-
Multiple Myeloma ChipSeq data on six histone modifications
Dataset
EGAD00001008353
-
Mixture of 2 (closer mtDNA)
Dataset
EGAD00001008727
-
Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
-
Epigenetic age deceleration reflects fitness improvements following a six-month endurance exercise intervention
Study
EGAS00001008221
-
Investigating the Role of Neddylation in the Repair of Topoisomerase I-Mediated DNA Damage in Colorectal Cancer
Study
phs003257
-
Combined single-cell transcriptomics and T-cell receptor sequencing reveal heterogeneity of mycosis fungoides between and within patients and identify a CD4+ cytotoxic subtype
Study
EGAS50000000226
-
Timing the landmark events in the evolution of clear cell renal cell cancer
Dataset
EGAD00001003445
-
Genomic Sequencing of Lung Adenocarcinoma
Study
phs000488
-
Cystic fibrosis multi-omics study
Study
EGAS00001006421
-
Warfarin Pharmacogenetics: Pharmacogenetic Optimization of Anticoagulant Response (POAT) and Genetic and Environmental Determinants of Warfarin Response (GEDWR)
Study
phs000708
-
Efficacy of two different FGFR-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation
Dataset
EGAD50000000021
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Heart Failure Network Aldosterone Targeted Neurohormonal Combined with Natriuresis Therapy - (HFN ATHENA-BioLINCC)
Study
phs003506
-
Feasibility study of enzymatic methylation sequencing of cell-free DNA from cerebrospinal fluid of pediatric brain tumors for classification
Study
EGAS50000000871
-
RNA-Seq of Whole Blood from Pediatric Sickle Cell Anemia (SCA) Patients
Study
phs002687
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
-
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Lung cohort
Study
EGAS00001004447
-
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Breast cohort
Study
EGAS00001004446
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004413
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004414
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004416
-
10X single-cell Multiome (RNA+ATAC) and single-cell RNAseq of xenograft-derived HSPC, progenitors and myeloid progeny
Dataset
EGAD50000002328
-
Single-Gene vs. Panel Sequencing in Advanced HR+/HER2− Breast Cancer
Study
EGAS00001008200
-
Genomic Profiling of Pediatric Tumors by Cell Free DNA Sequencing
Study
EGAS50000000072
-
eccDNA in maternal plasma
Study
EGAS00001003827
-
Whole-transcriptome sequencing of hepatocellular carcinoma biopsies (TACE study)
Study
EGAS00001005558
-
Data Use Ontology (DUO)
Documentation
access/data-access-committee/data-use-ontology
-
GDAP___Genome_Diversity_in_Africa_Project
Study
EGAS00001003602
-
Single-cell and bulk RNA-sequencing of nivolumab-treated glioblastoma
Study
EGAS00001007110
-
Meta-Analysis of Genome-Wide Association Studies of Bladder Cancer Risk
Study
phs003342
-
The NCAA-DoD Concussion Assessment, Research, and Education (CARE) Consortium
Study
phs002175
-
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Study
EGAS00001007327
-
Sequencing data from MethylScan assay on plasma
Study
EGAS00001008127
-
dbGaP Collection: Open Translational Science in Schizophrenia (OPTICS)
Study
phs000887
-
PAH sequencing study
Study
EGAS00001005532
-
Atherosclerosis Risk in Communities Study (ARIC-BioLINCC)
Study
phs003738
-
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS)
Dataset
EGAD00001001901
-
Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA
Study
JGAS000231
-
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Study
phs001037
-
Low T cell diversity is associated with poor outcome in bladder cancer - Bulk TCRseq data
Study
EGAS50000000940
-
A Scalable, GMP-Compatible, Autologous Organotypic Cell Therapy for Dystrophic Epidermolysis Bullosa
Study
phs003271
-
Variant calling from CC220-MM-001 cohorts A,B,D
Dataset
EGAD50000000388
-
Transcriptome profiling of megakaryocytes and platelets: application to GP9- and IKZF5-related thrombocytopenia
Study
EGAS50000001276
-
Epigenomic dataset of Human Hepatocellular Carcinoma for EpiHK
Study
EGAS50000000039
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
Genomics of Glomerular Disorders
Study
phs002480
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
Losartan Effects on Emphysema Progression (LEEP-BioLINCC)
Study
phs004313
-
Multi-omics analysis of treated cancer samples
Dataset
EGAD50000000349
-
Whole-exome sequencing data of ovarian clear cell carcinoma in East Asia
Study
EGAS50000000031
-
Genomic subtypes and cellular phenotypes of high-grade endometrial carcinoma
Study
JGAS000753
-
Genome sequencing of biliary tract cancers
Study
JGAS000109
-
Genome sequencing of biliary tract cancers
Study
JGAS000389
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
MutWP4: CRUK Grand Challenge Mutographs of Cancer: Gastric Organoids (2019-08-07)
Dataset
EGAD00001005234
-
RNA-seq analysis of megakaryocytes and granulocytes in Quebec platelet disorder
Study
EGAS00001001840
-
Genomic profiling of Acute Lymphoblastic Leukemia in Ataxia Telangiectasia patients reveals tight link between ATM mutations and chromothripsis
Study
EGAS00001002270
-
Women's Health Study Accelerometry Dataset
Study
phs001964
-
DSRCT RNA genomic sequencing
Study
EGAS00001002770
-
The Melbourne Urological Research Alliance (MURAL) Collection of Patient-Derived Models of Prostate Cancer
Study
phs003369
-
RaScALL: Rapid screening of RNA-seq in acute lymphoblastic leukaemia
Study
EGAS00001006460
-
Systematic kinase inhibitor profiling identifies CDK9 as a synthetic lethal target in NUT midline carcinoma
Study
EGAS00001002588
-
Complete Genomics paired end sequencing; Ovarian cancer
Study
EGAS00001000158
-
Whole-exome sequencing of ovarian clear cell carcinoma in clinical outliers
Study
EGAS00001004248
-
Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes
Study
EGAS00001006260
-
Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Study
EGAS00001001234
-
Blood RNA-seq from Mexican DMD patients and healthy controls
Study
EGAS00001004907
-
Natural History, Pathogenesis and Outcome of Melorheostosis
Study
phs001976
-
Exome Sequencing of Pleuropulmonary Blastoma
Study
phs000543
-
CAGEKID: Cancer Genomics of the Kidney
Study
EGAS00001000083
-
CAGEKID: Cancer Genomics of the Kidney - Targeted Sequencing
Study
EGAS00001007004
-
Single cell RNAseq of stenotic, inflamed and non-inflamed transmural lesions from patients with Crohn's disease
Dataset
EGAD50000000559
-
Amplified EPOR/JAK2 genes define a unique subtype of acute erythroid leukemia
Study
EGAS00001005810
-
TEST_STUDY for submitter testing
Study
EGAS00001000889
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
A Genome-Wide Association Study of Peripheral Arterial Disease
Study
phs000203
-
Human Pancreatic Islet RNAseq - Lund
Study
EGAS00001004042
-
Phenotyping data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004056
-
GWAS data on human pancreatic islets from 191 donors - Lund
Study
EGAS00001004044
-
scRNA-seq of total bone marrow mononuclear cells and CD3+ T cells of multiple myeloma patients and healthy donors
Study
EGAS00001006980
-
EstMB cohort participants sequenced with MGISEQ-2000 platform
Dataset
EGAD50000002213
-
A Comprehensive Platform for Analyzing Longitudinal Multi-Omics Data
Study
phs003203
-
Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age
Study
phs000596
-
The Multiethnic Cohort (MEC) Study
Study
phs002183
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
Field Studies of Human Immunity to Amebiasis in Bangladesh
Study
phs001476
-
2018_ETO_WGS
Study
EGAS00001002804
-
2015_AML_ETO
Study
EGAS00001002897
-
2015_AML_ETO_WGS_additional
Study
EGAS00001002898
-
MM samples for epigenomic translocation of H3K4me3 broad domains following super-enhancer hijacking
Study
EGAS00001005684
-
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Study
phs001339
-
RNU2-2 splicing signature RNA-Seq
Dataset
EGAD50000002045
-
Highly complex single-cell mixture of 5 individuals of low cell number
Dataset
EGAD50000000479
-
Synthetic genotypes and phenotypes of 500.000 individuals
Study
EGAS00001006552
-
Correlative Studies for Protocol #14-C-0059: T Cells Expressing an Anti-GD2 Chimeric Antigen Receptor in Patients with GD2+ Solid Tumors, a Collaboration with CIMAC-CIDC
Study
phs003455
-
Organ maturation in preparation for birth (Peds RFA) to develop a tissue resource and a single-cell atlas of organ development and maturation for dissemination among the scientific and clinical community: RNA (2025-10-14)
Dataset
EGAD00001015737
-
Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Ischemia (BEST CLI-BioLINCC)
Study
phs003844