-
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.
Study
EGAS00001000455
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
Egypt_Genome_Project___low_coverage_whole_genome_sequencing
Study
EGAS00001000480
-
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000492
-
Autozygosity_pilot___Pakistani_from_Birmingham
Study
EGAS00001000511
-
Triple_Negative_Breast_Cancer_RNA_Sequencing
Study
EGAS00001000377
-
Autozygosity_pilot___British_Pakistani_from_Birmingham_2
Study
EGAS00001000567
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
HipSci-Whole Exome sequencing-healthy volunteers
Study
EGAS00001000592
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
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
Study
EGAS00001000417
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing
Study
EGAS00001000680
-
Autozygosity_pilot_Born_in_Bradford
Study
EGAS00001000462
-
Bone_Cancer___Rare_Types_Whole_Genome
Study
EGAS00001000501
-
Genetic_factors_underlying_premature_MI_in_Greek_families_without_vessel_disease
Study
EGAS00001000478
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
miRNA_expression_in_response_to_LPS_stimulus_in_macrophages
Study
EGAS00001000691
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
-
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Study
EGAS00001000682
-
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)
Study
EGAS00000000115
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
Paroxysmal neurological disorders
Study
EGAS00001000048
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
UK10K NEURO ASD MGAS
Study
EGAS00001000113
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
UK10K_RARE_HYPERCHOL
Study
EGAS00001000129
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
UK10K NEURO GURLING
Study
EGAS00001000225
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
-
Genetic landscape of pediatric Adrenocortical Tumor
Study
EGAS00001000257
-
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Study
EGAS00001000426
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349
-
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Study
EGAS00001000379
-
Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons
Study
EGAS00001000382
-
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)
Study
EGAS00001000416
-
Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Study
EGAS00001000460
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Study
EGAS00001000622
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
-
Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes
Study
EGAS00001007157
-
Dataset that contains runs of submission 12
Dataset
EGAD50000000040
-
Dataset that contains runs of submission 14
Dataset
EGAD50000000044
-
Genetic scoring guide for personalized risk assessment in pediatric B-cell precursor Acute Lymphoblastic Leukemia
Study
EGAS00001007239
-
Dataset that contains runs of submission 19
Dataset
EGAD50000000086
-
Genetic architecture of autism spectrum disorder in India
Dataset
EGAD00001008621
-
Dataset that contains runs of submission 15
Dataset
EGAD50000000082
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
-
Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome
Study
EGAS00001006643
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Study
EGAS00001007059
-
Single-cell study of 14 childhood medulloblastoma patients
Dataset
EGAD00001009057
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - WGS
Dataset
EGAD00001010872
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - TGS
Dataset
EGAD00001010874
-
Dataset that contains runs of submission 27
Dataset
EGAD50000000112
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
Genomic and transcriptomic data of glioma specimens
Dataset
EGAD00001006299
-
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Study
EGAS00001007002
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Submission 84 - study_title 1
Study
EGAS50000000120
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010913
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
-
Cologne University Hospital, Institute of Human Genetics, Pathomechanisms of Rare Kidney Diseases Research Group DAC
Dac
EGAC00001003295
-
GDAP - Genome Diversity in Africa Project (2021-02-12)
Dataset
EGAD00001006965
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Dataset
EGAD00001011067
-
Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
-
Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Dataset
EGAD00001011260
-
Cancer Genetics Data Access Commitee
Dac
EGAC00001001742
-
Longitudinal RNA-seq datasets from patients after abdominal surgery
Dataset
EGAD00001011102
-
Genetics of gene expression in primary human immune cells Data Access Committee
Dac
EGAC00001003318
-
Genetics of gene expression in primary human immune cells Data Access Committee
Dac
EGAC00001003327
-
Enhancer-gene rewiring in the pathogenesis of Quebec Platelet Disorder
Study
EGAS00001004315
-
The Haemgen RBC study
Study
EGAS00000000132
-
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
Study
EGAS00000000056
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Study
EGAS00001002517
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
Kibbutzim Family study
Study
EGAS00001002782
-
Molecular analysis of giant cell lesions
Study
EGAS00001002910
-
BLUEPRINT DNase accessibility (NCMLS)
Study
EGAS00001000351
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Whole-exome sequencing of acute erythroid leukemia
Study
EGAS00001003696
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719