-
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
-
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 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
-
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
-
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
-
Genomic diversity of the African-descent Makranis of Pakistan
Study
EGAS00001002558
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Study
EGAS00001003159
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Study
EGAS00001001184
-
Human Genetics 5, Genome Institute of Singapore.
Dac
EGAC00001000412
-
The Druze analysis group
Study
EGAS00001000963
-
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Study
EGAS00001001003
-
Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721
-
Malignant mesothelioma EWAS on European prospective study
Study
EGAS00001006432
-
Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Study
EGAS00001001314
-
Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia
Study
EGAS00001001315
-
Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
-
Functional analysis of GATA2 synonymous mutations
Study
EGAS00001003817
-
HLF COPD DNA Methylomics
Study
EGAS00001006603
-
Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Study
EGAS00001002592
-
Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
-
Epigenetic dynamics of monocyte to macrophage differentiation
Study
EGAS00001001595
-
The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program 'CASCADE'
Study
EGAS00001002153
-
Case Report: early contribution of germline and nevi genetic alterations to a rapidly-progressing Cutaneous Melanoma Patient
Study
EGAS00001006459
-
Genomic landscape of oral cancers (Complete Genomics WGS)
Study
EGAS00001002393
-
Population Structure and Genetic Diversity in Argentinean populations
Study
EGAS00001001663
-
Comparison of HCC cell lines and primary HCCs
Study
EGAS00001001678
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
Genetic sequencing of MODY patients.
Study
EGAS00001001699
-
Whole exome sequencing of 76 individuals with familial atrial fibrillation
Study
EGAS00001003207