06-13
phs001381
Gut Microbiome and Types of Colorectal Polyps
Cross-Sectional
2017-06-16
phs001382
Reproductive Health in Men and Women with Vasculitis
Clinical Trial
2017-06-16
phs001383
Birth Defects: Moebius Syndrome and Related Congenital Facial Weakness Disorders
Case Set
2017-06-16
phs001384
Time Lapse to Cancer-Defining the Transition from Polyp to Cancer
Case Set
2017-06-19
phs001385
Evaluation of Ancestry Admixture among Chileans
Case-Control
2017-06-19
phs001386
Smoking and the Vaginal Microbiome
Case-Control
2018-01-05
phs001387
NHLBI TOPMed: Rare Variants for Hypertension in Taiwan Chinese (THRV)
Cohort
2021-05-25
phs001388
Slim Initiative in Genomic Medicine for the Americas (SIGMA): Diabetes in Mexico Study (DMS)
Case-Control
2021-03-02
phs001389
University of Texas at Austin (UTA) Histone Modification and Gene Expression Profiling in 9 Primary Glioblastoma Multiforme, 2 Anaplastic Astrocytomas and Two Meningiomas
Case Set
2017-06-22
phs001391
OncoArray: Prostate Cancer
Case-Control
2017-06-23
phs001392
A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children with SCID Disorders
Longitudinal
2019-04-17
phs001394
The Hypertension-Insulin Resistance Family Study (HTN-IR)
Cohort
2017-06-27
phs001395
NHLBI TOPMed - NHGRI CCDG: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
Cohort
2020-10-08
phs001396
Genetics of Pigmentation in Eastern and Southern African Populations Study
Cohort
2017-06-29
phs001397
The Mexican-American Coronary Artery Disease Study (MACAD)
Cohort
2017-06-30
phs001398
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Bangladesh Risk of Acute Vascular Events (BRAVE) Study
Cohort
2017-06-30
phs001399
Development of Precision Neoadjuvant-Adjuvant Therapies
Case Set
2017-06-30
phs001400
Advanced Genomic Techniques in Sequencing of Colorectal Cancer
Case-Control
2017-07-05
phs001402
NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE)
Case Set
2021-06-03
phs001403
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Case-Control
2017-07-07
phs001404
Molecular Profiling of Gallbladder Cancer (MPOG)
Case Set
2017-07-07
phs001405
LCCC1122: Defining the Triple Negative Breast Cancer Kinome Response to GSK1120212
Clinical Trial
2017-07-07
phs001406
National Institute of Mental Health (NIMH) Duke Cognition Cohort
Control Set
2017-07-07
phs001407
HNPCC-Sys: Molecular Characterization of Lynch Syndromes
Tumor vs. Matched-Normal
2017-07-10
phs001409
Understanding the genetic risk underlying racial disparities in uterine fibroids
Case-Control
2017-07-10
phs001410
Kids First: Pediatric Research Project on Adolescent Idiopathic Scoliosis
Cohort
2020-12-17
phs001411
Action to Control Cardiovascular Risk in Diabetes (ACCORD) Clinical Trial
Cohort
2017-07-14
phs001412
NHLBI TOPMed: Diabetes Heart Study (DHS) African American Coronary Artery Calcification (AA CAC)
Cohort
2020-10-08
phs001413
Large Scale Genotyping of Psychiatric Disorders
Case-Control
2017-07-18
phs001415
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Case-Control
2017-07-21
phs001416
NHLBI TOPMed: MESA and MESA Family AA-CAC
Family
2020-08-18
phs001417
Scalable Whole-Exome Sequencing of Cell-Free DNA Reveals High Concordance with Metastatic Tumors
Case Set
2021-03-23
phs001418
Interpreting molecular role of DNA variants associated with Crohn's Disease through integrative analysis of open chromatin, epigenome and transcriptome data in diverse and relevant tissues and cells
Case-Control
2017-07-31
phs001419
A Natural History Study of CMT1B, CMT2A, CMT4A and CMT4C
Longitudinal
2017-07-31
phs001420
Kids First: Genomics of Orofacial Cleft Birth Defects in Latin American Families
Parent-Offspring Trios
2017-08-02
phs001421
Whole exome sequencing and methylation profiling of uveal melanoma
Cohort
2017-08-03
phs001422
GEnomics and Transcriptomics of Human INsulinoma (GETHIN)
Case-Control
2020-12-04
phs001423
Tourette International Collaborative Genetics (TIC Genetics) Study - NJCTS and NIMH
Multiplex Families
2021-01-25
phs001424
Genomic Analysis of Pre-Treatment and Autopsy Glioblastoma Specimens
Longitudinal
2017-08-04
phs001425
Integrative Analysis of Tumor Biopsies on Sequential CTLA-4 and PD-1 Blockade Reveals Markers of Response and Resistance
Case Set
2017-08-08
phs001426
Type 1 Diabetes Genetics Consortium (T1DGC): Case-only RNA-Seq Study
Case Set
2017-08-11
phs001427
Resistance to Checkpoint Blockade Therapy Through Inactivation of Antigen Presentation
Longitudinal
2021-01-13
phs001428
Genome-Wide Predictors of Treatment-Related Toxicities in SWOG S0221 Trial
Clinical Trial
2017-08-14
phs001430
Smith-Lemli-Opitz Syndrome: A Longitudinal Clinical Study of Patients Receiving Cholesterol Supplementation
Longitudinal
2020-01-28
phs001431
Whole Exome and Whole Genome Profiling as well Genome-Wide Methylation Profiling from Early to Advanced Chronic Lymphocytic leukemia (CLL), Genome-Wide Methylation Profiling in Monoclonal B Cell Lymphocytosis (MBL)
Case Set
2022-02-09
phs001432
A Pilot Study of Rapid Autopsy and Procurement of Tissue in Thoracic Malignancy Cancer Patients to Investigate Tumor Heterogeneity
Case Set
2017-08-17
phs001433
Non-coding RNAs Activated by the Wnt/Beta-catenin Signaling Pathway in Hepatoblastoma
Case-Control
2017-08-18
phs001434
NHLBI TOPMed: Defining the Time-Dependent Genetic and Transcriptomic Responses to Cardiac Injury Among Patients with Arrhythmias
Case Set
2021-06-08
phs001435
NHLBI TOPMed: Australian Familial Atrial Fibrillation Study
Case Set
2021-06-08
phs001436
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Parent-Offspring Trios
2017-08-21
phs001437
Pediatric Preclinical Testing Consortium (PPTC)
Cohort
2017-08-21
phs001438
The Dynamic Landscape of Open Chromatin During Human Cortical Neurogenesis
Collection
2017-08-21
phs001439
University of Utah Pelvic Organ Prolapse Disorder Study
Case Set
2017-08-21
phs001441
Admixture Mapping of Staphylococcus aureus Bacteremia
Case-Control
2017-08-22
phs001442
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Longitudinal
2022-04-08
phs001444
Genomic Variation in Diffuse Large B Cell Lymphomas
Case Set
2019-11-04
phs001446
NHLBI TOPMed: Severe Asthma Research Program (SARP)
Case Set
2021-06-14
phs001447
Genomic Resistance Patterns to Second Generation Androgen Blockade in Paired Tumor Biopsies of Metastatic Castrate-Resistant Prostate Cancer
Cohort
2017-08-30
phs001448
Subtyping Sub-Saharan Esophageal Squamous Cell Carcinoma by Comprehensive Molecular Analysis
Cohort
2017-09-01
phs001451
A Phase I Study with a Personalized Neoantigen Cancer Vaccine in Melanoma
Clinical Trial
2022-07-05
phs001454
Genomic Regions Associated with Susceptibility to Barrett's Esophagus and Esophageal Adenocarcinoma in African Americans: The Cross BETRNet Admixture Study
Case Set
2017-09-11
phs001455
Screening Cases of Isolated Dystonia for Variants in CIZ1
Case Set
2017-09-12
phs001457
Accelerating Medicines Partnership-Rheumatoid Arthritis (AMP-RA/SLE)
Case-Control
2017-09-15
phs001458
Deep Sequencing Studies for Cannabis and Stimulant Dependence
Family
2017-09-15
phs001459
Accelerating Medicines Partnership-Systemic Lupus Erythematosus (AMP-RA/SLE)
Case-Control
2017-09-15
phs001460
Genomic-Enabled Medicine for Recurrent Glioblastoma
Case Set
2020-04-23
phs001461
Temporal and Clonal Progression in Pediatric Ependymoma
Longitudinal
2017-09-19
phs001463
Differential Transcription Start Site Usage in Brain-related Samples
Control Set
2017-09-20
phs001464
Impaired HLA Class I Antigen Processing and Presentation as a Mechanism of Acquired Resistance to Immune Checkpoint Inhibitors in Lung Cancer
Cohort
2017-09-25
phs001465
Multiregion Sequencing of Localized Prostate Cancer
Case Set
2017-09-26
phs001466
NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)
Case Set
2021-06-15
phs001467
NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)
Case-Control
2021-07-09
phs001468
NHLBI TOPMed: Recipient Epidemiology and Donor Evaluation Study-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Cohort
2021-09-02
phs001469
High response rate to anti PD-1 therapy in desmoplastic melanoma
Cohort
2017-10-10
phs001470
Study of Women's Health Across the Nation (SWAN) Repository
Longitudinal
2017-10-16
phs001471
National Heart, Lung, and Blood Institute (NHLBI) Heart Healthy Lenoir (HHL) Genomics Study
Interventional
2017-10-16
phs001472
NHLBI TOPMed: Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Case-Control
2021-07-06
phs001473
Clonal Evolution and Transcriptomic Analysis of Chronic Lymphocytic Leukemia Treated with Ibrutinib
Longitudinal
2021-11-09
phs001474
Single cell RNA-seq reveals malignant and stromal programs associated with metastasis in head and neck cancer
Cohort
2017-10-24
phs001475
Field Studies of Human Immunity to Amebiasis in Bangladesh (NIH Birth Cohort) and Exploration of the Biologic Basis for Underperformance of Oral Polio and Rotavirus Vaccines in Bangladesh (PROVIDE)
Longitudinal Cohort
2017-10-25
phs001479
A Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B is Associated with Leukocytosis, Lymphadenopathy, Splenomegaly, Necrotizing Granulomas, Hyper-IgM and Thrombocytopenia
Case-Control
2017-10-27
phs001480
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Case-Control
2017-11-02
phs001481
Etiological Investigation of Cancer Susceptibility in Inherited Bone Marrow Failure Syndromes: A Natural History Study
Prospective
2017-11-03
phs001482
Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening
Cohort
2017-11-06
phs001483
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - germline whole genome sequencing
Case Set
2017-11-08
phs001484
Pharmacogenomics of HIV Therapy - Atazanavir Bilirubin-related Side Effects
Case-Control
2017-11-08
phs001485
Somatic Mutations and Cell Lineage in the Human Brain
Case Set
2022-04-28
phs001486
NCI Cancer Model Development for the Human Cancer Model Initiative (HCMI)
Longitudinal Cohort
2019-10-09
phs001487
Center Common Disease Genomics [CCDG] - CVD - TAICHI
Observational
2017-11-16
phs001488
Creatine in Huntington's Disease (HD) (CREST-E)
Multicenter
2017-11-17
phs001489
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium
Case-Control
2019-08-15
phs001490
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: BioMe Biobank Program
Case-Control
2017-11-29
phs001491
Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption
Case-Control
2023-04-11
phs001492
Genome-Wide Association Study on Calcific Aortic Valve Stenosis in Quebec (QUEBEC-CAVS)
Case-Control
2017-11-30
phs001493
Genomic Predictors of Response to Immune Checkpoint Therapy
Cohort
2018-08-07
phs001494
AIDS Linked to the Intravenous Experience (ALIVE) Cohort
Longitudinal
2017-12-01
phs001495
DAXX restoration suppresses alternative lengthening of telomeres in ATRX wild-type cells
Case Set
2019-01-30
phs001496
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Case-Control
2017-12-05
phs001497
UCSF Adult Glioma Study
Case-Control
2021-08-20
phs001498
INSIGHT (Intervention Nurses Start Infants Growing on Healthy Trajectories) Cohort
Cohort
2019-04-16
phs001499
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis
Case-Control
2017-12-05
phs001500
National Cancer Institute (NCI) Primary Human Melanocyte QTL Study
eQTL
2021-04-23
phs001501
Impact of Race and Genetic Factors on Beta Blocker Effectiveness in Heart Failure
Longitudinal Cohort
2017-12-07
phs001502
Center for Common Disease Genomics (CCDG)-Cardiovascular: University of Pennsylvania Cohort
Case-Control
2017-12-11
phs001503
Women's Interagency HIV Study (WIHS)
Prospective
2017-12-12
phs001504
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: Research Studies in Hong Kong
Case-Control
2021-03-02
phs001505
Host Genetic Determinants of the Outcome of Staphylococcus Aureus Bacteremia by Whole Exome Sequencing
Case-Control
2017-12-12
phs001507
Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor
Multiplex Families
2017-12-15
phs001508
Genetic Analysis of Metopic Nonsyndromic Craniosynostosis
Case Set
2017-12-15
phs001511
Progress in Diabetes Genetics in Youth (ProDIGY) Exome Sequencing Study: SEARCH for Diabetes in Youth
Case-Control
2017-12-15
phs001512
Gene Expression Signatures Characterized by Longitudinal Stability and Inter-Individual Variability Delineate Baseline Phenotypic Groups with Distinct Responses to Immune Stimulation
Methods Development
2017-12-18
phs001513
Mechanisms of Chemotherapy Resistance in T-ALL
Cohort
2017-12-18
phs001514
NHLBI TOPMed: Walk-PHaSST Sickle Cell Disease (SCD)
Clinical Trial
2021-06-16
phs001515
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Cross-Sectional
2021-05-11
phs001516
Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns
Cohort
2018-01-03
phs001517
Genetics of Human Inherited Retinal Diseases (GHIRD)
Case Set
2022-05-18
phs001518
Translational Research Investigating Underlying disparities in acute Myocardial infarction Patients' Health status (TRIUMPH)
Longitudinal Cohort
2018-01-09
phs001519
A Phase I Study With a Personalized Neoantigen Cancer Vaccine in Glioblastoma Multiforme
Case Set
2018-01-10
phs001521
Immunoprotective mechanisms and microbiota interplay in Salmonella Typhi infection
Longitudinal
2018-01-16
phs001522
Germline
Parent-Offspring Trios
2018-01-16
phs001523
Multi-Omic Microbiome Study-Pregnancy Initiative (MOMS-PI)
Longitudinal
2018-01-17
phs001524
The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation
Case Set
2020-03-03
phs001525
Genome and Transcriptome Assembly Reveals SVA-Mediated Aberrant Splicing in X-Linked Dystonia Parkinsonism
Cohort
2021-05-02
phs001526
Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies
Sequencing
2018-01-23
phs001527
Oral Microbiome in Esophageal Adenocarcinoma
Case-Control
2018-01-23
phs001528
Gene Expression of Small Cell Carcinoma of the Ovary-Hypercalcemic Type (SCCOHT)
Case Set
2022-10-19
phs001529
Single-cell RNA-seq of rheumatoid arthritis synovial tissue using low-cost microfluidic instrumentation
Case Set
2018-01-26
phs001531
Whole exome sequencing to discover genetic variation associated with aortopathy in Turner Syndrome
Case-Control
2018-01-31
phs001532
Nicotine dependence GWAS meta-analysis across European and African American ancestries
Case-Control
2020-04-16
phs001534
Pathways Study
Longitudinal
2018-02-05
phs001535
Offspring Sex Impacts DNA Methylation and Gene Expression in Placentae from Women with Diabetes during Pregnancy
Nested Case-Control
2018-02-05
phs001538
North American Mitochondrial Disease Consortium Patient Registry and Biorepository
Methods Development
2018-02-06
phs001539
Myocardial Applied Genomics Network (MAGNet) Study
Case-Control
2022-07-07
phs001541
Anorexia Nervosa Genetics Initiative (ANGI)
Case-Control
2018-02-13
phs001542
NHLBI TOPMed: Genetics of Asthma in Latino Americans (GALA)
Case Set
2021-09-17
phs001543
NHLBI TOPMed - NHGRI CCDG: AF Biobank LMU in the context of the MED Biobank LMU
Case Set
2021-06-17
phs001544
NHLBI TOPMed - NHGRI CCDG: Malmo Preventive Project (MPP)
Case Set
2021-06-17
phs001545
NHLBI TOPMed - NHGRI CCDG: Intermountain INSPIRE Registry
Case Set
2021-06-24
phs001546
NHLBI TOPMed: Determining the Association of Chromosomal Variants with Non-PV Triggers and Ablation-Outcome in AF (DECAF)
Longitudinal
2021-06-24
phs001547
NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study
Case Set
2021-06-24
phs001548
TCR Repertoire Sequencing to Evaluate the Diversity of Follicular Helper T Cells in HIV Infected Lymph Nodes
Cohort
2021-12-15
phs001549
Genome-wide Association Study and Meta-Analysis of Ewing Sarcoma
Case-Control
2018-02-15
phs001550
The Genetic and Transcriptomic Evolution of Melanoma
Tumor
2022-06-14
phs001551
Epilepsy Genetics Initiative
Parent-Offspring
2018-02-16
phs001552
Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow up Study: Pakistan Genomic Resource (PGR)
Case-Control
2018-02-23
phs001553
Development of CMT Peds Scale for Children with CMT
Longitudinal
2018-03-05
phs001554
Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide Sequencing
Case-Control
2022-09-09
phs001555
Determination of Cross-Reactive Immunological Material (CRIM) status and longitudinal follow-up of individuals with Pompe disease
Longitudinal
2018-03-06
phs001556
BRAIN Cell EncyclOpeDia of Transcribed Elements (BRAINcode)
Control Set
2018-03-06
phs001557
Mosaic Chromosomal Aneuploidies Detection in Clinical Samples
Case-Control
2018-03-08
phs001559
Contribution of Genetic Polymorphisms to the Abuse Liability of Oxycodone
Case Set
2018-03-13
phs001560
Novel Factors for Unexplained Phenotypes of Subclinical Carotid Atherosclerosis
Case-Control
2018-03-13
phs001561
WES Elucidation of Pathogenetic Mechanisms for Immune System Disorders and NIAID Pilot of Genetic Incidental Finding Management
Case Set
2018-03-13
phs001563
Blood Handling and Leukocyte Isolation Methods Impact the Global Transcriptome of Immune Cells
Control Set
2018-03-20
phs001564
Structure and diversity of urinary cell-free DNA informative of host-pathogen interactions in human urinary tract infection
Case-Control
2020-01-27
phs001565
Genomic Correlates of Response and Resistance to Immune Checkpoint Blockade in Solid Tumors
Case Set
2018-03-26
phs001566
Metaplastic breast cancer in a patient with neurofibromatosis type 1 and somatic loss of heterozygosity
Case Set
2018-03-26
phs001568
Genetic Epidemiology of Chronic Lymphocytic Leukemia
Case-Control
2018-04-02
phs001570
CALGB 40601: Randomized Phase III Trial of Paclitaxel Combined With Trastuzumab, Lapatinib, or Both As Neoadjuvant Treatment of HER2-Positive Primary Breast Cancer
Case Set
2022-06-02
phs001571
Genetic Study of Inflammatory Bowel Disease (IBD) in African Americans
Case-Control
2018-04-09
phs001572
Pan-tumor genomic biomarkers for personalization of PD-1 checkpoint blockade based immunotherapy
Case Set
2018-04-10
phs001573
Intra-tumor heterogeneity and clonal evolution of papillary renal cell carcinoma
Case Set
2018-04-10
phs001575
Assessment of Neurological Deterioration in Subjects with Late Infantile Neuronal Ceroid Lipofuscinosis
Longitudinal
2019-11-07
phs001576
Longitudinal Study of Bone and Endocrine Disease in Children with MPS I, II, and VI: A Multicenter Study of the Lysosomal Disease Network
Longitudinal
2019-08-29
phs001577
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing
Cohort
2018-04-11
phs001578
The preterm infant microbiome: biological, behavioral and health outcomes at 2 and 4 years of age
Longitudinal Cohort
2018-04-12
phs001580
Massachusetts General Hospital (MGH)/Broad Hurthle cell carcinoma whole exome sequencing study
Cohort
2018-04-20
phs001581
Genomic Characterization of Head and Neck Squamous Cell Carcinoma Cell Lines
Case Set
2018-04-24
phs001584
eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants
Case-Control
2019-12-05
phs001585
Identification of ALS Associated Genes Using Whole Genome Sequencing
Case-Control
2022-06-24
phs001586
Rhode Island Child Health Study (RICHS)
Cohort
2018-04-27
phs001587
Characterization of prostate cancer organoids
Case Set
2018-04-30
phs001588
Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records
Observational
2018-04-30
phs001589
Breast Cancer Family Registry Early-onset Breast Cancer GWAS
Case-Control
2018-05-01
phs001590
National Epidemiologic Survey on Alcohol and Related Conditions-III (NESARC-III)
Genotype
2021-02-03
phs001591
Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease
Cohort
2018-05-01
phs001592
Center for Common Disease Genomics [CCDG] - Cardiovascular ATVB: Atherosclerosis Thrombosis and Vascular Biology
Case-Control
2018-05-03
phs001593
Genome Sequencing of Familial Cholangiocarcinoma for the Identification of Germline Risk Alleles
Parent-Offspring Trios
2018-05-08
phs001594
Mucosal Melanoma Targeted Exome Sequencing Study (UCSF)
Case Set
2018-05-09
phs001595
Norepinephrine Transporter Blockade as a Pathophysiological Biomarker in Neurogenic Orthostatic Hypotension
Longitudinal
2018-05-10
phs001596
Acral melanoma targeted exome sequencing study (UCSF)
Case Set
2018-05-15
phs001597
Genomic Analysis of Bevacizumab-induced Hypertension
Case-Control
2018-05-17
phs001598
NHLBI TOPMed - NHGRI CCDG: The Johns Hopkins University School of Medicine Atrial Fibrillation Genetics Study
Case Set
2021-06-25
phs001599
NHLBI TOPMed: Boston-Brazil Sickle Cell Disease (SCD) Cohort
Cohort
2018-05-17
phs001600
NHLBI TOPMed - NHGRI CCDG: Early-onset Atrial Fibrillation in the CATHeterization GENetics (CATHGEN) Cohort
Case Set
2021-06-30
phs001601
NHLBI TOPMed - NHGRI CCDG: Penn Medicine BioBank Early Onset Atrial Fibrillation Study
Case Set
2021-06-29
phs001602
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP)
Case-Control
2021-06-30
phs001603
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genomics and Environmental Research of Asthma (IGERA)
Case-Control
2021-06-30
phs001604
NHLBI TOPMed: Children's Health Study (CHS) Effects of Air Pollution on the Development of Obesity in Children (Meta-AIR)
Case-Control
2021-06-30
phs001605
NHLBI TOPMed: Chicago Initiative to Raise Asthma Health Equity (CHIRAH)
Case Set
2021-07-02
phs001606
NHLBI TOPMed: Early-Onset Atrial Fibrillation in the Estonian Biobank
Case Set
2021-07-02
phs001607
NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing
Case Set
2021-07-26
phs001608
NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG)
Case Set
2020-10-08
phs001609
Genetic contributions of lupus nephritis in a multi-ethnic cohort of systemic lupus erythematosus (SLE)
Case-Control
2018-05-21
phs001611
Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer
Cohort
2018-05-30
phs001612
NHLBI TOPMed: Coronary Artery Risk Development in Young Adults (CARDIA)
Longitudinal
2018-05-30
phs001615
Comprehensive Epigenetic Landscape of Rheumatoid Arthritis Fibroblast-Like Synoviocytes
Case-Control
2018-06-04
phs001616
eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel
Cohort
2019-12-10
phs001617
Genetic Causes of Growth Disorders
Family
2018-06-05
phs001618
A Dormant TIL Phenotype Defines Non-Small Cell Lung Carcinomas Sensitive to Immune Checkpoint Blockers
Cohort
2018-06-06
phs001619
Genetic analysis of patients with Inherited Retinal Dystrophies (IRDs) using next generation sequencing to identify the causative variants
Case-Control
2020-06-03
phs001620
Genetic Testing to Understand and Address Renal Disease Disparities
Longitudinal
2018-06-11
phs001621
Genetic Susceptibility and Biomarkers of Platinum-Related Toxicities
Longitudinal
2018-06-11
phs001623
Genomic Analysis of Head and Neck Cancers
Case Set
2019-10-24
phs001624
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study
Case-Control
2021-07-21
phs001625
Whole Genome Sequencing in Psychotic Major Depression
Control Set
2018-06-13
phs001626
Longitudinal Multi'omics of the Human Microbiome in Inflammatory Bowel Disease (IBDMDB)
Case-Control
2018-06-14
phs001627
High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidics
Longitudinal
2018-06-14
phs001628
Clinical Resistance to Crenolanib in Acute Myeloid Leukemia Due to Diverse Molecular Mechanisms
Longitudinal
2018-06-14
phs001629
Single Patient BRAF Mutant Brain Tumor, Pre- and Post-dabrafenib WES.
Case Set
2018-06-15
phs001630
The Immunogenetics of Measles Immunity - Measles (MMR) vaccination (NIAID/NIH)
Cohort
2018-06-16
phs001631
Genetics of Mood Disorders: Aging and Emotion Regulation Brain Circuitry in Bipolar
Case-Control
2018-06-18
phs001632
African American Multiple Myeloma GWAS
Case Set
2018-06-20
phs001641
Implementation, Adoption, and Utility of Family History in Diverse Care Settings
Clinical Trial
2018-06-25
phs001642
Center for Common Disease Genomics [CCDG] - Autoimmune: Inflammatory Bowel Disease (IBD) Exomes and Genomes
Case-Control
2021-05-11
phs001643
Genomic and transcriptomic characterization of chordoma
Case Set
2018-06-26
phs001644
NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai
Cohort
2020-10-08
phs001645
Genomic Landscape of Cutaneous Diffuse Large B Cell Lymphoma
Case Set
2018-06-26
phs001646
Regulatory Changes in Glioblastoma Brain Tumors and Xenografts Wave 1
Case Set
2018-06-29
phs001647
Varieties of Impulsivity in Opiate and Stimulant Users
Case-Control
2021-05-25
phs001648
Genomic Characterization of Metastatic Castration Resistant Prostate Cancer
Cohort
2019-09-23
phs001649
Center for Education and Drug Abuse Research (CEDAR)
Longitudinal
2018-07-06
phs001650
Genetic and Genomic Stability Across Lymphoblastoid Cell Line Expansions
Control Set
2018-07-06
phs001651
Whole Exome Characterization of Squamous Cell Lung Cancers (Lung SQCC) from Appalachian Kentucky (APPKY)
Case Set
2018-07-12
phs001653
Systematic Analysis of Coding and Non-coding Elements in Developmental Pathways Implicated in Holoprosencephaly Pathogenesis
Parent-Offspring Trios
2018-07-20
phs001654
Aspirin and Inflammation: Mutations, Genes, Pathways and Prevention in Barrett's Esophagus
Case-Control
2018-07-20
phs001655
Study of the Human Skin Metagenome Associated with Acne
Case-Control
2018-07-23
phs001657
Functional Genomic Landscape of Acute Myeloid Leukemia
Longitudinal
2020-08-20
phs001658
Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors
Cohort
2018-07-31
phs001659
Bayesian-Based Noninvasive Prenatal Diagnosis of Single-Gene Disorders
Parent-Offspring Trios
2018-08-01
phs001660
Prospective Analysis of Genotypes in Adults Undergoing Therapy for Lung Cancer (Paclitaxel Cohort)
Case Set
2018-08-02
phs001661
NHLBI TOPMed: Genetic Causes of Complex Pediatric Disorders - Asthma (GCPD-A)
Case-Control
2021-07-29
phs001662
NHLBI TOPMed: Lung Tissue Research Consortium (LTRC)
Case-Control
2020-10-08
phs001663
Neoantigen Landscape in a Hypermutated Glioblastoma Arising in a Patient with Germline POLE Deficiency Treated with Checkpoint Blockade Immunotherapy
Longitudinal
2018-08-08
phs001664
Parkinson's Disease Cognitive Genetics Consortium (PDCGC) Stage I, NeuroX Dataset
Case Set
2018-08-10
phs001666
A phase II trial of the aurora kinase A inhibitor alisertib for patients with castration resistant and neuroendocrine prostate cancer: efficacy and biomarker evaluation
Case Set
2018-08-13
phs001667
Genomics of Kidney Transplantation
Cohort
2018-08-13
phs001672
Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies
Cohort
2022-12-09
phs001673
ADAGESIII: Contribution of genotype to glaucoma phenotype in African Americans
Case-Control
2018-08-16
phs001674
The Genomic Landscape of Endocrine Resistant Advanced Breast Cancers: Paired Pre- and Post-endocrine Therapy Samples.
Case Set
2018-08-23
phs001675
Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families
Nuclear Families
2018-08-27
phs001676
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Autism - Simons Simplex Collection (SSC)
Family
2018-08-27
phs001677
Adolescent Idiopathic Scoliosis (AIS) 1000 Exomes Study
Case Set
2018-08-28
phs001678
High-throughput determination of the antigen specificities of T cell receptors in single cells
Single Cell Analysis
2018-08-30
phs001679
TRanscriptomic ANalySis of left ventriCulaR gene Expression (TRANSCRibE)
Clinical Cohort
2018-08-31
phs001680
Defining T cell States Associated with Response to Checkpoint Immunotherapy in Melanoma
Cohort
2018-09-04
phs001682
NHLBI TOPMed: Pulmonary Hypertension and the Hypoxic Response in SCD (PUSH)
Case-Control
2021-07-29
phs001683
Clinical Sequencing Exploratory Research Consortium: Incorporation of Genomic Sequencing into Pediatric Cancer Care
Longitudinal
2020-07-06
phs001684
Metatranscriptomic Sequencing of Pulmonary Fluid in Immunocompromised Children
Case Set
2018-09-06
phs001685
Prediction of DNA Repair Inhibitor Response in Short Term Patient-Derived Ovarian Cancer Organoids
Case Set
2018-09-07
phs001686
IL-17 Signaling in Human iPSC-derived Midbrain Neurons in Parkinson's Disease
Case-Control
2018-09-07
phs001687
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Case-Control
2018-09-07
phs001688
Microarray Gene Expression Data from Early Skin Biopsies of a Secukinumab Clinical Trial in Psoriasis
Randomized Controlled Clinical Trial
2018-09-10
phs001689
Multiethnic Cohort Adiposity Phenotype Study (MEC-APS)
Cross-Sectional
2018-09-11
phs001690
Somatic Copy Number Analysis of Endometrial Carcinomas
Case Set
2018-09-11
phs001691
Genetic Etiology of Heterotaxy
Case Set
2018-09-12
phs001692
Lifestyle, Infertility, Fertility, and Evaluation (LIFE) Study
Cohort
2018-09-19
phs001693
Maternal-Fetal Immune Responses in Preterm Labor and Congenital Anomalies
Cohort
2018-09-19
phs001694
Cerebrospinal Fluid Analysis of HIV-1 Viral Burden in HIV-1 Infected Subjects: Response to Antiretroviral Therapy
Cohort
2018-09-19
phs001695
UCSF Center for Reproductive Health (CRH) Research Bank
Cohort
2018-09-19
phs001696
Genomic Studies for Understanding Etiology of Esophageal Adenocarcinoma (EsophagealAdenocarcinoma_Chinese)
Case Set
2018-09-20
phs001697
Integrative Analysis of Lung Adenocarcinoma in Never Smokers
Case Set
2018-09-20
phs001698
Stanford Center for Urologic Genomics: Genomic Analysis of Benign Prostatic Hyperplasia
Case Set
2018-09-20
phs001699
Germline DNA Methylation Associated with Breast Cancer Predisposition
Case-Control
2018-09-20
phs001700
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Case Set
2018-09-25
phs001701
INdiana GENomics: Implementing an Opportunity for the Under Served (INGENIOUS)
Cohort
2018-09-27
phs001702
In Vivo Cytokine eQTL Interactions from a Lupus Clinical Trial
Cohort
2018-09-28
phs001703
Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression
Longitudinal Cohort
2021-03-05
phs001704
Enhancer Mapping in Chronic Lymphocytic Leukemia
Case-Control
2018-10-01
phs001705
National Cancer Institute - Population Structure and Natural Selection in the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) study in Uganda
Case-Control
2018-10-01
phs001706
Idiopathic Multicentric Castleman Disease Whole Genome Sequencing Project
Cohort
2018-10-04
phs001707
University of Pennsylvania CAR T Cell Responding and Non-responding Patients
Cohort
2020-01-27
phs001709
Count Me In (CMI): The Metastatic Breast Cancer (MBC) Project (CMI-MBCproject)
Cohort
2018-10-04
phs001710
Transplant Outcomes in Aplastic Anemia (TOAA): GWAS and WES Data
Cohort
2018-10-04
phs001711
Single-Cell Genome Sequencing of Gastrointestinal Carcinomas
Case Set
2018-10-11
phs001712
VCRC Genetic Repository One Time DNA Protocol
Case-Control
2018-10-12
phs001713
LCCC 1108: Development of a Tumor Molecular Analyses Program and Its Use to Support Treatment Decisions (UNCseqTM)
Cohort
2018-10-12
phs001714
Gabriella Miller Kids First Pediatric Research Program: An Integrated Clinical and Genomic Analysis of Treatment Failure in Pediatric Osteosarcoma
Tumor vs. Matched-Normal
2018-10-15
phs001715
VCRC Imaging Protocol for Magnetic Resonance and Positron Emission Tomography in Large-Vessel Vasculitis (Takayasu's Arteritis): Development as Clinical Trial Outcome Measures Vasculitis Clinical Research Consortium
Longitudinal
2018-10-15
phs001717
Genetic Variants Influence on the Placenta Regulatory Landscape
Control Set
2018-10-16
phs001718
C9ORF72 Hexanucleotide Repeat Sequence Genotyping Project
Cohort
2018-10-17
phs001719
Integrated Personal omics Processing (iPoP) Longitudinal multi-omics profiling of prediabetes
Longitudinal Cohort
2018-10-17
phs001720
Genome-wide chromatin accessibility profiling of primary human glomerular and kidney cortex tubular outgrowth cultures
Collection
2018-10-19
phs001721
NIDDK IBD Genetics Consortium Repository Immunochip
Case-Control
2018-10-23
phs001722
Understanding the Progression of Metastatic Colorectal Cancer
Cohort
2018-10-23
phs001723
NIDDK IBD Genetics Consortium Repository Exome Chip
Case-Control
2018-10-23
phs001724
Genomics and Modification of Pain: A peripheral component identified using iPSCs with the S241T mutation
Parent-Offspring Trios
2018-10-23
phs001725
NHLBI TOPMed - NHGRI CCDG: Groningen Genetics of Atrial Fibrillation (GGAF) Study
Cohort
2021-07-29
phs001726
NHLBI TOPMed: Childhood Asthma Management Program (CAMP)
Parent-Offspring Trios
2020-10-08
phs001727
NHLBI TOPMed: Pathways to Immunologically Mediated Asthma (PIMA)
Cohort
2021-08-11
phs001728
NHLBI TOPMed: Best ADd-on Therapy Giving Effective Response (BADGER)
Cohort
2021-08-11
phs001729
NHLBI TOPMed: Characterizing the Response to a Leukotriene Receptor Antagonist and an Inhaled Corticosteroid (CLIC)
Cohort
2021-08-11
phs001730
NHLBI TOPMed: Pediatric Asthma Controller Trial (PACT)
Cohort
2021-08-11
phs001732
NHLBI TOPMed: TReating Children to Prevent EXacerbations of Asthma (TREXA)
Cohort
2021-08-11
phs001733
Molecular Etiology of Early-Onset Dystonia
Cohort
2018-10-26
phs001734
Youth Drug Abuse, ADHD and Related Disorders
Cohort
2018-10-26
phs001735
NHLBI TOPMed: Pediatric Cardiac Genomics Consortium (PCGC)'s Congenital Heart Disease Biobank
Case Set
2021-01-06
phs001736
NCI Expanded Genome-Wide Association Study of Renal Cell Carcinoma
Case Set
2022-03-25
phs001737
The epigenetic landscape controlled by p63 in epidermal development
Case-Control
2019-07-25
phs001738
Kids First Pediatric Research Study in Familial Predisposition to Hematopoietic Malignancies (SJFAMILY-HM)
Cohort
2018-11-06
phs001739
Role of the Cervico-Vaginal Microbiome in Spontaneous Preterm Birth
Longitudinal
2018-11-07
phs001740
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE)
Cohort
2018-11-13
phs001741
Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC)
Cohort
2018-11-13
phs001742
High-Resolution Clonal Mapping of Multi-Organ Metastasis, and Resistance to Neoadjuvant Chemotherapy, in Triple Negative Breast Cancer
Case-Control
2019-03-14
phs001743
Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis
Longitudinal Cohort
2018-11-13
phs001744
Genome-Wide Association Study of HCC in Non-Asian USA Population
Case-Control
2018-11-13
phs001745
Human Lung Tissue eQTL Study
Cohort
2018-11-15
phs001746
A Genomic Atlas of Systemic Interindividual Epigenetic Variation in Humans (GTEx)
Reference Set
2021-11-17
phs001747
Caregiving as a Natural Stressor in Studies of the Role of Genes That Affect Serotonin Function in Regulating Risk Factors for Coronary Heart Disease (CAREGIVER)
Case-Control
2018-11-27
phs001748
Molecular Genetics of Histiocytic Sarcoma
Case Set
2018-11-28
phs001749
Genetics of Congenital Anomalies of the Kidney and Urinary Tract
Case-Cohort
2021-04-05
phs001750
Single Cell Analysis of Pulmonary Fibrosis
Cohort
2018-11-30
phs001751
Rare Disease Susceptibility Variant Study in Children with Crohn's Disease and Their Parents Using Targeted Gene Sequencing.
Case-Control
2018-11-30
phs001752
Genomics and Methylation of Neuroendocrine Prostate Cancer from cfDNA (Cornell/Trento 2019)
Cohort
2018-12-12
phs001753
Rapid Evolution of a Skin Lightening Allele in Southern African KhoeSan
Cohort
2018-12-13
phs001754
Spit for Science
Longitudinal
2021-02-16
phs001758
Identification of Rare Germline Variants in Familial Patients with Non-medullary Thyroid Cancer
Case Set
2018-12-18
phs001759
Profiles of Extracellular RNA in Cerebrospinal Fluid and Plasma from Subarachnoid Hemorrhage Patients
Case Set
2018-12-20
phs001761
Genomic Characteristics of Myeloproliferative Neoplasms in Patients Exposed to Ionizing Radiation following the Chernobyl Nuclear Accident
Case-Control
2018-12-28
phs001765
Whole Exome Sequencing of Parathyroid Cancer Identifies Candidate Driver Mutations and Core Pathways
Cohort
2019-01-03
phs001766
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange
Family
2019-01-04
phs001767
Identifying Novel Small RNA Biomarkers Unique to Patients with Gastric Cancer
Case-Control
2019-01-04
phs001768
Longitudinal Assessment of Methylmercury and Gut Microbes During Pregnancy
Longitudinal
2019-01-09
phs001769
Safety and Efficacy of Intravenous Norepinephrine for Orthostatic Hypotension
Interventional
2019-01-10
phs001770
Assessment of Health-related Quality of Life in Rare Kidney Stones
Longitudinal
2019-01-10
phs001771
Genomic Diagnosis and Individualized Therapy of Highly Penetrant Genetic Diabetes
Longitudinal
2019-01-16
phs001772
A Genomic Approach to Improved Diagnosis and Treatment of Neuroendocrine Tumors
Case Set
2022-05-31
phs001774
University of Washington Center for Mendelian Genomics (UW-CMG): Atrioventricular Septal Defects (AVSD) Study
Mixed
2019-01-22
phs001775
Alcohol Dependence: Sequencing from Multiplex Families
Case-Control
2019-01-24
phs001776
NCI Laboratory of Translational Genomics (LTG) Human Pancreas QTL study
Genotype/Expression
2019-01-24
phs001777
Analysis of the Whole Transcriptomes of Human Testis with Complete Spermatogenesis and of Human Testes with Sertoli Cell-Only Syndrome
Case-Control
2019-01-25
phs001778
Myelodysplastic Syndrome (MDS) in Humanized Mice
Case Set
2019-01-25
phs001779
Center for Inherited Disease Research (CIDR)-National Institute on Aging (NIA) Whole Exome Analysis of Ehlers-Danlos Syndrome
Case-Control
2019-01-29
phs001780
African Demographic History Study Using Illumina 1M Array Data
Cohort
2019-01-31
phs001781
Proteogenomic Landscape of Squamous Cell Lung Cancer
Cohort
2019-02-04
phs001782
Effect of the Placental Transcriptome on Stunting in a Longitudinal African Cohort
Longitudinal
2021-06-14
phs001783
Exome Recapture and Sequencing of Prospectively Characterized Clinical Specimens From Cancer Patients
Case Set
2022-10-12
phs001784
Molecular Features of Hepatocellular Carcinoma Associated with 18F-Fluorocholine PET/CT Imaging Phenotype
Control Set
2019-02-08
phs001785
Gabriella Miller Kids First Pediatric Research Program for Infantile Hemangiomas Associated with Multi-Organ Structural Birth Defects
Cohort
2019-02-11
phs001786
Stand Up 2 Cancer (SU2C) Genomics-Enabled Medicine for Melanoma (GEMM) Trial
Case Set
2019-02-11
phs001787
Discovery of Colorectal Cancer Susceptibility Genes in High-Risk Families
Case Set
2019-02-20
phs001788
Centers for AIDS Research (CFAR) Network of Integrated Clinical Systems (CNICS)
Longitudinal
2019-02-20
phs001790
NIMH Human Middle Temporal Gyrus (MTG) Cell Types
RNA Sequencing
2019-03-06
phs001791
A Multimodal Atlas of Human Brain Cell Types
RNA Sequencing
2019-03-06
phs001792
Intergenerational Impact of Genetic and Psychological Factors on Blood Pressure (InterGEN Study)
Longitudinal Cohort
2019-03-06
phs001793
Pharmacogenomic Interactions in Glioblastoma Cell Line Models
Case Set
2019-03-07
phs001794
Beckwith-Wiedemann Syndrome (BWS) miRNA Data
Cohort
2019-03-11
phs001795
Genetic Analysis of the Chiari I Malformation
Case-Control
2019-03-12
phs001796
Correlates of Human Nerve Repair
Longitudinal Cohort
2019-03-13
phs001797
UW TAN Study of Metastatic Urothelial Carcinoma
Case Set
2019-03-18
phs001798
A New Reference Panel to Boost African American Genotype Imputation
Population Genomics
2021-05-17
phs001799
Genomic landscape of Neutrophilic Leukemias of Ambiguous Diagnosis
Cohort
2019-03-20
phs001800
Genomics of Pediatric Renal Medullary Carcinomas
Cohort
2020-11-10
phs001802
Genetics of Lymphatic Anomalies from Center of Applied Genomics (CAG) at CHOP
Cohort
2020-05-21
phs001803
Identification of Genomic Markers of Cervical Dystonia and Subtypes
Cohort
2019-03-28
phs001804
NIDA Genetic Epidemiology of Opioid Dependence in Bulgaria (GEODB)
Case Set
2019-04-01
phs001805
Endogenous CD4+ T Cells Recognize Neoantigens in Lung Cancer Patients, including KRAS and ERBB2 (Her2) Driver Mutations
Case Set
2019-04-03
phs001806
Kids First: Whole Genome Sequencing of Nonsyndromic Craniosynostosis
Cohort
2019-04-03
phs001807
InTEAM Consortium - Alcoholic Hepatitis
Case Set
2019-04-05
phs001808
Landscape of Somatic Mutations in B Lymphocytes Across Human Lifespan
Cross-Sectional
2019-04-08
phs001809
GSCAN GWAS Meta-analysis of Tobacco and Alcohol use (GSCAN-GWAS)
Meta-Analysis
2019-04-10
phs001810
Gene-Environment Interactions in COCCaINE Use Disorder: Collaborative Case-Control Initiative in Cocaine Addiction
Cohort
2022-07-28
phs001811
Molecular Determinants of Tumor Behavior in Early Lung Adenocarcinoma
Cohort
2019-04-15
phs001812
Genetic and Epigenetic Determinants of Pediatric Obesity-Associated Asthma
Case-Control
2019-04-16
phs001813
Integrative Tissue Analysis of Men with Prostate Cancer
Case Set
2022-04-21
phs001814
Molecular Genetics of Heterotaxy and Related Congenital Heart Defects
Case Set
2019-04-29
phs001815
Minority Health Genomics and Translational Research Bio-Repository Database
Case-Control
2019-04-29
phs001816
CRISPR-Mediated ASD Gene Knockout Reduces Neuronal Activity
Case-Control
2019-04-29
phs001817
GeneScreen, a Population Based, Targeted Genomic Screening Study
Cross-Sectional
2019-04-30
phs001818
Single-Cell Genomic Analysis of Gastrointestinal Cancer
Case Set
2020-08-31
phs001819
Whole Genome Sequencing to Discover Familial Myeloma Risk Genes
Case Set
2020-10-08
phs001820
The Institute for Genomic Medicine at Nationwide Children's Hospital Pediatric Cancer and Blood Disorder Project
Cohort
2022-02-02
phs001823
Molecular Biomarkers Predicting Lung Cancer Response Phenotypes
Cohort
2019-05-03
phs001824
RNASeq of Plasmacytoid Dendritic Cells in Head and Neck Squamous Cell Cancer Patients
Longitudinal Cohort
2019-05-06
phs001825
Study of 5'UTR Mutations in Prostate Cancer
Cohort
2019-05-07
phs001826
Mobile Technology to Identify Mechanisms Linking Genetic Variation and Depression in Intern Health Study (IHS)
Longitudinal Cohort
2019-05-10
phs001828
Genetic Studies of Chronic Kidney Disease (CKD)
Case Set
2019-05-20
phs001829
Molecular Characterization of Response to Rectal Chemoradiation
Case Set
2019-05-20
phs001830
Tumor heterogeneity and acquired drug resistance in FGFR2 fusion-positive cholangiocarcinoma through rapid research autopsy
Case Set
2019-05-21
phs001831
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Cohort
2019-05-23
phs001833
Genetic Model of MS Severity Predicts Future Accumulation of Disability
Cohort
2019-05-29
phs001834
Genetics of Fuchs Corneal Dystrophy
Case-Control
2019-05-30
phs001835
Whole-Exome Sequencing and Targeted DNA Sequencing of Matched Ocular Melanocytosis and Uveal Melanoma
Case Set
2019-05-31
phs001836
A Single Cell Transcriptomic Analysis of Human Neocortical Development
Cohort
2019-05-31
phs001837
The Intestinal Bacterial Metagenome in Pediatric Non-Alcoholic Fatty Liver Disease (NAFLD)
Case-Control
2019-06-03
phs001839
Deep Sequencing of 3 Cancer Cell Lines on 2 Sequencing Platforms (Illumina HiSeqX and NovaSeq)
Case Set
2019-06-04
phs001840
Cross-Species Single-Cell Analysis of Pancreatic Ductal Adenocarcinoma Reveals Antigen-Presenting Cancer-Associated Fibroblasts
Cohort
2019-06-06
phs001841
CADD/GADD centers on Antisocial Drug Dependence
Family
2019-06-06
phs001842
RNAseq of Sjögren's Syndrome and Healthy Volunteers' Salivary Glands
Case-Control
2019-06-06
phs001844
Genome-Wide Association of Type 2 Diabetes in Africans: The AADM Study
Case-Control
2019-06-07
phs001845
Transcriptomic Analysis of Human Hematopoietic Progenitors from Healthy Donors and Bone Marrow Failure Patients
Case-Control
2019-06-07
phs001846
Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects
Cohort
2019-06-11
phs001847
Characterization of Structural Variants in Acute Myeloid Leukemia Patients
Cohort
2019-06-11
phs001848
Human PI3Kγ Deficiency with Immunodeficiency and Tissue Immunopathology
Parent-Offspring Trios
2019-06-12
phs001849
RNA sequencing, ATACseq, and TCR-seq of Tfh cells and CXCR5- CD4+ T cells in HIV infected lymph nodes
Cohort
2019-06-17
phs001850
A Phenotypic and Genomics Approach in a Multi-Ethnic Cohort to Subtype Systemic Lupus Erythematosus
Prospective
2019-06-17
phs001851
The MALT1 Locus and Peanut Avoidance in the Risk for Peanut Allergy
Cohort
2019-06-21
phs001852
Analysis of the Genetic Basis of Height in Large Jewish Nuclear Families
Family
2019-06-21
phs001853
Liquid Biopsy Versus Tissue Biopsy to Assess Acquired Resistance and Tumor Heterogeneity in Gastrointestinal Cancers
Longitudinal Cohort
2019-06-21
phs001854
Human Pilocytic Astrocytoma Single Cell RNA Sequencing
Case Set
2019-06-25
phs001855
Studies of a Targeted Risk Reduction Intervention through Defined Exercise (STRRIDE)
Interventional
2019-06-27
phs001856
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS
Case-Control
2019-06-28
phs001857
Genetics of Mammographic Density in Ashkenazi Jews
Cross-Sectional
2019-07-01
phs001858
Anonymized germline variants of prospectively characterized clinical cancer specimens
Case Set
2019-07-01
phs001859
Genomic Characterization CS-MATCH-0007 Arm Z1D
Cohort
2019-07-03
phs001860
Genetics and Pathophysiology of Autoinflammatory Disorders
Parent-Offspring Trios
2019-07-05
phs001861
Single cell analysis reveals new evolutionary complexity in uveal melanoma
Case Set
2019-07-05
phs001862
Michigan Polybrominated Biphenyl (PBB) Exposure Registry
Cohort
2019-07-05
phs001863
Randomized Phase II 2 x 2 Factorial Trial of the Addition of Carboplatin +/- Bevacizumab to Neoadjuvant Weekly Paclitaxel Followed by Dose-Dense AC in Hormone Receptor-Poor/HER2-Negative Resectable Breast Cancer
Clinical Trial
2019-07-08
phs001864
MAP Kinase-Mutant Hematologic Malignancies and Their Therapeutic Resistance
Cohort
2019-07-09
phs001865
Emory University African American Vaginal, Oral, and Gut Microbiome in Pregnancy Cohort Study
Cohort
2019-07-09
phs001866
RNA Sequence-Based Analysis Used to Compare Breast Primary and Metastatic Tumor Pairs
Cohort
2019-07-12
phs001867
Detection of Somatic Mutations In Vitro Aging Cells
Population
2019-07-15
phs001868
Cutaneous Melanoma GWAS Combining Multiple Populations and Risk Phenotypes
Case-Control
2019-07-16
phs001869
ADHD Genomic Association Study
Case-Control
2019-07-17
phs001870
Genomic Changes in Breast Cancer Among Chinese Women in Hong Kong
Case Set
2019-07-25
phs001871
Center for Common Disease Genomics (CCDG) - Cardiovascular: Cleveland Clinic Cohort
Case-Control
2019-07-26
phs001872
Genome Sequencing of Large, Multigenerational CEPH/Utah Families
Cohort
2019-07-30
phs001874
Nature and Contribution of Noncoding, Regulatory Mutations in Neurodevelopmental Disorders
Case-Control
2019-07-31
phs001875
Determinants of Venetoclax Resistance
Longitudinal
2019-07-31
phs001876
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders
Case-Control
2019-08-01
phs001877
Genetics of Cutaneous T-Cell Lymphoma
Case-Control
2019-08-01
phs001879
Microbiota and Complications in Kidney Transplant Recipients
Cohort
2019-08-07
phs001880
Center for Common Disease Genomics (CCDG) - Cardiovascular: Emory Cohort
Case-Control
2019-08-12
phs001881
A Large Data Resource of Genomic Copy Number Variation across Neurodevelopmental Disorders
Case-Control
2019-08-14
phs001882
OncoArray: Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Case-Control
2019-08-14
phs001883
Whole Exome Sequencing of DNA from Pre-and Post-Chemotherapy Needle Biopsies of Triple Negative and Inflammatory Breast Cancers Enrolled in the S0800 Trial
Clinical Trial
2019-08-15
phs001884
The Etiological Bases of Giftedness: Epidemiological Study of Cognitive Ability in Children in Saudi Arabia
Cohort
2019-08-15
phs001885
Endometrial Cancer Association Consortium - OncoArray Genotypes
Case Set
2019-08-19
phs001886
Deciphering Maternal-Fetal Crosstalk in the Human Placenta During Parturition Using Single-Cell RNA-Sequencing
Case-Control
2022-03-03
phs001887
Single-Sperm Genome Sequencing of Sperm Donors
Cohort
2019-08-20
phs001888
Genomic Characterization CS-MATCH-0007 Arm H
Cohort
2019-08-21
phs001889
Transposable Elements in FTLD-TDP and ALS-TDP
Case-Control
2019-08-22
phs001890
Single molecule molecular inversion probe capture developed using the CIViC database
Tumor vs. Matched-Normal
2019-08-26
phs001892
miRNA Profiling of Maternal and Non-Maternal Healthy Adult Blood Plasma Using Small RNA-Sequencing
Case-Control
2019-08-28
phs001894
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Family
2019-09-04
phs001895
Enrichment of PTPRT and JAK2 mutations in lung cancer from African Americans and evidence for increased GI and HRD in LUSC
Case-Control
2019-12-06
phs001896
Etiologic Studies of Macular Degeneration
Case-Control
2019-09-10
phs001897
Regulatory and Effector T cells in Oral Immunotherapy for Food Allergy
Randomized Controlled Clinical Trial
2022-02-28
phs001898
Invariant patterns of clonal succession determine specific clinical features of Myelodysplastic syndromes (MDS)
Case Set
2019-09-13
phs001899
NIAID Centralized Sequencing Program
Mixed
2020-09-02
phs001900
Genetic Control of Expression and Splicing in Developing Human Brain
Cohort
2019-09-18
phs001901
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetics of Coronary Heart Disease - Characterizaton of Coronary Prone Pedigrees
Case-Control
2019-09-19
phs001902
Whole Exome Sequencing Study of TGFΒ Pathway Genes in HCV Liver Fibrosis
Case-Control
2019-09-20
phs001903
dbGaP submission of CORECT OncoArray GWAS data
Case-Control
2019-09-23
phs001904
Genomic Characterization CS-MATCH-0007 Arm Y
Cohort
2019-09-25
phs001905
CIDR: Molecular Pathological Epidemiology of Colorectal Cancer
Case Set
2019-09-26
phs001906
Altered chromosomal topology drives oncogenic programs in gastrointestinal stromal tumors
Case Set
2019-09-26
phs001907
CPTAC: Microscaled Proteogenomic Methods for Precision Oncology
Cohort
2019-09-27
phs001908
Spatiotemporal Analysis of the Human Cerebellum
Control Set
2021-02-23
phs001909
The Vaginal Microbiome in Reproductive Age Women
Cross-Sectional
2019-10-01
phs001910
Enhancer signatures stratify and predict outcomes of non-functional pancreatic neuroendocrine tumors
Case Set
2019-10-03
phs001911
Identifying novel DNA damage response genes in radiosensitive individuals
Case Set
2019-10-03
phs001912
Somatic Genome Dynamics of Barrett's Esophagus Patients with Non-Cancer and Cancer Outcomes
Case-Control
2019-10-03
phs001913
Center for Common Disease Genomics (CCDG) - Cardiovascular: eMERGE - Northwestern Cohort
Case-Control
2019-10-03
phs001914
Improved Detection and Identification of Microsatellite Instability Features in Colorectal Cancer
Case-Control
2019-10-03
phs001916
Pilot Sequencing Study: DNA Hydroxymethylation and Gene Expression in Peripheral Blood Mononuclear Cells in Healthy Human Aging
Case-Control
2020-04-02
phs001917
DNA Methylation Markers and Pancreatic Cancer Risk in 3 Cohort Studies (NHS, PHS, HPFS)
Nested Case-Control
2019-10-10
phs001918
STAMPEED: Whole Genome Association Analysis of Hematopoietic Cell Transplant (HCT) Outcomes
Cohort
2021-09-27
phs001919
PAK4 inhibition improves PD-1 blockade immunotherapy
Cohort
2019-10-16
phs001920
Genomic Characterization of Brain Metastases from Lung Cancer
Cohort
2019-10-16
phs001921
Primary Prostate Tumor Tissue DNA Methylation Profiles
Cohort
2019-10-20
phs001922
Chromosome Errors in Human Eggs and Natural Fertility
Case Set
2019-10-23
phs001924
Case Study of Acquired Resistance to FGFR Inhibition in Cholangiocarcinoma using Targeted DNA and RNA Sequencing
Case Set
2019-10-25
phs001925
Characterization of Clonal Evolution in Microsatellite Unstable Metastatic Cancers through Multi-Regional Tumor Sequencing
Case Set
2019-11-01
phs001927
NHLBI TOPMed: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS)
Cohort
2019-11-05
phs001928
A Comprehensive Genomic Study of Pediatric Malignancy
Cohort
2019-11-07
phs001929
Neurogenetic Investigations of Obsessive-Compulsive Disorder
Parent-Offspring Trios
2019-11-08
phs001930
Mechanism of Action of Vitamin E in NAFLD
Clinical Trial
2019-11-12
phs001931
Count Me In (CMI): The Angiosarcoma (ASC) Project (CMI-ASCproject)
Cohort
2019-11-14
phs001932
RNAseq Transcriptomic Analyses of European Ancestry Samples in MGS Dataset
Case-Control
2019-11-14
phs001933
NHLBI TOPMed - NHGRI CCDG: UCSF Atrial Fibrillation Study
Case Set
2019-11-19
phs001934
Sexual dimorphism in human immune system aging
Cross-Sectional
2019-11-20
phs001935
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Case Set
2019-11-21
phs001936
Extent and Significance of Bacterial DNA Integrations in the Human Cancer Genome
Case Set
2019-11-21
phs001937
DNA Methylomic Profiling of Preeclampsia Across Pregnancy
Longitudinal
2019-11-21
phs001938
Genomic and Genetic Characterization of Prostate Tumors Treated with Neoadjuvant Intense Androgen Deprivation Therapy
Case Set
2021-09-01
phs001939
Count Me In (CMI): The Metastatic Prostate Cancer (MPC) Project (CMI-MPCproject)
Cohort
2022-03-07
phs001940
Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer
Cohort
2020-01-30
phs001941
NIDCD Otitis Media Genetic Susceptibility and Middle Ear Microbial Shifts
Family
2022-02-18
phs001942
Molecular Genetics of Secondary Histiocytic/Dendritic Sarcoma
Case Set
2019-12-02
phs001943
Hereditary Cancer Predisposition Syndromes and Uveal Melanoma
Cohort
2019-12-03
phs001945
National Institutes of Health H3Africa African Collaborative Center for Microbiome and Genomics Research (ACCME)
Longitudinal
2019-12-09
phs001946
Genetic Evaluation of Autoinflammatory Diseases
Cross-Sectional
2019-12-10
phs001947
Whole Transcriptome Sequencing of Resectable Stage III/IV Melanoma Evaluated After Starting Hu14.18-IL2 Predicts Outcome
Cohort
2019-12-11
phs001948
Genomic Characterization CS-MATCH-0007 Arm W
Cohort
2019-12-11
phs001949
Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants
Case-Control
2019-12-13
phs001951
Relapsed Acute Lymphoblastic Leukemia (ALL): Mutational Landscape
Longitudinal
2022-01-21
phs001953
Genomic profiling for metastatic uveal melanoma from a phase I study of the protein kinase C inhibitor AEB071
Clinical Trial
2019-12-24
phs001954
International Cancer Proteogenome Consortium (ICPC): proteogenomics of early stage lung adenocarcinoma in Taiwan
Case Set
2019-12-24
phs001955
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Red Blood Cell Omics (RBC-Omics) Study
Cohort
2019-12-27
phs001956
Single-cell analysis reveals different age-related somatic mutation profiles between stem and differentiated cells in human liver
Cross-Sectional
2019-12-27
phs001957
Investigation of Human DNA Replication Timing Variation by Whole Genome Sequencing
Cohort
2021-05-13
phs001958
Cell-Type Specific Effects of Genetic Variation on Chromatin Accessibility During Human Neuronal Differentiation
Cohort
2020-01-02
phs001959
Nanopore cDNA Sequencing of Chronic Lymphocytic Leukemia
Case-Control
2020-01-02
phs001960
Epigenome Wide DNA Methylation Study for Osteoporosis Risk
Case-Control
2020-01-07
phs001961
LungMAP: Molecular Atlas of Lung Development - Human Lung Tissue
Longitudinal
2022-10-21
phs001962
Genomic Profiling of Peripheral T-cell Lymphoma
Cohort
2020-01-13
phs001963
DEMENTIA-SEQ: WGS in Lewy Body Dementia and Frontotemporal Dementia
Case-Control
2021-07-07
phs001964
Women's Health Study Accelerometry Dataset
Longitudinal
2020-01-14
phs001965
MP2PRT: Identification of Genetic Changes Associated with Relapse and/or Adaptive Resistance in Patients Registered as Favorable Histology Wilms Tumor on AREN03B2
Case Set
2020-01-14
phs001966
L1 Retrotransposon sequencing in Cocaine Use Disorder - Study 1
Case-Control
2020-01-28
phs001967
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Case Set
2020-01-29
phs001968
L1 Retrotransposon Sequencing in Schizophrenia - Study 1
Case-Control
2020-01-29
phs001969
Cellular Origins and Genetic Landscape of Cutaneous GD T Cell Lymphoma
Case Set
2020-01-30
phs001970
DNA Methylation Characterization of Fusion-Positive and Fusion-Negative Rhabdomyosarcoma
Case Set
2020-01-30
phs001971
Kidney Two-Hit Mapping
Case Set
2020-01-31
phs001972
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Cohort
2020-01-31
phs001973
Genomic Characterization CS-MATCH-0007 Arm Z1A
Cohort
2020-01-31
phs001974
NHLBI TOPMed: Genomic Summary Results for the Trans-Omics for Precision Medicine Program
Case Set
2023-02-23
phs001975
SNP array analysis of spondylocostal dysostosis patient iPSCs and gene edited isogenic controls
Case-Control
2020-02-05
phs001976
Natural History, Pathogenesis and Outcome of Melorheostosis
Longitudinal
2020-03-26
phs001977
Large Cancer Fingerprint Screening for Detection of Minimal Residual Disease.
Case-Control
2020-02-10
phs001978
IGNITE: Implementing GeNomics In practice: Genomic Medicine Implementation - The Personalized Medicine Program
Clinical Trial
2020-02-13
phs001979
Genomic Landscape of Human Skin at a Single-Cell Resolution
Cross-Sectional
2020-02-13
phs001980
University of Texas PDX Development and Trial Center Grant
Cohort
2021-12-02
phs001981
National Institute on Alcohol Abuse and Alcoholism (NIAAA) Postmortem Prefrontal Cortex eQTL and mQTL Study
Case-Control
2020-02-18
phs001982
Rb and p53-Deficient Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma Require Skp2 for Survival
Case Set
2020-02-24
phs001983
HTAN Pilot Project: Single-Cell Transcriptomics Toolbox for Fresh and Frozen Human Tumors (Lung, Breast, Ovarian, Melanoma, Neuroblastoma, Sarcoma, Glioblastoma, Glioma, and Leukemia)
Case Set
2020-02-26
phs001984
GWAS for Membranous Nephropathy
Case-Control
2020-02-27
phs001987
Gabriella Miller Kids First Pediatric Research Program in Enchondromatoses and Related Malignant Tumors
Cohort
2022-09-20
phs001988
Molecular Characterization of Prostate Cancer Specimens by Bulk and Single Cell Analysis
Case Set
2020-03-03
phs001990
Epigenomics of Patient Outcomes after Aneurysmal SAH
Longitudinal
2020-03-05
phs001991
dbGaP Collection: NHLBI Heart Failure Related dbGaP Data (No IRB requirement)
Collection
2020-03-06
phs001992
A panel of reference haplotypes for imputing complement component 4 (C4) gene structural variation
Cohort
2020-03-10
phs001993
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas
Cohort
2020-03-11
phs001994
Effects of tobacco smoking on the tumor immune microenvironment in head and neck squamous cell carcinoma
Cohort
2020-03-13
phs001995
Capturing the genetic diversity of the Himba population
Family
2020-03-17
phs001997
Gabriella Miller Kids First Pediatric Research Program in Whole Genome Sequencing of African and Asian Orofacial Clefts Case-Parent Triads
Cohort
2020-03-20
phs001998
Evolutionary Analysis of Chronic Lymphocytic Leukemia Cells During Relapse After Allogeneic Hematopoietic Stem Cell Transplant
Case Set
2020-03-23
phs001999
Advanced Genetic and Molecular Analysis of Solid Tumors
Case-Control
2020-03-25
phs002000
The Genomic Landscape of Mongolian Hepatocellular Carcinoma
Case Set
2020-03-25
phs002001
Clonal Evolution and Heterogeneity of Osimertinib Acquired Resistance Mechanisms in EGFR Mutant Lung Cancer
Longitudinal
2020-03-27
phs002002
Landscape of Intratumoral NK Cell and ILC in Head and Neck Squamous Cell Carcinoma
Case Set
2020-03-31
phs002003
University of Washington Developmental Single Cell Atlas
Control Set
2020-04-01
phs002004
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Family
2020-04-02
phs002005
MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features
Case-Control
2020-04-04
phs002006
Segmental Overgrowth/Vascular Anomalies/Dermatologic Disorders
Case Set
2020-08-05
phs002007
Transcriptomic Characterization of Human Innate T Cells
Control Set
2020-04-07
phs002008
The Epigenomic Atlas of Early Human Craniofacial Development
Control Set
2020-04-09
phs002009
Genomic Landscape of Pediatric Germ Cell Tumors
Case Set
2020-04-14
phs002010
The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD)
Case Set
2020-04-14
phs002011
PLCO - Limited Use Pilot Test Data
Longitudinal
2020-04-14
phs002012
SEER Remote Access Pilot Test Data (2018)
Methods Development
2020-04-14
phs002015
National Eye Institute (NEI) Age-Related Eye Disease Study 2 (AREDS2)
Case Set
2021-02-26
phs002016
MicroRNA Biomarkers for Prediction of Preeclampsia
Case-Control
2020-04-17
phs002017
Circulating RNA profiles of healthy and preeclamptic pregnancies
Case-Control
2020-04-17
phs002018
Center Common Disease Genomics [CCDG] - Cardiovascular: Partners Biobank
Case-Control
2020-04-21
phs002019
Whole exome and transcriptome analysis of UV-exposed epidermis and carcinoma in situ reveals early drivers of carcinogenesis
Case Set
2020-04-22
phs002020
Clinical and genetic analysis of retinopathy of prematurity - GWAS
Longitudinal
2020-04-23
phs002021
Phase II trial of targeted immune-depleting chemotherapy and reduced-intensity allogeneic hematopoietic stem cell transplantation using 8/8 and 7/8 HLA-matched unrelated donors and utilizing two graft-versus-host disease prophylaxis regimens for the treatment of leukemias, lymphomas, and pre-malignant blood disorders
Clinical Trial
2020-04-23
phs002022
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Cohort
2020-04-23
phs002023
Drug screening of patient-derived organoids from colorectal peritoneal metastases
Cohort
2020-04-29
phs002024
DCCT/EDIC Epigenetics (DNA Methylation) Study
Cohort
2020-04-30
phs002025
Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians
Case-Control
2020-05-06
phs002027
Induction of HIV-1 Env-Specific Peripheral Blood Plasmablasts and Clonal Persistence as Bone Marrow Plasma Cells Following Vaccination in Humans
Longitudinal
2021-11-24
phs002028
Genomic Characterization CS-MATCH-0007 Arm B
Cohort
2020-05-14
phs002029
Genomic Characterization CS-MATCH-0007 Arm R
Cohort
2020-05-14
phs002030
Impact of Mobile Element Insertions on Human Transcriptome Variation
Reference Set
2020-05-14
phs002031
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Control Set
2020-05-15
phs002032
Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes
Case-Control
2020-05-15
phs002033
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Cohort
2021-11-03
phs002034
Genomic Evolution of Low- and High-Grade Glioma
Longitudinal
2020-05-20
phs002035
National Heart, Lung and Blood Institute: Regulation of Motile Cilia Assembly in Lung Disease
Case Set
2020-05-26
phs002036
Chromoanasynthesis as a Cause of Jacobsen Syndrome
Case Set
2020-05-26
phs002037
Methylation biomarker study of magnesium deficiency and colorectal cancer
Randomized
2020-05-26
phs002039
Single-cell analysis of upper airway cells reveals host-viral dynamics in influenza infected adults
Cohort
2020-05-27
phs002040
Homozygous IL37 mutation leads to infantile inflammatory bowel disease
Parent-Offspring Trios
2020-05-28
phs002041
WGSPD Project 1: Whole Genome Sequencing for Schizophrenia and Bipolar Disorder
Case-Control
2020-05-29
phs002042
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
Family
2020-06-01
phs002043
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females
Parent-Offspring Trios
2020-06-01
phs002044
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder
Family
2020-06-04
phs002045
Intraductal transplantation models of human pancreatic ductal adenocarcinoma reveal progressive transition of molecular subtypes
Case Set
2020-06-04
phs002046
Grady Trauma Project (GTP)
Case-Control
2020-06-05
phs002047
Clinical and Genetic Analysis of Retinopathy of Prematurity (ROP)
Case-Control
2020-06-10
phs002048
Mapping Systemic Lupus Erythematosus Heterogeneity at the Single Cell Level
Case-Control
2021-03-12
phs002049
Memorial Sloan Kettering (MSKCC) Single Cell Mutational Profiling in Myeloid Malignancies
Cohort
2020-06-17
phs002050
OICR: Molecular Pathological Epidemiology of Colorectal Cancer
Case Set
2021-03-11
phs002051
DNA methylation in rhabdomyosarcoma PDX and PDX-derived primary cells
Case Set
2020-06-23
phs002052
Mitochondrial DNA deletion detection in POLG patients
Case-Control
2020-06-24
phs002053
Neoadjuvant Pazopanib in Renal Cell Carcinoma
Prospective
2020-06-25
phs002054
Genomic characterization of 9p- syndrome
Case Set
2020-06-26
phs002055
Peripheral Blood Transcriptome Analysis of ALS Patients
Case Set
2020-06-26
phs002056
Genetic Factors associated with Conversion from Active Surveillance to Treatment for Prostate Cancer
Case Set
2020-06-30
phs002057
Systems genetics in human endothelial cells identifies non-coding variants modifying enhancers, expression, and complex disease traits
Control Set
2020-06-30
phs002058
Genomic Characterization CS-MATCH-0007 Arm Z1I
Cohort
2020-07-02
phs002059
Genes for Non-Syndromic Congenital Heart Disease
Case Set
2020-07-06
phs002060
Pharmacogenomic Analysis of Microtubule Targeting Agent Response and Toxicity
Cohort
2020-07-09
phs002061
The Surveillance Monitoring for ART Toxicities (SMARTT) and the Women and Infants Transmission Study (WITS)
Cohort
2020-07-15
phs002062
Polygenic Risk Score for the Prediction of Breast Cancer Is Related to Lesser Terminal Duct Lobular Unit Involution of the Breast
Cross-Sectional
2020-07-15
phs002063
Innate and Adaptive Immunity in Parkinson Disease-P20
Case-Control
2020-07-15
phs002064
Metagenomic Analysis to Identify Novel Infectious Agents in Systemic Anaplastic Large Cell Lymphoma
Case-Control
2020-07-15
phs002065
Integrative Somatic and Germline Molecular Characterization of Genitourinary Cancers
Case-Control
2020-07-17
phs002066
Mechanisms of Extreme Genomic Instability at Large Transcribed Genes
Case-Control
2021-06-10
phs002067
Temporal Lobe Epilepsy and Retrotransposons
Case-Control
2020-07-20
phs002068
Sporadic ALS Australia Systems Genomics Consortium (SALSA-SGC)
Case-Control
2020-07-20
phs002069
Brain Arteriovenous Malformation Genetics Study
Case Set
2020-07-23
phs002070
Genomic Landscape of High-Grade Neuroendocrine Neoplasms
Cohort
2020-07-24
phs002071
Multimodal Mapping of the Immune Landscape in Human Pancreatic Cancer
Cohort
2020-07-30
phs002073
Effect of Breast Feeding on Immunologic Priming in Young Infants
Case-Control
2020-08-04
phs002075
Fetal Chorioamniotic Membranes Show Molecular Changes in Placenta Previa and Placenta Accreta Spectrum
Cohort
2020-08-04
phs002083
Role of Tobacco Smoke in Clear Cell Renal Cell Carcinoma
Cohort
2020-08-12
phs002088
Drug Signatures for Prediction and Mitigation of Toxicity
Control Set
2021-06-04
phs002089
Dynamics of Genomic and Immune Responses During Primary Immunotherapy Resistance in Mismatch Repair Deficient Tumors
Case Set
2020-08-13
phs002093
NSIGHT BabySeq Project
Case-Control
2020-08-14
phs002094
Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2)
Clinical Trial
2020-08-14
phs002095
NSIGHT North Carolina Newborn Exome Sequencing for Universal Screening (NC NEXUS)
Clinical Trial
2020-08-14
phs002097
Refractory Cancer (RC) Program
Case Set
2020-08-14
phs002102
Bone Microarchitecture
Cohort
2020-08-14
phs002105
Genomics of Opioid Pharmacogenomics and Acute/Chronic Postsurgical Pain after Major Surgery in Children
Longitudinal Cohort
2020-08-14
phs002106
Epigenetic Mechanisms of Inflammation and Fatigue in Head and Neck Cancer
Clinical Cohort
2020-08-14
phs002116
Unraveling the Genetic Architecture of Diabetic Retinopathy in South India
Case-Control
2020-08-14
phs002120
Center for Sub-Cellular Genomics
Single Cell Analysis
2020-08-14
phs002121
Integrated Clinical and Transcriptomic Profiling to Characterize Disease Phenotype
Case-Control
2020-08-14
phs002123
Drop-BS: High-Throughput Single-Cell Bisulfite Sequencing on a Microfluidic Droplet Platform
Epigenetics
2023-01-06
phs002128
Identification and Molecular Characterization of Somatic Mutations in Malformations of Cortical Development
Case Set
2020-08-14
phs002130
Gabriella Miller Kids First Pediatric Research Program in Craniofacial Microsomia
Cohort
2020-08-14
phs002139
Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort)
Genotype
2020-08-14
phs002140
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Longitudinal Cohort
2020-08-14
phs002143
Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation
Methods Development
2020-08-14
phs002146
Evolution of Chromatin Architecture and Transcriptional Regulation in Mammals
None
2020-08-14
phs002151
Genomic Characterization CS-MATCH-0007 Arm N
Cohort
2020-08-14
phs002153
Genomic Characterization CS-MATCH-0007 Arm S1
Cohort
2020-08-14
phs002156
Molecular Characterization of Hemimegalencephaly
Case Set
2020-08-14
phs002161
Kids First: Genomic Analysis of Esophageal Atresia and Tracheoesophageal Fistulas and Associated Congenital Anomalies
Cohort
2020-08-14
phs002162
Kids First: Genetics of Kidney and Urinary Tract Malformations
Cohort
2021-09-02
phs002164
Translating Gene-Calcium Interactions to Precision Medicine for Colorectal Cancer
Case-Control
2020-08-14
phs002170
Genome-Wide Association Study of Patients with Coccidioidomycosis
GWAS
2020-08-14
phs002171
Serrated Colorectal Cancer: An Emerging Disease Subtype
Case Set
2020-08-14
phs002172
Gabriella Miller Kids First Pediatric Research Project in Microtia in Hispanic Populations
Cohort
2020-08-14
phs002173
Gabriella Miller Kids First Pediatric Research Program in Bladder Exstrophy, Epispadias, Complex (BEEC)
Cohort
2020-08-14
phs002174
Gabriella Miller Kids First Pediatric Research Project in Cornelia de Lange Syndrome, Related Diagnosis and Structural Birth Defects
Cohort
2020-08-14
phs002176
Notch Signaling and Efficacy PD-1/PD-L1 Blockade in Relapsed Small Cell Lung Cancer
Clinical Trial
2021-05-07
phs002178
Genomic Characterization CS-MATCH-0007 Arm S2
Cohort
2020-08-14
phs002179
Genomic Characterization CS-MATCH-0007 Arm U
Cohort
2020-08-14
phs002181
Genomic Characterization CS-MATCH-0007 Arm I
Cohort
2020-08-14
phs002182
Asthma in the Lives of Families Today (ALOFT)
Cohort
2023-04-12
phs002183
The Multiethnic Cohort (MEC) Study
None
2020-08-14
phs002185
Genome-Wide Association Study of Genetic Susceptibility for Graft-vs-Host Disease Cohort 1
Cohort
2020-08-14
phs002187
Gabriella Miller Kids First Pediatric Research Program in Germline and Somatic Variants in Myeloid Malignancies in Children
Cohort
2020-08-14
phs002188
Single Cell Genomic Analysis of Lymphoma
Single Cell Analysis
2022-11-21
phs002189
Merkel Cell Carcinoma Tissue and Data Repository
Full Transcriptome Sequencing
2020-08-14
phs002192
Cancer Moonshot Biobank
Longitudinal
2020-08-14
phs002193
The Gut Microbiome in Parkinson's Disease
Nested Case-Control
2020-08-14
phs002196
Systems Analysis of the PfSPZ Vaccine in Kenyan Infants
Interventional
2020-08-14
phs002197
Single Cell and Tissue Level Functional Genomics Analysis of Astrocyte-Related Mechanisms in Taupathy
RNA Sequencing
2020-08-14
phs002202
A New High-Throughput Sequencing-Based Technology to Study Heterochromatin Structure
Control Set
2020-08-14
phs002203
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Cohort
2020-08-14
phs002204
A Single Cell Atlas of Gene Regulatory Elements in the Human Heart
Control Set
2020-08-14
phs002205
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Longitudinal
2020-08-14
phs002206
Genomic Answers for Kids (GA4K)
Case Set
2022-11-01
phs002207
Genomic and Transcriptomic Profiling of Patients with Malignant Pleural and Peritoneal Mesothelioma: The NCI Cohort
Case Set
2023-04-03
phs002208
Metatranscriptomic Sequencing of Pre-Transplant Bronchoalveolar Lavage in Pediatric Stem Cell Transplant Patients
None
2020-08-14
phs002210
Comprehensive Analysis of Structural Variants in Breast Cancer Genomes Using Single Molecule Sequencing
Case Set
2020-08-14
phs002211
Gynecology and Lubricant Effects (GALE) Study
Cohort
2020-08-14
phs002212
ZRSR2 Mutant Myelodysplastic Syndromes
Case Set
2020-08-14
phs002217
Single Cell ATAC-Seq of MELAS
Case Set
2020-08-14
phs002219
Genetic Study of Present-Day Populations of Northern Kenya
Cohort
2020-08-14
phs002220
Discovering the Genetic Basis of Cleft Palate: CIDR
Parent-Offspring Trios
2020-08-14
phs002221
Genetic Modifiers of Syndromic Orofacial Clefts
Whole Genome Sequencing
2020-08-14
phs002222
Transcriptomic and Clonal Characterization of T Cells in the Human Central Nervous System
Case-Control
2023-07-07
phs002224
Sputum RNA-Seq from Asthmatic Patients for Microbes and Genes
Cross-Sectional
2020-08-18
phs002225
HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study
Case Set
2021-09-28
phs002226
Multicenter AIDS Cohort Study (MACS)
Cohort
2020-08-19
phs002227
NeuroCHARGE Consortium GWAS of White Matter Hyperintensities on MRI
Cohort
2020-08-24
phs002228
Innate Immune Anti-Viral Deaminase Deregulation Fuels Pre-Leukemia Stem Cell Evolution
Case-Control
2023-01-09
phs002229
Germ Cell Tumor Molecular Heterogeneity Revealed through Analysis of Primary and Metastasis Pairs
Case Set
2020-08-26
phs002230
The UCSD / O'Connor "TSP" (Twin/Sibling/Pedigree) Resource in Hypertension
Family
2020-08-28
phs002231
Germ Cell and Associated Heme Malignancies Evolve from a Common Shared Precursor
Individual-Level Genomic Data
2020-08-31
phs002232
TOPDECC-Trans-omics for Precision Dentistry and Early Childhood Caries: Genome-Wide Genotyping (CIDR) and Microbiome in the ZOE 2.0 Study
Cross-Sectional
2020-09-01
phs002234
Deletion of FUNDC2 and CMC4 on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men
Case-Control
2020-09-02
phs002235
Global Microbiome Conservancy Sequence Data
Cross-Sectional
2020-09-02
phs002236
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetic and Phenotypic Determinants of Blood Pressure and Other Cardiovascular Risk Factors
Case-Control
2020-09-02
phs002237
Investigation of MMBIR DNA Repair in Normal and Cancer Human Cells
Tumor vs. Matched-Normal
2020-09-03
phs002238
Genomic Profiling of Relapsed and Refractory Childhood Cancers
Cohort
2020-09-03
phs002240
Characterization of Sex Differences in Human Placentas
Cohort
2020-09-04
phs002242
Center for Common Disease Genomics [CCDG] - Cardiovascular: SWISS-AF/SWISS-AF-PVI/BEAT-AF
Cohort
2020-09-08
phs002243
Center for Common Disease Genomics [CCDG] - Cardiovascular: PEGASUS-TIMI 54
Case-Control
2020-09-08
phs002244
A model for predicting response to PD-1 inhibitors in NSCLC
Cohort
2020-09-09
phs002245
Genetic Determinants of Susceptibility to Severe COVID-19 Infection
Cohort
2020-09-09
phs002249
HuBMAP: KULMAP - Human Kidney, Urinary Tract, and Lung Mapping Center
Epigenetics
2020-09-15
phs002250
CIDR: Discovery, Biology, and Risk of Inherited Variants in Glioma
Family
2020-09-17
phs002252
Cellular and Molecular Characterization of Renal Cell Carcinoma
Cohort
2020-09-18
phs002253
CCG Multicentric Italian Lung Detection (MILD)
Case Set
2020-09-18
phs002254
Cystic Fibrosis Nasal Epithelium Gene Expression by RNAseq
Cohort
2020-09-21
phs002255
Understanding the Biology of Language Impairment through Whole Genome Sequencing
Cohort
2020-09-22
phs002258
Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions
Clinical Diagnostic Testing
2020-09-28
phs002259
Human CD4 Memory T Cell Activation Time Course
eQTL
2020-09-29
phs002260
Characterization of Immune Evasion in Merkel Cell Carcinoma
Case Set
2023-01-05
phs002262
Characterization of High-Grade Serous Ovarian Cancer Subtypes via Single-Cell Profiling
Case Set
2022-11-10
phs002267
HuBMAP: A Spatially Resolved Molecular Atlas of Human Endothelium
Epigenetics
2020-10-07
phs002269
A New Pipeline to Predict and Confirm Tumor Neoantigens Predicts Better Response to Checkpoint Blockade
Case Set
2020-10-08
phs002270
Very Low Tumor Mutation Burden Identifies Inflamed Recurrent Glioblastomas Responsive to Cancer Immunotherapy
Exome Sequencing
2020-10-08
phs002272
HuBMAP: Single-Cell Data from Human Tissues
Collection
2020-10-08
phs002273
Analysis of Recurrently Protected Genomic Regions in Urine Cell-Free DNA
Methods Development
2020-10-12
phs002276
Gabriella Miller Kids First Pediatric Research Program in Pediatric T-Cell Acute Lymphoblastic Leukemia
Cohort
2021-09-24
phs002279
DNA and RNA sequencing of single human haploid germ cells
Case Set
2020-10-26
phs002280
Multimodal Analysis for Human Ex Vivo Studies Shows Extensive Molecular Changes from Delays in Blood Processing
Full Transcriptome Sequencing
2020-10-27
phs002282
Center for Common Disease Genomics (CCDG) - Cardiovascular: Harvard Gene-Diet Interaction in a Costa Rican Cohort
Whole Genome Sequencing
2020-10-28
phs002283
Selenium Chemoprevention: Benefits and Harms
Clinical Trial
2022-02-18
phs002284
Single Cell, Whole Genome Analysis of the Aging Human Cardiomyocytes
Single Cell Analysis
2020-10-31
phs002286
A Phase I/II Trial of T Cell Receptor Gene Therapy Targeting HPV-16 E7 for HPV-Associated Cancers
Clinical Trial
2020-11-02
phs002287
Evolution of Resistance in ER+ Breast Cancer
Case-Control
2020-11-12
phs002289
Yale SPORE in Skin Cancer Project 2
Single Cell Analysis
2020-11-17
phs002290
Tumor Fraction Guided Cell-Free DNA Profiling in Metastatic Cancer Patients
Sequencing
2020-11-18
phs002291
Whole Transcriptome Sequencing of Human Tumor Cells and Hematopoietic Stem and Progenitor Cells During Aging and Bone Marrow Disorders
Case Set
2020-11-18
phs002292
Functional Enhancer Elements Drive Subclass-Selective Expression From Mouse to Human Neocortex
Collection
2020-11-19
phs002294
Evolution of Core Archetypal Phenotypes in High-Grade Serous Ovarian Cancer (HGSOC)
Longitudinal
2020-11-20
phs002295
Cross-site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms of CIMAC-CIDC Network
Case Set
2020-11-20
phs002297
The Immune Microenvironment Shapes Transcriptional and Genetic Heterogeneity in Chronic Lymphocytic Leukemia
Cohort
2022-04-04
phs002298
Genome-wide association study of skin pigmentation in African Americans
Community
2020-12-01
phs002299
PETAL Network: Outcomes Related to COVID-19 Treated With Hydroxychloroquine Among Inpatients With Symptomatic Disease (ORCHID) Trial
Clinical Trial
2020-12-01
phs002300
Successful Clinical Response in Pneumonia Therapy (SCRIPT)
RNA Sequencing
2020-12-01
phs002301
Whole Genome Sequencing of Skull-Based Chordoma
Case Set
2020-12-04
phs002303
PEDS-PLAN - Pediatric Precision Laboratory Advanced Neuroblastoma Therapy
Case Set
2020-12-07
phs002304
Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Exome Sequencing
2020-12-07
phs002305
Washington University PDX Development and Trial Center
Tumor
2020-12-08
phs002307
CSER: South-Seq: DNA Sequencing for Newborn Nurseries in the South
Case Set
2020-12-08
phs002308
Characterizing Individual Cells Obtained from Bone Marrow Biopsies of MPN Patients
Clinical Cohort
2020-12-09
phs002309
Identification and Characterization of Skin-Resident Memory T cells in Patients with Melanoma-Associated Vitiligo
Cohort
2021-07-06
phs002310
International Collaboration of Incident HIV and HCV in Injecting Cohorts (InC3)
Longitudinal
2020-12-11
phs002311
GATA2 Deficiency
Case Set
2020-12-11
phs002313
Copy-Number Analysis of Understudied Black Women Ovarian Cancers
Case Set
2020-12-14
phs002315
Integrated Analysis of Multimodal Single-Cell Data
Case Set
2020-12-15
phs002316
Simultaneous Trimodal Single Cell Measurement of Transcripts, Epitopes, and Chromatin Accessibility Using TEA-Seq
Epigenetics
2020-12-15
phs002317
Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Genotype/Expression array
2020-12-16
phs002319
International Verapamil SR/Trandolapril [INVEST] Genes Study
Case-Control
2020-12-18
phs002321
Characterizing Advanced Breast Cancer Heterogeneity and Treatment Resistance through Serial Biopsies and Comprehensive Analytics
RNA Sequencing
2020-12-29
phs002322
Kids First: Genetics of Pediatric Germ Cell Tumors
Parent-Offspring Trios
2020-12-29
phs002323
Defining and Overcoming Intrinsic T Cell Dysfunction to Enable Pediatric Immunotherapy
Case Set
2022-05-23
phs002324
CSER: Genomic Sequencing to Aid Diagnosis in Pediatric and Prenatal Practice: Examining Clinical Utility, Ethical Implications, Payer Coverage, and Data Integration in a Diverse Population
Parent-Offspring Trios
2023-02-22
phs002325
Center for Common Disease Genomics (CCDG) - Cardiovascular: BioImage Cohort
Case-Control
2021-01-07
phs002327
Therapeutic Targeting of ATR Yields Durable Regressions in High Replication Stress Tumors
Clinical Trial
2021-01-11
phs002328
International Genetics of Parkinson Disease Progression (IGPP) Consortium: EPIPARK and HBS2 Cohorts
Longitudinal Cohort
2021-01-12
phs002330
Kids First and INCLUDE: Down Syndrome, Heart Defects, and Acute Lymphoblastic Leukemia
Cohort
2021-01-19
phs002331
Prevention of Viral Hepatitis and HIV in Drug Users - A Hepatitis B Model for HIV and an HB Vaccine Model for HIV Vaccine Trials in Drug Users (DASH)
Clinical Trial
2021-01-21
phs002333
Massively Parallel Single-Cell RNA-Sequencing of Chronic Rhinosinusitis Nasal and Sinus Tissue
Clinical Cohort
2021-01-26
phs002334
Genetic Determinants of EGFR-Driven Lung Cancer Growth and Therapeutic Response In Vivo
Cohort
2021-01-28
phs002335
Dana-Farber Cancer Institute (DFCI) Wu Lab/Avicenne CLL RNA-Seq Study
Cohort
2021-01-28
phs002336
NIDDK International IBD Genetics Consortium Repository Global Screening Array
Case-Control
2021-01-28
phs002337
CSER: Incorporating Genomics into the Clinical Care of Diverse NYC Children (NYCKidSeq)
Clinical Diagnostic Testing
2023-01-11
phs002340
A Multi-Omic Single-Cell Atlas of Human Gynecological Malignancies
Case Set
2021-02-03
phs002341
RNA Expression in Diverse Donor Derived Dermal Fibroblasts Correlates with Reprogramming to Pluripotency
Cohort
2021-02-04
phs002342
Optimized Polyepitope Neoantigen DNA Vaccines Elicit Neoantigen-Specific Immune Responses in Preclinical Models and in Clinical Translation
Individual-Level Genomic Data
2021-02-05
phs002344
Study of Tumor Recurrence Related to the Expression of the PAX3-FOXO1 Oncogenic Transcription Factor in Fusion-Positive Rhabdomyosarcoma
Case Set
2021-02-05
phs002346
Characterization of Immune-Related Gene Expression in Lung Cancer
Case Set
2021-02-09
phs002347
PDAC Prognosis Biomarkers in Genomic and Transcriptomic Molecular Data
Copy Number Variation (CNV)
2021-02-09
phs002348
Multicenter Study of Hydroxyurea (MSH)
Double-Blind
2021-02-10
phs002357
Lineage Plasticity and Immune Cell Heterogeneity Are Coordinately Dysregulated Through Changes in FOXA1 Expression in Bladder Cancers with Squamous Differentiation
Exome Sequencing
2021-02-17
phs002361
Genomics and Epigenomics of the Elderly Response to Pneumococcal Vaccines
Clinical Cohort
2021-02-22
phs002362
Cooperative Study of Sickle Cell Disease (CSSCD)
Case-Control
2021-02-23
phs002363
PETAL Repository of Electronic Data COVID-19 Observational Study (RED CORAL)
Case-Cohort
2021-02-25
phs002364
Oral Mucosa Transcriptomic Data from Three HIV+cART Patients
Case Set
2021-02-25
phs002365
Derivation and Investigation of The First Human Cell-Based Model of Beckwith-Wiedemann Syndrome
Cohort
2021-02-26
phs002367
Longitudinal Study of Vaginal Flora
Longitudinal Cohort
2021-03-02
phs002368
CaBagE: a Cas9-Based Background Elimination Strategy for Targeted, Long-Read DNA Sequencing
Case Set
2021-03-02
phs002371
Human Tumor Atlas Network (HTAN)
Clinical Diagnostic Testing
2023-03-16
phs002372
Novel Approach to High-Throughput Identification and Characterization of Neoantigens
Methods Development
2021-03-08
phs002373
Avelumab or M7824 for People with Recurrent Respiratory Papillomatosis
Case Set
2021-03-09
phs002377
A Phase I/IB Study of Ipilimumab or Nivolumab in Patients With Relapsed Hematologic Malignancies After Allogeneic Hematopoietic Cell Transplantation
Clinical Trial
2021-03-10
phs002380
Characterizing TP53 and PPM1D Mutations as Resistance Drivers to Radiation Therapy in Diffuse Intrinsic Pontine Gliomas
Case Set
2021-03-16
phs002383
Treatment of Pulmonary Hypertension and Sickle Cell Disease with Sildenafil Therapy (Walk-PHaSST)
Clinical Trial
2021-03-18
phs002385
Hematopoietic Cell Transplant for Sickle Cell Disease (HCT for SCD)
Clinical Cohort
2021-03-19
phs002386
Optimizing Primary Stroke Prevention in Children with Sickle Cell Anemia (STOP II)
Clinical Trial
2021-03-19
phs002387
Ghana Breast Health Study
Case-Control
2021-03-22
phs002388
Genomic and Transcriptomic Markers Associated with Response to Immune Checkpoint Blockade
Clinical Cohort
2021-03-22
phs002389
MicroRNAs, Hypertension and End Organ Damage in Humans
Case-Control
2021-06-09
phs002391
De Novo Mutation Rates at the Single-Mutation Resolution in the Human Genome
Sequencing
2021-03-24
phs002392
Transcriptome of 2-Hydroxypropyl-Beta-Cyclodextrin Treatment in Niemann-Pick Disease Type C1
Clinical Cohort
2021-03-25
phs002393
Precision Medicine for ABCA4 Disease: Modifier Alleles
Case Set
2022-01-26
phs002394
Chromatin Accessibility Landscape of Human Pancreatic Ductal Adenocarcinoma (PDAC)
Clinical Cohort
2021-03-26
phs002395
Mitochondrial Abnormalities in Schizophrenia and Bipolar Disorder
Case-Control
2021-04-01
phs002396
Integrated Metabolic Profiling and Gene Expression Analysis Reveals Therapeutic Modalities in Breast Cancer
Tumor vs. Matched-Normal
2021-04-06
phs002398
Genomics of Prostate Cancer
Case Set
2021-04-10
phs002400
The Role of Myeloid Cells in Parkinson's Disease
Case-Control
2021-04-14
phs002401
High Glucose Macrophage Exosomes Enhance Atherosclerosis by Driving Cellular Proliferation and Hematopoiesis
Cohort
2021-04-14
phs002405
Gene Variants in Pheochromocytoma and Paraganglioma
Case Set
2021-04-19
phs002406
The Northern Manhattan Family Study - a Sub-Study of the Epidemiologic Study of Stroke Outcome in 3 Ethnic Groups: The Northern Manhattan Study
Cohort
2021-04-19
phs002407
A Single Cell Atlas of MMRd and MMRp Colorectal Cancer
Case Set
2021-04-22
phs002408
The Role of CTCF in the Organization of the Centromeric 11p15 Imprinted Domain Interactome
Case-Control
2021-04-22
phs002410
FHIR Test Study BETA
Longitudinal Cohort
2021-04-25
phs002411
Genome Instability in Mammary Cells of Pathogenic BRCA1/2 Mutation Carriers
Cross-Sectional
2021-04-26
phs002414
Human Companion Data for 'A Transcriptomic Atlas of Mouse Cerebellar Cortex Reveals Novel Cell Types'
Control Set
2021-04-29
phs002415
Hydroxyurea to Prevent Organ Damage in Children with Sickle Cell Anemia (BABY HUG) Phase III Clinical Trial and Follow-Up Observational Studies I and II
Clinical Cohort
2021-04-30
phs002416
Characterization of CNS Metastases
Case Set
2022-02-16
phs002417
Low Density Genotyping from the Fragile Families and Child Wellbeing Study
Longitudinal
2021-05-05
phs002419
Integrative Molecular Characterization of Breast Cancer
Case Set
2021-05-06
phs002421
Transcriptomic Profiling of Patient Derived Alternative Lengthening of Telomeres (ALT) and Non-MYCN-Amplified Neuroblastoma Cell Lines
Cohort
2021-05-07
phs002422
Experimental PfSPZ Vaccine in Adults Without Malaria
Interventional
2021-05-11
phs002423
Study of Controlled Human Malaria Infections to Evaluate Protection After Intravenous or Intramuscular Administration of PfSPZ Vaccine in Malaria-Naive Adults
Interventional
2021-05-11
phs002424
Epigenetic Moderators of Naltrexone Efficacy for Alcohol Use Disorder
Clinical Trial
2021-05-11
phs002428
Tandem DNA Repeats Activate hTERT Gene Transcription
Case-Control
2021-05-14
phs002429
UNC Tumor Donation Program Set 2021
Case Set
2021-05-14
phs002430
Childhood Cancer Data Initiative (CCDI): Genomic Analysis in Pediatric Malignancies
Clinical Genetic Testing
2021-05-14
phs002432
Wistar PDX Development and Trial Center
Case Set
2021-05-18
phs002433
Nasopharyngeal RNASeq Comparing SARS-CoV-2+ Patients and SARS-CoV-2 Negative Control Subjects
Collection
2021-05-18
phs002435
Development and Validation of Patient-Derived Xenografts from Fibrolamellar Carcinoma Human Tissue
Case Set
2021-05-19
phs002436
Transcriptome and Epigenome of TIL Infusion for Cancer Immunotherapy
Case Set
2021-05-20
phs002437
Metformin for Oral Cancer Prevention
Case Set
2021-05-21
phs002439
Development and Validation of Organoids from Fibrolamellar Carcinoma Human Cells
Case Set
2021-05-22
phs002440
Parallel CRISPR Editing of Familial ALS Mutations Into a Healthy Control iPSC Line
Exome Sequencing
2021-05-24
phs002441
High-Throughput and High-Dimensional Single Cell Analysis of Antigen-Specific CD8+ T Cells
Cohort
2021-05-25
phs002442
Host Response to Respiratory Infections
Collection
2021-05-25
phs002443
Molecular Signatures of DCIS to Invasive Progression for Basal-Like Breast Cancers: An Integrated Mouse Model and Human Tumor Study
Cohort
2021-05-26
phs002444
Germline Genetic Variants in Cancer-Susceptibility Genes in Patients with Osteosarcoma
Case Set
2021-05-27
phs002445
Resistance to Latent Mycobacterium tuberculosis Infection in Uganda: Immunologic Profiling
Case-Control
2023-03-13
phs002446
Single Cell Omics Resolves Transcriptional Alterations in Sjogren's Syndrome
Cross-Sectional
2021-05-28
phs002447
Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY)
Clinical Trial
2021-06-01
phs002448
Inhibition of CDK4/6 Promotes CD8 T Cell Memory
Clinical Cohort
2021-06-01
phs002449
Tissue and Fluid Analysis in Ocular Inflammatory Disease
Cross-Sectional
2021-06-02
phs002450
Genomic Basis of Phenotypic Variability of Complex Disorders
Copy Number Variation (CNV)
2021-06-02
phs002453
Million Veteran Program (MVP) Summary Results from Non-Sensitive Omics Studies
Clinical Cohort
2021-06-03
phs002455
Dissecting Autoimmune Cellular and Molecular Networks in Vitiligo
Case-Control
2021-06-04
phs002456
Integrated Genomic Analyses of Cutaneous T Cell Lymphomas Reveal the Molecular Bases for Disease Heterogeneity
Case Set
2021-06-07
phs002457
Comprehensive Analysis of the Immunogenomics of Triple Negative Breast Cancer Brain Metastases from LCCC1419
Tumor vs. Matched-Normal
2021-06-07
phs002458
Evolution of Chronic Lymphocytic Leukemia to Richter's Syndrome (RS)
Longitudinal
2021-06-08
phs002460
Health Professionals Follow-Up Study
Longitudinal
2021-06-09
phs002461
Single-Cell Analysis of Human Adipogenesis
Full Transcriptome Sequencing
2022-07-07
phs002462
Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis
Case Set
2021-06-09
phs002463
Natural Genetic Variation in the Human Genome
Collection
2021-06-10
phs002464
Leveraging Extended Families for Cardiovascular Disease Genomic Discovery
Exome Sequencing
2021-06-11
phs002465
The Human Pancreas Analysis Program (HPAP)
Case-Control
2021-06-11
phs002467
Multimodal Profiling of 500,000 Memory T Cells from a Tuberculosis Cohort Identifies Cell State Associations with Demographics, Environment, and Disease
Case-Control
2021-06-16
phs002468
Type 1 Diabetes Genetics Consortium (T1DGC): Multi-Ethnic ImmunoChip Study
Case-Control
2021-06-17
phs002470
A Polygenic Score for Acute Vaso-Occlusive Pain in Pediatric Sickle Cell Disease
Clinical Cohort
2021-06-21
phs002471
Base Editing Reduces Misfolded Protein Accumulation and Toxicity in Alpha-1 Antitrypsin Deficient Patient iPSC-Hepatocytes
Collection
2021-06-22
phs002472
Airway Epithelial Cell Culture RNA Expression
Cohort
2021-06-22
phs002476
Immune Profiling in Patients with High-Risk Smoldering Myeloma
Case-Control
2023-04-19
phs002478
iRHOM2 Deficiency Causes Environmentally Directed Immunodysregulatory Disease
Case Set
2021-06-24
phs002479
HCI-PDX Trial Center for Breast Cancer Therapy
Case Set
2021-06-24
phs002480
Genomics of Glomerular Disorders
Case Set
2022-01-31
phs002481
Gene Expression Study of Individuals with Sex Chromosome Aneuploidies
Case-Control
2022-02-24
phs002482
Combined Targeting of CDK4/6 and HER2 Signaling in Orthotopic Patient-Derived Xenografts of HER2-Positive Breast Cancer Brain Metastases
Exome Sequencing
2021-06-28
phs002484
Bulk RNA Sequencing of 86 Human Donor Lungs
RNA Sequencing
2021-07-01
phs002486
Nivolumab and Tumor Infiltrating Lymphocytes (TIL) in Advanced Non-Small Cell Lung Cancer
Clinical Trial
2021-07-02
phs002487
Epigenomes and Transcriptomes of Brain Samples of Schizophrenics and Controls
Case-Control
2021-07-02
phs002489
Developmental Dynamics of Translation in the Human Brain
Collection
2021-07-05
phs002492
Study of Leukemia Stem Cells in B-ALL
Case Set
2021-07-08
phs002493
Genetic Effects on Gene Expression and Splicing during Human Neurogenesis
eQTL
2021-07-08
phs002495
Clinical and Genetic Analysis of Costa Rican Patients with Parkinson's Disease
Case-Control
2021-07-12
phs002496
Germline Whole-Exome Sequencing of Lung Cancer in EAGLE
Case-Control
2021-07-13
phs002498
Integrative Genomic and Transcriptomic Analyses of Refractory Multiple Myeloma
Case Set
2021-07-13
phs002499
Primary Cytotoxic T Cell Lymphomas Harbor Recurrent Targetable Alterations in the JAK-STAT Pathway
Case Set
2021-07-14
phs002502
Center for Common Disease Genomics [CCDG] Neuropsychiatric: Autism Spectrum Disorder (ASD) – Whole Exomes
Parent-Offspring
2023-04-11
phs002504
UCSF Database for the Advancement of JMML - Integration of Metadata with "Omic" Data
Clinical Cohort
2021-07-20
phs002505
CPTAC: Molecular Dissection of Chemotherapy Response in Triple Negative Breast Cancer
Case Set
2021-07-21
phs002506
Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome Phenotypes
Case Set
2021-07-21
phs002507
Developmental Maturation of Hematopoietic Stem and Progenitor Cells Mediated by Lin28b/Let-7/Cbx2
Stem Cell Lines
2021-07-23
phs002508
Human Vaccines Project: scRNAseq Characterization of HepB Vaccine Response
Single Cell Analysis
2021-07-26
phs002509
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD)
Family
2021-07-26
phs002510
Mechanisms of Restoring T Cell Immunity after Cure of Chronic Viral Infection
Epigenetics
2021-07-26
phs002511
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: SPARK Simons Foundation Powering Autism Research for Knowledge
Family
2021-07-26
phs002512
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Simons Searchlight
Family
2021-07-26
phs002513
Study of Environment, Lifestyle and Fibroids SNP Data
Longitudinal Cohort
2021-07-27
phs002515
Mutational Landscape of MCPyV-Positive and MCPyV-Negative Merkel Cell Carcinomas
Case Set
2021-07-27
phs002516
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: IBM Covid19 Contact Tracing and Data Exchange Tools
Longitudinal
2021-07-27
phs002517
Childhood Cancer Data Initiative (CCDI): Molecular Characterization across Pediatric Brain Tumors and Other Solid and Hematologic Malignancies for Research, Diagnostic, and Precision Medicine
Clinical Cohort
2021-07-27
phs002518
Childhood Cancer Data Initiative (CCDI): OncoKids - NGS Panel for Pediatric Malignancies
Case Set
2021-07-27
phs002519
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Covidseeker and COVID-19 Citizen Science: Leveraging Citizen Science and Real-Time Geospatial Temporal Mobile Data for Digital Contact Tracing and SARS-CoV-2 Hotspotting
Case Set
2021-07-27
phs002528
Neuropsychiatric Genetics of African Populations - Psychosis (NeuroGAP-Psychosis)
Case-Control
2021-07-28
phs002529
Childhood Cancer Data Initiative (CCDI): Comprehensive Genomic Sequencing of Pediatric Cancer Cases (CMRI/KUCC)
Case Set
2021-07-28
phs002533
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Digital Health Solutions for COVID-19: COVID Community Action and Research Engagement (COVID-CARE)
Cohort
2021-08-02
phs002534
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: Team SAE
Cohort
2021-08-02
phs002537
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): COVID-19 Experience Study (C19EX) Survey
Longitudinal
2021-08-02
phs002538
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): ILI Labels and Longitudinal Novel Engagement with Symptom Surveillance (ILLNESS) Study
Observational
2021-08-02
phs002539
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Large Scale Flu Surveillance Study (LSFS)
Longitudinal
2021-08-02
phs002540
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: SAFER-COVID - Integration of Testing and Digital Health
Longitudinal
2021-08-03
phs002541
Integrated Genomic and Transcriptomic Analysis of Small Cell Lung Cancer Reveals Inter- and Intratumoral Heterogeneity and a Novel Chemotherapy-Refractory Subtype
Cross-Sectional
2021-08-04
phs002545
Nivolumab and Ipilimumab and Radiation Therapy in Microsatellite Stable (MSS) and Microsatellite Instable (MSI) High Colorectal and Pancreatic Cancer
Case Set
2021-08-05
phs002548
Transcriptome of Chronic Pain and Disease
Case-Control
2021-08-09
phs002552
Genomic Analysis of Low Grade B-Cell Lymphoma
Case Set
2021-08-10
phs002554
Gene Expression and Epigenetic Analyses of Human Myocytes From Different Muscles
Case-Control
2022-01-14
phs002556
Genomic Features of Lung Adenocarcinoma from Individuals with <= 10 Pack-Year Smoking History
Case Set
2021-08-13
phs002557
Homozygous Duplication Identified by Whole Genome Sequencing Causes LRBA Deficiency
Case Set
2021-08-13
phs002562
Utlizing the RA signature to predict response to TNFi
Full Transcriptome Sequencing
2021-08-17
phs002564
Transcriptional Profiling of Macrophages In Situ in Metastatic Melanoma Reveals Localization-Dependent Phenotypes and Function
Metastasis
2021-08-18
phs002566
Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer Risk
Case-Control
2021-08-21
phs002571
Exome Sequencing for Head and Neck Cancer Susceptibility
Sequencing
2021-08-24
phs002579
Immune Response to Life-Threatening Respiratory Infections in Children and Young Adults
Cross-Sectional
2021-08-27
phs002587
Preclinical Modeling of Leiomyosarcoma Identifies Susceptibility to Transcriptional CDK Inhibitors through Antagonism of E2F-Driven Oncogenic Gene Expression
RNA Sequencing
2021-09-02
phs002589
Kids First: Congenital Heart Defects and Laterality Birth Defects
Cohort
2021-09-03
phs002590
Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects
Parent-Offspring Trios
2021-09-03
phs002591
Kids First: Whole Genome Sequencing in Structural Defects of the Neural Tube
Parent-Offspring Trios
2021-09-03
phs002592
Kids First: Genomic Etiologies of CHARGE Syndrome, Related Conditions and Structural Anomalies
Cohort
2021-09-03
phs002594
Kids First: Genetic Basis of Fetal Alcohol Spectrum Disorders
Cohort
2021-09-03
phs002595
Kids First: Genomics of Orofacial Clefts in the Philippines
Cohort
2021-09-03
phs002597
DNA Replication Timing Alterations in Genetic Diseases
Aggregate Genomic Data
2022-06-07
phs002598
Inherited Defect in ST6GalNAc1 Reveals Roles of Sialylation in Intestinal Homeostasis
Exome Sequencing
2021-09-07
phs002599
NCI CCSG CCDI Supplement Additional Genomic Submission
Case Set
2021-09-07
phs002607
Modeling Malignant Progression in Glioma
Case Set
2021-09-09
phs002610
Maintenance of Genome Sequence Integrity in Long- and Short-lived Rodent Species
Single Cell Analysis
2023-02-02
phs002612
Immunogenomics of Malignant Brain Tumors
Exome Sequencing
2021-09-16
phs002613
Characterizing Disease-Causing Variants Using Personal Genomes with Large Recurrent Deletions
Clinical Genetic Testing
2021-09-16
phs002614
Multi-Omic Investigation of Beckwith-Wiedemann Syndrome Hepatoblastoma
Epigenetics
2021-09-20
phs002615
Somatic Mutations in Epilepsy: Whole Genome Sequence Analysis of Single Neurons
Case Set
2021-09-20
phs002620
Feasibility and Clinical Utility of Whole Genome Profiling in Pediatric and Young Adult Cancers
Case Set
2021-09-24
phs002621
CIDR: NINDS High Throughput Genotyping Resource Access for Structural Hindbrain Disorders
Case-Control
2021-09-24
phs002622
Aurora US Metastatic Breast Cancer Retrospective Project
Case Set
2021-09-28
phs002623
Whole Genome Sequencing of Bilateral Cleft Lip and Palate Families from Africa: CIDR
Parent-Offspring
2021-09-28
phs002624
Clonal Lineage Tracing of Primary Human Cortical Progenitors, Cell Type Profiles in the Brain Vasculature and Genotyping Data for 22q11DS and Control iPS Lines
Cohort
2021-12-29
phs002625
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Exome Sequencing
2021-10-04
phs002627
Kids First: The Genomic Basis of Structural Birth Defects Associated with Chromosome 18 Copy Number Changes
Cohort
2021-10-04
phs002628
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: Clear2Go - A Digital Identity Wallet for Health Status
Clinical Trial
2021-10-04
phs002632
Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82
Case Set
2021-10-05
phs002635
Myelofibrosis Etiology and Transplant Outcomes
Case Set
2021-10-06
phs002637
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Case-Control
2021-10-06
phs002639
Genomic Analysis of Metastatic Brain Cancer
RNA Sequencing
2021-10-13
phs002641
Precision Medicine for Dilated Cardiomyopathy in European and African Ancestry
Case Set
2021-10-15
phs002652
Identification of Somatic Changes in Tumors from Fanconi Anemia Patients
Copy Number Variation (CNV)
2021-10-18
phs002653
Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas
Aggregate Genomic Data
2021-10-19
phs002654
Genetic Study of Northern Kenya Pastoral Populations
Cohort
2021-10-19
phs002659
Genomics from LCCC1525: A Priming Dose of Cyclophosphamide Prior to Pembrolizumab to Treat mTNBC
Case Set
2021-10-21
phs002678
Microbiome-Host Interactions in Oral Squamous Cell Carcinoma: a Metatranscriptomic Exploratory Study
RNA Sequencing
2021-10-27
phs002681
Natural Killer Cell Therapies for Hematologic Malignancies
Clinical Trial
2021-10-29
phs002683
Combined Tumor and Immune Signals From Genomes or Transcriptomes Predict Outcomes of Checkpoint Inhibition in Melanoma
Case Set
2021-10-29
phs002684
Single Suture Craniosynostosis: Gene and Pathway Discovery
Case Set
2021-10-29
phs002686
Immunophenotyping in a COVID-19 Cohort (IMPACC) Transcriptomics and Genotyping Assays
Clinical Cohort
2021-11-01
phs002687
RNA-Seq of Whole Blood from Pediatric Sickle Cell Anemia (SCA) Patients
Case-Control
2021-11-04
phs002688
CIDR Estrogen Receptor Negative Breast Cancer in African American Women: DNA Methylation, Reproductive Events, and Mammary Epithelial Cell Populations
Case Set
2021-11-05
phs002691
The MD Anderson Colorectal Cancer Case Control Study
Case-Control
2021-11-09
phs002692
Pulmonary Fibrosis and Telomerase Dysfunction
Case Set
2021-11-10
phs002694
COVID-19 ACTIV-4 ACUTE: A Multicenter, Adaptive, Randomized Controlled Platform Trial of the Safety and Efficacy of Antithrombotic Strategies in Hospitalized Adults with COVID-19 (ACTIV4A)
Clinical Trial
2023-02-21
phs002695
Development of Computational Approaches for Cell Hashing in scRNA-Seq
Sequencing
2021-11-17
phs002697
A Multimodal Atlas of Human Brain Cell Types 2021 Data
Transcriptome Sequencing
2021-11-17
phs002698
Identification of Structural Variants Relevant to Autism by Pacific Biosciences HiFi Whole-Genome Sequencing
Affected Sib Pairs
2021-11-18
phs002701
The Role of ZEB2 during Human Neural Crest Cell Formation
RNA Sequencing
2021-11-18
phs002703
SEARCH for Diabetes in Youth Study - Genetic Risk Score
Case-Cohort
2021-11-19
phs002705
Single Cell Analysis Reveals Immune Dysfunction from the Earliest Stages of CLL that can be Reversed by Ibrutinib
Observational
2021-11-22
phs002706
Transformation of Dysplasia in Barrett's Esophagus
Case Set
2021-11-22
phs002710
COVID-19 Outpatient Thrombosis Prevention Trial (ACTIV-4B)
Clinical Trial
2021-11-23
phs002714
The National Myelodysplastic Syndromes (MDS) Study
Clinical Trial
2021-11-23
phs002715
National Sleep Research Resource (NSRR): Cleveland Family Study (CFS)
Longitudinal Cohort
2021-11-24
phs002716
Genetics of Hypertension Associated Treatment (GenHAT) Study, Genomic Background of Blood Pressure Response to Treatment in African Americans
Clinical Trial
2021-11-30
phs002717
Study of Cutaneous Biology of Cutaneous T Cell Lymphoma
Case-Cohort
2021-12-02
phs002718
Genetics of Prostate Cancer in Africa
Case-Control
2021-12-02
phs002719
Reasons for Geographic and Racial Differences in Stroke Cardiorenal GWAS
GWAS
2021-12-03
phs002723
Discovery and Characterization of Genetic Risk Loci in Sjogren's Syndrome
Case-Control
2021-12-06
phs002724
(Epi)genetic Risk Architectures of Opioid-Dependent Brain
Case-Control
2021-12-07
phs002725
Novel Gene-Environment Regulatory Circuit in Chamber-Specific Growth of Perinatal Heart
Exome Sequencing
2021-12-08
phs002726
Center for Common Disease Genomics [CCDG] - Cardiovascular: Cardiology Biobanking for Biomarker Discovery
Case Set
2021-12-08
phs002728
RNA-Seq of PBMC's from rUTI Patients and Healthy Controls
Cohort
2021-12-09
phs002731
Multi-Omic Analysis of Von Willebrand Factor Regulation in Endothelial Colony Forming Cells
Case-Control
2021-12-13
phs002733
Colon Cancer Family Registry (Colon CFR)
Case-Control
2021-12-14
phs002734
Rapid Idiosyncratic Mechanisms of Clinical Resistance to KRAS G12C Inhibition
Case Set
2021-12-15
phs002735
Tumor Infiltrating Lymphocytes (TIL) Recognize Unique Somatic Mutations and Mediate Objective Clinical Responses in Metastatic Breast Cancer
Cohort
2021-12-16
phs002746
Resistance to Latent Mycobacterium tuberculosis Infection in South Africa: Immunologic Profiling
Case-Control
2021-12-17
phs002748
Transcriptome and TCR Sequencing of T Cells from Metastectomies
Case Set
2021-12-20
phs002752
Clinical Trial of COVID-19 Convalescent Plasma in Outpatients (C3PO)
Clinical Trial
2021-12-23
phs002753
Ameloblastoma Cell Line Resource
Exome Sequencing
2021-12-23
phs002754
PROGRESS/ELEMENT DNA Methylation Study
Cohort
2021-12-27
phs002756
Characterizing the Role of the Immune Microenvironment in Multiple Myeloma Progression at a Single Cell Level
Case Set
2021-12-28
phs002758
Single-Cell Analysis of Somatic Mutations in Human Bronchial Epithelial Cells in Relation to Aging and Smoking
Cross-Sectional
2022-01-04
phs002762
Functional Multiomics of Cellular Therapy and Immune Checkpoint Blockade Therapy for Solid Tumors
Longitudinal
2022-01-11
phs002764
Dissecting Cell Composition and Drug Sensitivity in Human Adenoid Cystic Carcinomas (ACCs)
Exome Sequencing
2022-01-12
phs002765
Transcriptomic Profiles of Neoantigen-Reactive T Cells in Human Gastrointestinal Cancers
Case Set
2022-01-13
phs002766
Generation of a Cellular Atlas of Human Adipose Tissue
Collection
2022-01-13
phs002767
Epidemiologic Architecture for Genes Linked to Environment (EAGLE) MetaboChip Study
Electronic Medical Records
2022-01-15
phs002769
Multi-Omic Investigation of Beckwith-Wiedemann Syndrome Wilms Tumor
Cohort
2022-01-18
phs002771
SLAMF7 Regulates Synovial Macrophages in Rheumatoid Arthritis
Full Transcriptome Sequencing
2022-01-18
phs002774
Center for Common Disease Genomics [CCDG] - Cardiovascular: ENGAGE Atrial Fibrillation-TIMI 48
Case Set
2022-01-19
phs002780
IFN-γ and TNF-α drive a CXCL10+ CCL2+ Macrophage Phenotype Expanded in Severe COVID-19 Lungs and Inflammatory Diseases with Tissue Inflammation
RNA Sequencing
2022-01-25
phs002783
Pan Cancer Investigation of Human Leukocyte Antigen Loss of Heterozygosity
Case Set
2022-01-25
phs002787
Personalized Breast Cancer Vaccines Based on Genome Sequencing
Exome Sequencing
2022-01-27
phs002790
Childhood Cancer Data Initiative (CCDI): Molecular Characterization Initiative
Aggregate Genomic Data
2023-02-24
phs002792
Characterization of Neoantigen-reactive T cells by Single-Cell Analysis
Case Set
2022-02-01
phs002793
Study of Lyme Immunology and Clinical Events (SLICE)
Case-Cohort
2022-09-14
phs002802
Phase IB/II Study of Bazedoxifene in Combination with Palbociclib in Patients with Endocrine Resistant Hormone Receptor-Positive Breast Cancer
Prospective
2022-02-10
phs002803
A Phase II Clinical Trial of the PARP Inhibitor Talazoparib in BRCA1 and BRCA2 Wild-Type Patients
Clinical Trial
2022-02-10
phs002804
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Case-Control
2022-02-10
phs002808
Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be Heart Health Study (nuMoM2b Heart Health Study)
Longitudinal Cohort
2022-02-10
phs002809
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Case-Control
2022-02-10
phs002810
Genetic Analysis of Latin American Cervical Cancer
Case Set
2022-02-11
phs002811
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Genetics of Atrial Fibrillation
Case Set
2022-02-14
phs002812
Multiplexed scRNA-Seq Reveals Cellular and Genetic Correlates of SLE
Case-Control
2022-02-14
phs002814
Esophageal Squamous Cell Carcinoma Precursor Study
Case Set
2022-02-15
phs002815
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts, Sub-types, and Subclinical Phenotypes - CIDR
Case-Control
2022-02-16
phs002816
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Exome Sequencing
2022-02-16
phs002817
Mutations in GNAI2 Cause Developmental and Immune Dysregulation
Case Set
2022-02-16
phs002818
Intercepting Progression from Pre-Invasive to Invasive Lung Adenocarcinoma
Exome Sequencing
2022-02-17
phs002819
Single-Nuclei Paired Multiomic Analysis of Young, Aged, and Parkinson's Disease Human Midbrain Reveals Age-Associated Glial Changes and Their Contribution to Parkinson's Disease
Case-Control
2022-02-17
phs002820
Cancer Risk Estimates Related to Susceptibility Genes (CARRIERS)
Case-Control
2022-02-17
phs002822
SU2C-MARK Lung Cancer Consortium - Checkpoint Blockade Response Project
Clinical Cohort
2022-02-18
phs002826
Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy
Interventional
2022-02-23
phs002833
A Phase 2 Study of Lamivudine in Patients with p53 Mutant Metastatic Colorectal Cancer
Clinical Trial
2022-02-28
phs002834
Clinical and Molecular Features of Acquired Resistance to Immunotherapy in Non-Small Cell Lung Cancer
Case Set
2022-03-03
phs002835
Breast Cancer Family Registry
Cohort
2022-03-03
phs002840
The Transcriptomic Landscape of Oncogenic PI3K Reveals Key Functions in Splicing and Gene Expression Regulation
Clinical Trial
2022-03-09
phs002842
Gene Expression in an African American Schizophrenia Dataset
RNA Sequencing
2022-03-10
phs002845
Expression of Activation Induced Cytidine Deaminase and Risk of Transformation in Follicular Lymphoma
Clinical Cohort
2022-03-13
phs002846
Pharmacogenomics of Mercaptopurine Intolerance in Children with Acute Lymphoblastic Leukemia (AALL03N1)
Clinical Cohort
2022-03-15
phs002847
Circulating Tumor DNA as a Biomarker in Patients with Stage III and IV Wilms Tumor: Analysis from a Children's Oncology Group Trial, AREN0533
Case Set
2022-03-15
phs002849
A Sequential Window of Opportunity Trial of Anti-PD-L1/TGF-β trap (M7824) Alone and in Combination with TriAd Vaccine and N-803 for Resectable Head and Neck Squamous Cell Carcinoma not Associated with Human Papillomavirus Infection
Prospective
2022-03-21
phs002852
A Pilot Study of NKTR-214 and Nivolumab in Selected Patients with Locally Advanced/Metastatic Sarcoma
Clinical Trial
2022-03-23
phs002856
Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands
Cohort
2022-03-28
phs002857
MSK SPECTRUM - SPatiotemporal Evolution of Cancer Traced Using Multimodalities
Case Set
2022-03-29
phs002858
The Mood and Methylation Study (MMS)
Epigenetics
2022-03-30
phs002859
RB1 Loss Triggers Dependence on ESRRG in Retinoblastoma
Exome Sequencing
2022-03-30
phs002861
Genomic Data Archive From the Network for Pancreatic Organ Donors With Diabetes
Case-Control
2022-03-31
phs002862
Improved T Cell Immunity Following Neoadjuvant Chemotherapy in Ovarian Cancer
Longitudinal
2022-04-01
phs002863
Genome-Wide Association Study of Heparin-Induced Thrombocytopenia
GWAS
2022-04-04
phs002864
Genomic Analyses in Neoadjuvant Immunotherapy-Treated Head and Neck Cancers
Clinical Cohort
2022-04-04
phs002865
Accurate Genome-Wide Germline DNA Profiling from Decade-Old Archival Tissue Specimens
Sequencing
2022-04-04
phs002866
Circulating Tumor DNA in Intermediate Risk Rhabdomyosarcoma
Case Set
2022-04-05
phs002867
Blood Somatic Mutations in TCGA Donors Suffering from Solid Tumors
Case Set
2022-04-05
phs002876
CTN - 0051: Extended-Release Naltrexone vs. Buprenorphine for Opioid Treatment (X:BOT)
Multicenter
2022-04-07
phs002877
Mapping the Evolution of T Cell States During Response and Resistance to Adoptive Cellular Therapy
Longitudinal
2022-04-08
phs002879
Vulnerabilities of Midbrain Dopaminergic Neurons to Parkinson's Disease Revealed by Single-Cell Genomics
Cross-Sectional
2022-04-12
phs002881
The Pathogenesis and Genetics of Disseminated Coccidioidomycosis
Cohort
2022-04-14
phs002902
Ribosomal Depleted Total RNA-Seq of PBMCs and Skin from Controls and Systemic Sclerosis Patients
Case-Control
2022-05-04
phs002903
The Role of CDX2 in Controlling ABCB1 Expression and Chemosensitivity in Human Colon Cancer
Marker Discovery
2022-05-04
phs002910
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Genetic Epidemiology of COPD Study (COPDGene)
Longitudinal Cohort
2022-05-06
phs002911
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Framingham Heart Study (FHS)
Longitudinal Cohort
2022-05-06
phs002913
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Severe Asthma Research Program (SARP)
Longitudinal Cohort
2022-05-09
phs002914
Ultrasensitive Profiling of UV Mutations in Facial Tumors in TSC
Case-Control
2022-05-09
phs002915
Integrative Single-Cell Analysis of Transcriptome, Epigenome, and Lineage in HIV Latency and Activation
Case-Control
2022-05-09
phs002919
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): REasons for Geographic and Racial Differences in Stroke (REGARDS)
Longitudinal Cohort
2022-05-11
phs002921
Whole Genome Sequencing in the Inner City Asthma Consortium (ICAC) Cohorts
Longitudinal
2023-01-10
phs002922
Genomic and Transcriptomic Sequencing of CAR-T-Treated Patients
Cohort
2022-05-13
phs002925
Genomic Analysis of Extra-Nodal Natural Killer/T-Cell Lymphoma (ENKTCL)
Exome Sequencing
2022-05-18
phs002926
Infant Immune Responses to Early Life Vaccinations
Clinical Cohort
2022-05-18
phs002928
Adoptive Cell Therapy of Autologous T cell Receptor-Engineered T Cells Targeting the p53 Neoantigens in Human Solid Tumors
Clinical Trial
2022-05-19
phs002929
The Genetic Basis of Progression in Multiple Sclerosis
GWAS
2022-05-19
phs002931
Decade-Long Leukemia Remissions with Persistence of CD4+ CAR T-Cells
Case Set
2022-05-23
phs002933
Single-Cell RNA-Sequencing Analysis of Responses to Pembrolizumab in Sezary Syndrome
Single Cell Analysis
2022-05-24
phs002934
Molecular Biomarkers of Obesity and Metformin Response in Endometrial Cancer: Analysis of GOG-0286B
Case Set
2022-05-25
phs002935
Transcriptomic Profiling of Oropharyngeal Squamous Cell Carcinoma
Case Set
2022-05-25
phs002937
Exploring the Genomic Dark Matter of Neurodevelopmental Disorders
Case-Control
2022-06-01
phs002939
NCI-Maryland Prostate Cancer Case-Control Study
Case-Control
2022-06-04
phs002940
PRE-DETERMINE: Biologic Markers and MRI SCD Cohort Study
Longitudinal Cohort
2022-06-06
phs002941
CALGB/SWOG 80405 ct DNA Biomarker Evaluation
Longitudinal
2022-06-06
phs002944
Melanoma Brain Metastasis Single-Cell RNA Sequencing Atlas
Cohort
2022-06-07
phs002950
Methylation Profiles of Cell-Free DNA Using Nanopore Sequencing
Case-Control
2022-06-09
phs002959
Joslin Study on the Genetics of Type 2 Diabetes
Family
2022-06-14
phs002960
Exploring the Microbiome-Gut-Brain Axis with Respect to Psychoneurological Symptoms for Children with Solid Tumors
Case-Control
2022-06-14
phs002962
Germline Genetics of Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML)
Case-Control
2022-06-15
phs002966
Single-Cell Analysis of CD19-Specific CAR T Cell Treatment of Relapsed/Refractory CD19+ Acute Lymphoblastic Leukemia
Clinical Cohort
2022-06-17
phs002968
Inherited T Cell Defects: Diagnosis, Mechanisms and Treatments
Exome Sequencing
2022-06-18
phs002973
Genomic Translation for ALS Care (GTAC) - WGS
Case Set
2022-06-27
phs002977
Functional Analysis of Genetic Variants in African Americans with Breast Cancer
Affected Sib Pairs
2022-06-29
phs002978
AC-ICAM: An Atlas and Compass of Immune-CAncer-Microbiome Interactions in Colon Cancer
Case-Cohort
2022-06-29
phs002979
Evaluation of Nuclear DNA from Rootless Hairs for Forensic Purposes
Genotype
2022-06-29
phs002980
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Mediators of Atherosclerosis in South Asians Living in America Study (MASALA)
Cohort
2022-06-30
phs002981
INCLUDE: Human Trisome Project
None
2022-06-30
phs002982
INCLUDE: The Epidemiology of Transient Leukemia in Newborns with Down Syndrome
None
2022-06-30
phs002983
INCLUDE: Genetic Underpinnings of the Multifactorial Phenotype of Trisomy 21 Patients Unveiled by Multi-Omics Approaches
None
2022-06-30
phs002985
Center for Common Disease Genomics [CCDG] - Cardiovascular: Pharmacokinetic Polymorphisms in Japanese General Population
Control Set
2022-07-05
phs002986
A Randomized Multi-Institutional Phase II Trial of Everolimus as Adjuvant Therapy in Patients with Locally Advanced Squamous Cell Cancer of the Head and Neck
Case Set
2022-07-05
phs002988
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Atherosclerosis Risk in Communities Study (ARIC)
Longitudinal Cohort
2022-07-06
phs002989
Genomic Analysis of Follicular Lymphoma
Case Set
2022-07-06
phs002990
Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency
Exome Sequencing
2022-07-07
phs002991
Improving Transcriptome Fidelity Following Synovial Tissue Disaggregation
Case Set
2022-07-12
phs002994
BRCA Mutation Status Shapes the Microenvironment of Pancreatic Adenocarcinoma
Cohort
2022-07-15
phs002996
Biological Determinants of Peritoneal Dialysis Outcomes
GWAS
2022-07-19
phs002997
Genetic Analysis of Syndromic Orofacial Clefting
Case-Control
2022-07-20
phs002998
Immune Profiles Study
Case Set
2022-07-21
phs002999
Uncovering Inversion Formation in the Human Genome and its Impact to Disease
Case Set
2023-10-31
phs003000
ALLELE Consortium Glioblastoma Project
Case-Control
2022-07-25
phs003001
Assessment of RNA-Seq Sample Preparation Methodology
Case-Control
2022-07-26
phs003002
A Platform Study of Combination Immunotherapy for the Neoadjuvant and Adjuvant Treatment of Patients with Surgically Resectable Adenocarcinoma of the Pancreas
Clinical Trial
2022-07-26
phs003003
Gene Expression between PMD and Control LCLs at Baseline, E2, and E2 Withdrawal
Case-Control
2022-07-26
phs003005
Somatic Mutations in Single Human Neurons from Patients with Congenital Neurodegenerative Diseases
Single Cell Analysis
2022-07-31
phs003006
Transcriptional and Epigenetic Profiles of Male Breast Cancer at Single-Cell Resolution Nominate Salient Cancer Specific Enhancers
Case Set
2022-08-01
phs003009
Genomic Characterization of Duke Melanoma Brain Metastases
Case Set
2022-08-02
phs003010
Center for Common Disease Genomics [CCDG] - Cardiovascular: TexGen
Case Set
2022-08-02
phs003011
APOLLO1: Proteogenomic Analysis of Lung Adenocarcinoma
Tumor
2022-08-02
phs003014
NCI's Datasets for General Research Use
None
2022-08-04
phs003015
Ipilimumab and Decitabine in Treating Patients With Relapsed or Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia
Clinical Trial
2022-08-04
phs003016
Coagulation and Fibrinolysis in a Pediatric Insulin Titration Trial
Clinical Trial
2022-08-04
phs003017
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Multi-Ethnic Study of Atherosclerosis (MESA)
Longitudinal Cohort
2022-08-04
phs003019
Phase I Study of the Oral PI3kinase Inhibitor BKM120 or BYL719 and the Oral PARP Inhibitor Olaparib in Patients with Recurrent Triple Negative Breast Cancer or High Grade Serous Ovarian Cancer
Clinical Trial
2022-08-07
phs003020
Molecular Analysis of Short- Versus Long-Term Survivors of High-Grade Serous Ovarian Carcinoma
Copy Number Variation (CNV)
2022-08-09
phs003022
Circulating Tumor DNA Sequencing Provides Comprehensive Mutation Profiling for Pediatric Central Nervous System Tumors
Cohort
2022-08-12
phs003023
Whole-Genome Sequencing Reveals Complex Genomic Features Underlying Anti-CD19 CAR T-Cell Treatment Failure in Lymphoma
Whole Genome Sequencing
2022-08-12
phs003024
Gene Expression Analysis in Clonal Evolution of Fanconi Anemia
Case Set
2022-08-12
phs003025
Genetic Analysis of Substance Use Disorder Using the Indiana Biobank Data
Case-Control
2022-08-15
phs003028
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Northern Manhattan Study (NOMAS)
None
2022-08-15
phs003035
Genomic Analysis of Nucleic Acid Sequences from Pancreatic Cancer
Sequencing
2022-08-18
phs003036
Single Cell Genome Variation Induced by Mutational Processes in Cancer - HGSOC Trios Study
Tumor vs. Matched-Normal
2022-08-18
phs003038
Exploiting New Patterns of Genome Damage in Triple Negative Breast Cancer
Tumor vs. Matched-Normal
2022-08-19
phs003041
Mayo Clinic Adult Diffuse Glioma Illumina OncoArray SNP data
Case Set
2022-08-22
phs003042
Novel Strategies to Eliminate Resistance to B-cell Receptor Inhibitor Therapy in Lymphoid Malignancies
Case Set
2022-08-24
phs003043
A Pilot Study to Evaluate Tissue- and Plasma-based DNA Driver Mutations in a Cohort of Patients with Pancreatic Intraductal Papillary Mucinous Neoplasms
Sequencing
2022-08-24
phs003044
NCI's Collection of Datasets for Health, Medical, and Biomedical Research Purposes
None
2022-08-24
phs003046
Epigenetic Biomarkers of Aging
Epigenetics
2022-08-30
phs003047
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Case Set
2022-08-31
phs003048
Juvenile Sjogren's Syndrome (JSS) Transcriptome Study
Case-Control
2022-09-01
phs003053
Resilience and Susceptibility Patterns in the Viral Immune Response Using RNA-Seq (ReSP VIRUS Study)
Cross-Sectional
2022-09-06
phs003054
Extracellular RNA Profiling of Serum, Plasma, and Urine of Healthy Subjects
Longitudinal
2022-09-09
phs003059
Metastatic Colorectal Adenocarcinoma Tumor Purity Assessment from Whole Exome Sequencing Data
Case Set
2022-09-13
phs003060
Whole Exome Sequencing of Calcitonin Producing Pancreatic Neuroendocrine Neoplasms (CT-pNENs) Indicates a Unique Molecular Signature
Clinical Cohort
2022-09-14
phs003062
De Novo Characterization of Cell-Free DNA Fragmentation Hotspots in Plasma Whole-Genome Sequencing
Case-Control
2022-09-16
phs003063
COVID-19: Post-Hospital Thromboprophylaxis A Multicenter, Adaptive, Prospective, Randomized Trial Evaluating the Efficacy and Safety of Antithrombotic Strategies in Patients with COVID-19 Following Hospital Discharge (ACTIV-4C)
Clinical Trial
2022-09-16
phs003064
Phenotypic Signatures of Circulating Neoantigen-Reactive CD8+ T Cells in Patients with Metastatic Cancers
Case Set
2022-09-19
phs003065
Uncovering RNA Signatures of C9orf72-Linked ALS and Related Disorders
Case-Control
2022-09-20
phs003066
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): A Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study
Prospective
2022-09-22
phs003067
Using NGS to Sequence Whole Genomes to Identify Genes Underlying ALS
Case-Control
2022-09-22
phs003068
Nanobody-Tethered Transposition Allows for Multifactorial Chromatin Profiling at Single-Cell Resolution
Epigenetics
2022-09-26
phs003070
Single Cell RNA-Sequencing in Adenoid Cystic Carcinoma
Case Set
2022-09-30
phs003071
POISED (Peanut Oral Immunotherapy: Safety, Efficacy, and Discovery)
Clinical Trial
2022-10-01
phs003072
RNA-Seq of Whole Blood from Patients with Intracranial Aneurysms
Collection
2022-10-03
phs003074
A National Translational Science Network of Precision-Based Immunotherapy for Primary Liver Cancer (PLC)
Longitudinal
2022-10-04
phs003075
Longitudinal Studies of Patients with Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)
Exome Sequencing
2022-10-04
phs003077
Retinoblastoma Aqueous Humor Liquid Biopsy Repository
Clinical Cohort
2022-10-06
phs003079
Spatiotemporal Evolution of the ccRCC Microenvironment Links Intra-Tumoral Heterogeneity to Immune Escape CINOMA
Clinical Trial
2022-10-07
phs003080
Cell and Circuit-Specific Exploration of HIV Neurogenomics in Context of Opiate and Cocaine Misuse
Epigenetics
2022-10-10
phs003084
Genome Sequencing of Circulating Tumor Cells for Minimally Invasive Molecular Characterization of Multiple Myeloma Pathology
Tumor vs. Matched-Normal
2022-10-12
phs003085
RNA-Sequencing of B-Lymphoblastic Leukemia with Glucocorticoids and PI3K Delta Inhibition
Case Set
2022-10-12
phs003086
Single Cell Transcriptomic Data from CD4+ T Cells from Children with MIS-C
Case-Control
2022-10-13
phs003090
Advancing Precision Oncology in a Humanized, Fully Autologous Mouse Model
Cohort
2022-10-14
phs003091
Single-Cell DNA Methylation Profiling with sciMETv2
Epigenetics
2022-10-18
phs003093
The Genomic Landscape of Interval Colorectal Cancers
Exome Sequencing
2022-10-19
phs003094
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): a Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study - for Samples Collected at Johns Hopkins
Prospective
2022-10-19
phs003095
Transcriptomic Analysis of HIV-Infected Cells
Clinical Cohort
2022-10-19
phs003096
African Demographic History Study Based on WGS Data
Cohort
2022-10-19
phs003097
Multi-Modal Single-Cell and Whole-Genome Sequencing of Small, Frozen Clinical Specimens
Cohort
2022-10-20
phs003099
Integration of Clinical and Molecular Biomarkers for Melanoma Survival (Berwick)
Case-Control
2022-10-21
phs003100
Whole-Genome Sequencing Analysis of Extrachromosomal DNA with Amplicon Architect
Tumor
2022-10-24
phs003101
A Model of Human Asthma Exacerbation Identifies Mechanisms That Drive Allergic Asthma
Case-Control
2022-10-24
phs003103
Single Cell Analysis of Sporadic Human Basal Cell Carcinomas
Case Set
2022-10-25
phs003105
Genetic and Phenotypic Analysis of Multiple Sclerosis in Hispanics
Case-Control
2022-11-01
phs003106
Genetic Effects on miRNA Expression During Mid-Gestation Neocortical Development
eQTL
2022-11-02
phs003108
Role of Genetic Factors in the Pathogenesis of Lung Disease
Case Set
2022-11-03
phs003109
Oral Immunotherapy for Induction of Tolerance and Desensitization in Peanut-Allergic Children (IMPACT)
Clinical Trial
2022-11-04
phs003110
Clonally selected lines after CRISPR/Cas editing are not isogenic
Case Set
2022-11-07
phs003111
Childhood Cancer Data Initiative (CCDI): Clonal Evolution During Metastatic Spread in High-Risk Neuroblastoma
Longitudinal Cohort
2022-11-09
phs003112
Transcriptomics of Liver and PBMCs in Alcohol-Associated Liver Disease
Case-Control
2022-11-09
phs003115
Genetics of Male Infertility Initiative (GEMINI)
Exome Sequencing
2022-11-14
phs003117
Multiregional Single-Cell Transcriptomic Analysis of Liver Cancer
Case Set
2022-11-15
phs003121
Targeted Genomic Sequencing in Large Human Genes to Detect Induced Structural Variants
Copy Number Variation (CNV)
2022-11-20
phs003122
Human Blastocyst 10X Single Cell RNA Sequencing
RNA Sequencing
2022-11-21
phs003131
NHLBI's Collection of Datasets for General Research Use (Public Posting of Genomic Summary Results: Not Allowed)
Collection
2022-11-23
phs003132
NHLBI's Collection of Datasets for General Research Use (Public Posting of Genomic Summary Results: Allowed)
None
2022-11-23
phs003133
NHLBI's Collection of Datasets for Health / Medical / Biomedical Research Use (Public Posting of Genomic Summary Results: Not Allowed)
Collection
2022-11-23
phs003134
NHLBI's Collection of Datasets for Health / Medical / Biomedical Research Use (Public Posting of Genomic Summary Results: Allowed)
None
2022-11-23
phs003136
African American Adolescent Idiopathic Scoliosis Whole Genome and Whole Exome Study
Case Set
2022-11-23
phs003138
3/7 Psychiatric Genomics Consortium: Finding Actionable Variation
Case-Control
2022-11-28
phs003139
Genetic Progression of Head and Neck Squamous Cell Carcinoma
Cohort
2022-11-28
phs003140
Genetic Epidemiology of Ovarian Cancer Histotypes
Case Set
2022-11-29
phs003141
Integrative Somatic and Germline Computational Biology to Redefine Clinical Actionability in Solid Tumors
Case Set
2022-12-06
phs003143
My Pediatric and Adult Rare Tumor (MyPART) Natural History Study of Rare Solid Tumors
Clinical Cohort
2022-12-06
phs003145
Tissue Sampling and Biorepository to improve Cancer Cell Therapy
Case Set
2022-12-07
phs003146
Predicting the Prevalence of Complex Genetic Diseases from Individual Genotype Profiles Using Capsule Networks
Genotype
2022-12-07
phs003147
A Phase II Neoadjuvant Study of Palbociclib in Combination with Letrozole and Trastuzumab as Neoadjuvant Treatment of Stage II-III ER+ HER2+ Breast Cancer (PALTAN)
Clinical Trial
2022-12-07
phs003148
NCT03343197: Clinical Biomarker Data
Clinical Trial
2022-12-07
phs003149
Bladder Cancer Organoids as a Functional System to Model Different Disease Stages and Therapy Response
Case Set
2022-12-07
phs003150
International Cancer Proteogenomics Consortium (ICPC): Proteogenomics of East-Asian Breast Cancer
Exome Sequencing
2022-12-07
phs003151
Genetics of Glucose Regulation in Gestation and Growth (Gen3G) Cohort - Placenta Transcriptomics RNA Sequencing
Cohort
2022-12-08
phs003152
CPTAC: Proteogenomic Studies of Ovarian Tumor Responses to Agents Targeting the DNA Damage Response
Case Set
2022-12-08
phs003153
Neoantigen-Targeted CD8+ T-Cell Responses 1 With PD-1 Blockade Therapy
Case Set
2022-12-12
phs003154
An Advanced Molecular Medicine Case Report of a Rare Human Tumor Using Genomics, Pathomics, and Radiomics
Case-Control
2022-12-14
phs003155
TCGA WGS Variants Across 18 Cancer Types
GWAS
2022-12-15
phs003156
Developing Biomarkers Incorporating High Throughput RNA, DNA, Small RNA Sequencing and Protein Expression in Inflammatory Bowel Disease Using Formalin-Fixed, Paraffin-Embedded (FFPE) Tissue Samples
Case-Control
2022-12-15
phs003158
Sézary Syndrome Originates from Heavily Mutated Hematopoietic Progenitors
Case Set
2022-12-19
phs003159
Targeted Long-Read Sequencing of the Ewing Sarcoma 6p25.1 Susceptibility Locus
Case-Control
2022-12-20
phs003165
Phase I Study and Cell-Free DNA Analysis of T-DM1 and Metronomic Temozolomide for Secondary Prevention of HER2-Positive Breast Cancer Brain Metastases
Case Set
2022-12-22
phs003166
Enhancing Open Data Sharing for Functional Genomics Experiments: Measures to Quantify Genomic Information Leakage and File Formats for Privacy Preservation
Genotype
2022-12-25
phs003168
Phenotypic and Genotypic Study of Keratoconus
Case Set
2022-12-27
phs003169
Extracellular microRNA Biomarkers for Diagnostic and Prognostic Assessment of Preeclampsia at Triage
Case-Control
2022-12-27
phs003170
Genome-Wide Analysis of Aberrant Position and Sequence of Plasma DNA Fragment Ends in Patients With Cancer
Case-Control
2022-12-31
phs003172
Malnutrition and Enteric Disease Network (Mal-ED) Birth Cohort in Brazil
Prospective
2023-01-10
phs003173
Malnutrition and Enteric Disease Network (Mal-ED) Case-Control Study in Brazil
Prospective
2023-01-10
phs003174
Intervention with Micronutrients and Long-Term Impact in Brazil-RECODISA
Prospective
2023-01-10
phs003175
Long-term Impact and Intervention with Micronutrients in Brazil, Parque Universitário, Community-Based Study
Randomized
2023-01-10
phs003177
Comparison Between qPCR and RNA-Seq Reveals Challenges of Quantifying HLA Expression
Genotype/Expression
2023-01-11
phs003179
Rheumatoid Arthritis Finger Stick RNA Sequence Data
Observational
2023-01-12
phs003182
Reference Profiles of ExRNAs in Normal Human Pregnancy
Case-Control
2023-01-20
phs003183
The Ultrasound Study of Tamoxifen
Cohort
2023-01-20
phs003184
ALS Compute
Case-Control
2023-01-20
phs003185
Molecular Subtyping Reveals Immune Alterations Associated with Progression of Bronchial Premalignant Lesions
Clinical Cohort
2023-01-24
phs003186
Tamoxifen Response at Single Cell Resolution in Estrogen Receptor Positive Primary Human Breast Tumors
Case Set
2023-01-26
phs003187
LCLF1.0 Data
RNA Sequencing
2023-01-27
phs003188
Overcoming Clinical Resistance to EZH2 Inhibition Using Rational Epigenetic Combination Therapy
Clinical Cohort
2023-01-27
phs003190
Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and is Associated with Worse Outcomes
Observational
2023-01-31
phs003191
RNA Splicing Dysregulation in the Pathogenesis of Chronic Lymphocytic Leukemia
Cohort
2023-01-31
phs003192
ARST17B2-Q Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Case Set
2023-02-03
phs003194
Maternal and Developmental Risks from Environmental and Social Stressors (MADRES) Center for Environmental Health Disparities
Cohort
2023-02-06
phs003195
NSD2 E1099K Drives Relapse in Pediatric Acute Lymphoblastic Leukemia by Disrupting 3D Chromatin Organization
Phase III
2023-02-07
phs003196
Detection and Targeting of Splicing Deregulation in Pediatric Acute Myeloid Leukemia Stem Cells
Case-Control
2023-02-07
phs003197
Genetic Study of Vascular Anomalies
Case Set
2023-02-08
phs003198
Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer
Case Set
2023-02-08
phs003199
RNA-Seq Data From Early Stage Triple Negative Breast Cancer Tumors Treated With TVEC and Chemotherapy (MCC18621)
Case Set
2023-02-08
phs003200
High-Throughput RNA Isoform Sequencing using Programmable cDNA Concatenation
Methods Development
2023-02-10
phs003201
E5103 Correlative Studies
Case-Control
2023-02-13
phs003202
Joint Addiction, Aging, and Mental Health (JAAMH) Data Access Committee General Research Use Datasets
Collection
2023-02-13
phs003203
A Comprehensive Platform for Analyzing Longitudinal Multi-Omics Data
Epigenetics
2023-02-13
phs003207
Single Cell Colony Whole Genome Sequencing Data From Individuals With Telomere Syndromes
Case-Control
2023-02-14
phs003208
Transcriptomic Profiling of Bulk Tissue and Laser-Capture Microdissected Neurons of Postmortem Human Brains in the Superior Temporal Gyrus
RNA Sequencing
2023-02-14
phs003209
Structurally Complex Osteosarcoma Genomes Exhibit Limited Heterogeneity within Individual Tumors and across Evolutionary Time
Copy Number Variation (CNV)
2023-02-15
phs003210
The Nephrotic Syndrome Study Network (NEPTUNE)
Longitudinal Cohort
2023-02-16
phs003212
A Pilot Trial of Complement Inhibition Using Eculizumab to Overcome Platelet Transfusion Refractoriness in HLA Allo-Immunized Patients
Clinical Trial
2023-02-23
phs003213
Melbourne Collaborative Cohort Study DNA Methylation Studies
Longitudinal
2023-02-24
phs003214
NPC Genome Project
Case Set
2023-02-24
phs003216
Whole Genome Sequencing Analysis in a Family of Discordant Twins With Non-Syndromic Microtia and Hemifacial Microsomia: Identification of Novel Candidate Genes and Variants
Case-Control
2023-03-01
phs003217
Molecular Determinants of Esophageal Cancer in Tanzania
Cohort
2023-03-01
phs003218
Whole Exome Sequencing and RNA-Seq to Characterize the Somatic Breast Cancer Landscape Among Latinas in California
Case Set
2023-03-02
phs003221
Sudden Death in the Young Case Registry
Case Set
2023-03-07
phs003223
DIGEST: Dietary Influences on Glucuronidation, a Cross-Sectional Study of Diet and Metabolism
Control Set
2023-03-09
phs003227
Hi-C Profiling of Solid Tumor Samples
Case Set
2023-03-13
phs003228
Genomics of Blastic Plasmacytoid Dendritic Cell Neoplasm
Longitudinal
2023-03-13
phs003229
Analysis of Donor Pancreata Defines the Transcriptomic Signature and Microenvironment of Early Neoplastic Pancreatic Lesions
Observational
2023-03-17
phs003230
Temporal Evolution Reveals Bifurcated Lineages in Aggressive Neuroendocrine Small Cell Prostate Cancer Trans-Differentiation
Longitudinal
2023-03-17
phs003231
ApoA-1 and Atherosclerosis in Psoriasis
Longitudinal
2023-03-20
phs003233
Single Cell Genotypic and Phenotypic Analysis of Measurable Residual Disease in Acute Myeloid Leukemia
Clinical Genetic Testing
2023-03-22
phs003234
Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): COVID-19 Testing and Vaccination Social Network Diffusion for Diverse Criminal Legal Involved Communities
Controlled Trial
2023-03-22
phs003240
Binding of Epstein Barr Virus EBNA2 Unifies Multiple Sclerosis Genetic Mechanisms
Case-Cohort
2023-03-24
phs003242
TREM2+ Cells in Human Basal Cell Carcinomas
Case Set
2023-03-24
phs003243
Comprehensive Omics Analysis of Pediatric Solid Tumors and Establishment of a Repository for Related Biologic Studies (10C0086)
Observational
2023-03-25
phs003245
Phenotyping and Therapeutic Approaches for Patients with Sellar/Suprasellar Disorders
Case Set
2023-03-29
phs003246
Multimodal Immune Profiling to Determine Mechanisms of COVID-19 Clinical Trajectory in Uganda
Clinical Cohort
2023-03-30
phs003249
Deterministic Evolution and Stringent Selection During Pre-Neoplasia
Copy Number Variation (CNV)
2023-04-02
phs003250
Therapeutic Genetics and Disease Modeling in LAMA2-CMD
Interventional
2023-04-02
phs003255
Single Duplex DNA Sequencing with CODEC Detects Mutations with High Sensitivity
Case-Control
2023-04-07
phs003256
Therapy-Induced APOBEC3A Drives Evolution of Resistance to Targeted Therapies in Non-Small Cell Lung Cancer
Individual-Level Genomic Data
2023-04-10
phs003257
Investigating the Role of Neddylation in the Repair of Topoisomerase I-Mediated DNA Damage in Colorectal Cancer
Cohort
2023-04-11
phs003260
Single Nucleus Transcriptomes from the Ventral Midbrain of Opioid Overdose Cases and Controls
Cohort
2023-04-12
phs003261
Studies in the Pathogenesis of Systemic Capillary Leak Syndrome (SCLS, Clarkson Disease)
Case-Control
2023-04-13
phs003268
Maintenance of Brain Tumor Profile on Organotypic Brain Slice Culture (OBSC)
Case Set
2023-04-14
phs003269
GATA2 Deficiency and the MonoMAC Syndrome
Case-Cohort
2023-04-14
phs003270
Studies in the Natural History and Pathogenesis of Childhood-Onset and Adult-Onset Idiopathic Inflammatory Myopathies
Case-Control
2023-04-14
phs003272
Supraphysiologic MDM2 Expression Impacts P53-Independent Chromatin Networks and Therapeutic Responses in Sarcoma
Cohort
2023-04-17
phs003277
Cellular Indexing of Transcriptomes and Epitopes Sequencing (CITE-Seq) Analysis to Investigate the Impact of Granulocyte-Colony Stimulating Factor on CRISPR/Cas9 Gene Edited Human Hematopoietic Stem Cell Function
RNA Sequencing
2023-04-20
phs003278
Sex Chromosome Aneuploidy Effects on Human Gene Expression
Case-Control
2023-04-20
phs003279
MAITS in HCC
Single Cell Analysis
2023-04-24
phs003282
Genetic Analysis of Skin Cells
Aggregate Genomic Data
2023-04-26
phs003283
eIMPACT Trial: Modernized Collaborative Care to Reduce the Excess CVD Risk of Older Depressed Patients
Clinical Trial
2023-04-26
phs003284
Immune-Related Adverse Events after Immune Checkpoint Blockade-Based Therapy are Associated with Improved Survival in Advanced Sarcoma
Clinical Trial
2023-04-27
phs003286
CDKN2A Deletion Remodels Lipid Metabolism to Prime Glioblastoma for Ferroptosis
Exome Sequencing
2023-05-01
phs003287
FinaleMe: Predicting DNA Methylation by the Fragmentation Patterns of Plasma Cell-Free DNA
Epigenetics
2023-05-01
phs003288
Multi-Ethnic Study of Atherosclerosis (BioLINCC)
Family
2023-05-02
phs003290
Cell-Free, Methylated DNA in Blood Samples Reveals Tissue-Specific, Cellular Damage from Radiation Treatment
Epigenetics
2023-05-05
phs003297
Population Genetic Testing and SERPINA1 Sequencing Identifies Unidentified Alpha-1 Antitrypsin Deficiency Alleles and Gene-Environment Interaction with Hepatitis C Infection
Clinical Diagnostic Testing
2023-05-09
phs003298
Genetics and Functional Studies of Autosomal Recessive Neurological Disorders
Family
2023-05-11
phs003300
Small RNA Contents of Extracellular Vesicles from Patients with Cognitive Decline
Case-Control
2023-05-12
phs003302
Epigenetic Landscape of Human Parathyroids
Collection
2023-05-17
phs003303
Molecular and Clinical Analyses of PHF6 Mutant Myeloid Neoplasia Provide Clues as to Their Pathogenesis and Therapeutic Targeting
Cohort
2023-05-18
phs003306
Characterization of Macrophage-Tropic HIV Infection of Central Nervous System Cells and the Influence of Inflammation
Case Set
2023-05-19
phs003308
Whole Exome Sequencing Analysis of Carfilzomib-Related Cardiotoxicity in Multiple Myeloma Patients
Clinical Cohort
2023-05-23
phs003310
Type I Interferon and Cycling Lymphocytes in Macrophage Activation Syndrome
Case-Control
2023-05-25
phs003312
PD-1 Instructs a Tumor Suppressive Metabolic Program to Restrain AP-1 Activity in T Cell Lymphoma
Case Set
2023-05-26
phs003313
RNA-Seq from PMM2-CDG Patients and Healthy Controls
Case-Control
2023-05-31
phs003315
A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids
Copy Number Variation (CNV)
2023-05-31
phs003316
A Pilot Study of Neoadjuvant Nivolumab, Ipilimumab and Intralesional Oncolytic Virotherapy for HER2-Negative Breast Cancer
Cohort
2023-06-05
phs003317
Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking
Case-Control
2023-06-07
phs003318
Single-Cell Multi-Omic Analysis of the Vestibular Schwannoma Ecosystem Uncovers a Nerve Injury-Like State
Case Set
2023-06-08
phs003319
Interruption of BTK Inhibitor Improves Response to SARS-CoV-2 Booster Vaccination in Patients with Chronic Lymphocytic Leukemia
Clinical Cohort
2023-06-09
phs003320
RNA Sequencing of ECOG-E1308
Case Set
2023-06-13
phs003321
DNA Methylation Studies in CREW Cohorts (URECA and COAST)
Case-Control
2023-06-15
phs003322
Integrated Analysis of Multimodal Single-Cell Datasets for SARS-CoV-2 Vaccination
Sequencing
2023-06-19
phs003326
Microvascular Permeability, Inflammation, and Lesion Physiology in Endometriosis: A Microphysiological Systems Approach
Case-Control
2023-06-23
phs003327
Experimental and Clinical Studies of Presbycusis
Cohort
2023-06-26
phs003328
Genetic Causes of Congenital Anosmia
Case-Control
2023-06-27
phs003330
Uveal Melanoma Immunogenomics Predict Immunotherapy Resistance and Susceptibility
RNA Sequencing
2023-06-29
phs003338
BarcUVa-Seq (Biology of Colorectal Cancer Risk Enhancers)
Cohort
2023-07-03
phs003342
Meta-Analysis of Genome-Wide Association Studies of Bladder Cancer Risk
Case-Control
2023-07-11
phs003343
Targeted Linked-Read DNA-seq Analysis of Castration-Resistant Prostate Cancers
Case Set
2023-07-11
phs003346
Method to Assess Lung Water Accumulation During Exercise
Methods Development
2023-07-13
phs003349
Single-Cell Transcriptomics of Adult Recurrent Respiratory Papillomatosis
Case Set
2023-07-18
phs003350
Diabetes Multi-Omic Investigation of Drug Response (DIAMOND)
Longitudinal Cohort
2023-07-18
phs003358
Patient Microbiome and Surgical Site Infection in Spine Surgery
Case Set
2023-07-25
phs003361
Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): COVID-19 Testing and Prevention in Correctional Settings
Collection
2023-07-26
phs003369
Low-Dose Carboplatin Modifies the Tumor Microenvironment to Augment CAR T Cell Efficacy in Human Prostate Cancer Models
RNA Sequencing
2023-07-31
phs003370
Genetic Predictors of Ibrutinib-Related Cardiovascular Side Effects in Patients with Chronic Lymphocytic Leukemia
Case-Control
2023-08-01
phs003378
A Phase I Study of the Treatment of Recurrent Malignant Glioma with CAN-3110 (AKA rQNestin34.5v.2), a Genetically Engineered HSV-1 Virus
Clinical Cohort
2023-08-03
phs003381
Cryptic Splice Mutation in the Fumarate Hydratase Gene in Patients With Clinical Manifestations of Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC)
Case Set
2023-08-08
phs003389
Genomic Studies in Charcot-Marie-Tooth Disease
Case Set
2023-08-16
phs003390
Adipose Tissue Omics In Obesity
Case Set
2023-08-17
phs003392
Epigenetic Changes in Immune Response and Oncogenesis Related Genes Caused by Heavy Metal Long-Term Exposure
Case-Control
2023-08-18
phs003398
Non-Coding Mutations Cause Enhancer Targeting Resulting in Protein Synthesis Dysregulation During B-Cell Lymphoma Progression
Tumor vs. Matched-Normal
2023-08-18
phs003399
Reference Standards for Mosaic Variant Detection
Exome Sequencing
2023-08-19
phs003400
Dysregulation of Naive T Cell Quiescence during Aging
Cross-Sectional
2023-08-21
phs003402
Genomic Tumor Correlates of Clinical Outcomes Following Organ-Sparing Chemoradiation Therapy for Bladder Cancer
Case Set
2023-08-27
phs003403
Circulating RNAs in Acute Heart Failure (CRUCIAL)
Cohort
2023-08-28
phs003404
Genomic Analysis of Prostate Tumor Heterogeneity in Metastasis
Tumor vs. Matched-Normal
2023-08-29
phs003408
MILK-Omics: Systems Biology of Human Milk and Its Links to Maternal and Infant Health
Cohort
2023-08-30
phs003410
A Human Lymphoma Organoid Model for Evaluating and Targeting the Follicular Lymphoma Tumor Immune Microenvironment
Case Set
2023-09-01
phs003412
A Phase III Randomized Study of Nivolumab Plus Ipilimumab Versus Nivolumab in Stage IV Squamous Cell Lung Cancer
Controlled Trial
2023-09-07
phs003415
Resistance Development in Basal Cell Nevus Syndrome through the Basal to Squamous Transition
Case Set
2023-09-08
phs003416
Transcriptomic and Epigenetic Profiling of SCLC Patient Samples
Epigenetics
2023-09-11
phs003417
The Chromatin Landscape of Pathogenic Transcriptional Cell States in Rheumatoid Arthritis
Case Set
2023-09-12
phs003418
Altered Interactions between Circulating and Tissue-Resident CD8 T Cells with the Colonic Mucosa Define Checkpoint Inhibitor Colitis
Case-Control
2023-09-13
phs003422
Hereditary Gastric Cancer Syndromes: An Integrated Genomic and Clinicopathologic Study of the Predisposition to Gastric Cancer
Case Set
2023-09-19
phs003427
Single-Cell Profiling of Premature Neonate Airways Reveals a Continuum of Myeloid Differentiation
Single Cell Analysis
2023-09-25
phs003428
CALGB/SWOG 80405: Genome-Wide Association Study of Patients with Advanced or Metastatic Colorectal Cancer Treated with First-Line Chemotherapy Combined with Cetuximab and/or Bevacizumab
eQTL
2023-09-26
phs003429
Whole-Exome Sequencing Study of Diabetic Nephropathy
Case-Control
2023-09-27
phs003435
Circulating Genomic Determinants of Treatment Failure in Hodgkin Lymphoma
Case-Control
2023-10-03
phs003436
KRT17High/CXCL8+ Tumor Cells Display Both Classical and Basal Features and Regulate Myeloid Infiltration in the Pancreatic Cancer Microenvironment
Observational
2023-10-04
phs003442
Early Family Prevention of Adolescent Alcohol, Drug Use, and Psychopathology
Cross-Sectional
2023-10-10
phs003446
Profiling RNA Translation in Pediatric Medulloblastoma
RNA Sequencing
2023-10-16
phs003447
MAESTRO-Pool Enables Highly Parallel and Specific Mutation-Enrichment Sequencing for Minimal Residual Disease Detection in Cohort Studies
Case Set
2023-10-16
phs003448
Non-Coding Autoimmune Risk Variant Defines Role for ICOS in T Peripheral Helper Cell Development
Cross-Sectional
2023-10-17
phs003453
Investigating Genetics in Suspected Congenital Syndromes
Case Set
2023-10-19
phs003466
Breast Cancer in Blacks: Impact of Genomics, Healthcare Use and Lifestyle on Outcomes (BRIGHT)
Individual-Level Genomic Data
2023-11-03
phs003469
Genetic Markers of Lipids in Indians: A Validation Study of Most Relevant Findings of Genome-Wide Association Studies
Cross-Sectional
2023-11-07
phs003470
Unrelated Donor Reduced Intensity Bone Marrow Transplant for Children with Severe Sickle Cell Disease (BMT CTN-0601-BioLINCC)
Clinical Trial
2023-11-07
phs003473
Cellular and Molecular Investigations of Human Hearts
Control Set
2023-11-14
phs003474
A Missense SNP in the Tumor Suppressor SETD2 Reduces H3K36me3 and Mitotic Spindle Integrity in Drosophila
Case-Control
2023-11-16
phs003475
PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
Exome Sequencing
2023-11-16
phs003477
BPH Tissues for Cell Culture and Analysis - Spatial Transcriptomics Identifies Candidate Stromal Drivers of Benign Prostatic Hyperplasia
Case Set
2023-11-21
phs003483
Systolic Blood Pressure Intervention Trial (SPRINT-BioLINCC)
Clinical Trial
2023-12-02
phs003485
Germline Genome Sequencing from Patients with Early-Onset Merkel Cell Carcinoma
Whole Genome Sequencing
2023-12-05
phs003486
Acquired Cross-Resistance in Small Cell Lung Cancer Patient-Derived Xenografts
Xenograft
2023-12-06
phs003489
FLG LoF Variants are Associated with Atopic Dermatitis in an Early-Life Prospective Cohort
Case Set
2023-12-07
phs003495
Postmortem Analysis of the Caudate Nucleus in Schizophrenia
Case-Control
2023-12-12
phs003496
Utility of Capillary Blood in Gene Expression Studies
Methods Development
2023-12-12
phs003497
Combinatorial Indexed 10x Genomics Single-Cell ATAC-seq on Human Cerebral Cortex
Control Set
2023-12-14
phs003502
Single-Cell and Spatial Multi-Omics Highlight Effects of Anti-Integrin Therapy Across Cellular Compartments in Ulcerative Colitis
Case-Control
2023-12-19
phs003506
Heart Failure Network Aldosterone Targeted Neurohormonal Combined with Natriuresis Therapy - (HFN ATHENA-BioLINCC)
Clinical Trial
2023-12-20
phs003509
Protracted Neuronal Recruitment in the Temporal Lobe of Young Children
Control Set
2023-12-26
phs003510
Heart Failure Network - Effectiveness of Ultrafiltration in Treating People with Acute Decompensated Heart Failure and Cardiorenal Syndrome (HFN CARRESS - BioLINCC)
Clinical Trial
2023-12-28
phs003512
Identification of Host Genetic Factors That Are Determinant for the Development of Severe Forms of COVID-19
Case Set
2023-12-29
phs003521
Cell Type-Specific and Disease-Associated eQTL in the Human Lung
Case-Control
2024-01-09
phs003524
Heart Failure Network: Diuretic Optimization Strategies Evaluation in Acute Heart Failure (HFN DOSE-BioLINCC)
Clinical Trial
2024-01-16
phs003529
Sickle Cell Disease Natural History Data Resource (SCD NHDR)
Clinical Cohort
2024-01-19
phs003531
A Prospective Study of Lifestyle, the Gut Microbiome, and Diverticulitis
Case-Control
2024-01-20
phs003533
Heart Failure Network - Xanthine Oxidase Inhibition for Hyperuricemic Heart Failure Patients (HFN EXACT-BioLINCC)
Clinical Trial
2024-01-24
phs003535
Integrating Genomic and Transcriptomic Data to Identify Breast Cancer Susceptibility Genes
Genotype
2024-01-26
phs003541
Identification of Novel Therapeutic Targets for Calcific Aortic Valve Stenosis Using Integrative Genomics
RNA Sequencing
2024-02-05
phs003543
National Sleep Research Resource (NSRR): Hispanic Community Health Study/Study of Latinos
Cohort
2024-02-06
phs003546
Gene Expression and Biomarker Utility in Post-Mortem Samples
Methods Development
2024-02-07
phs003561
Spatial Transcriptomics Reveals Discrete Tumor Microenvironments and Autocrine Loops Within Ovarian Cancer Subclones
Tumor
2024-02-21
phs003562
Action to Control Cardiovascular Risk in Diabetes (ACCORD - Imaging)
Clinical Trial
2024-02-22
phs003566
Systolic Blood Pressure Intervention Trial (SPRINT-Imaging)
Clinical Trial
2024-02-22