-
CCDG CVD: VIRGO - Variation in Recover-Role of Gender on Outcomes of Young Acute Myocardial Infarction (AMI) Patients
Study
phs001259
-
Heart Failure Network Oral Iron Repletion Effects on Oxygen Uptake in Heart Failure (HFN IRONOUT-BioLINCC)
Study
phs003557
-
De Novo Mutation Rates at the Single-Mutation Resolution in the Human Genome
Study
phs002391
-
Genetic Testing to Understand and Address Renal Disease Disparities
Study
phs001620
-
Circulating Genomic Determinants of Treatment Failure in Hodgkin Lymphoma
Study
phs003435
-
University of Michigan Clinical Sequencing Exploratory Research (CSER)
Study
phs000673
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
Introducing Federated EGA Affiliates: a newly defined tier in the Federated EGA Network
Blog
fega-affiliates
-
Reference exome data for Australian Aboriginal populations to support health-based research
Study
EGAS00001003745
-
Infiltrative and drug-resistant slow-cycling cells support metabolic heterogeneity in glioblastoma
Study
EGAS00001003251
-
Bladder Cancer Organoids as a Functional System to Model Different Disease Stages and Therapy Response
Study
phs003149
-
NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate
Study
phs001359
-
Exome Sequencing to Identify Medically Relevant Associations in Finnish Sub-Isolate Samples from the FINRISK Cohort
Study
phs000756
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
Aspirin and Inflammation: Mutations, Genes, Pathways and Prevention in Barrett's Esophagus
Study
phs001654
-
A Population Genomics Study Using a Disease-Targeted Cell model: Integration of
Study
phs000225
-
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Ghana Prostate Study
Study
phs000838
-
AC-ICAM: An Atlas and Compass of Immune-CAncer-Microbiome Interactions in Colon Cancer
Study
phs002978
-
NINDS Deep Sequencing for the Detection of Viral Sequences in Primary Progressive Multiple Sclerosis Brains
Study
phs000715
-
Genomic Landscape of Multiple Myeloma and of its Precursor Conditions, and its Clinical Implications
Study
phs003846
-
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
-
Post_Mortem_Tissue_COVID19_RNA
Study
EGAS00001004442
-
Post_Mortem_Tissue_COVID19_spatial
Study
EGAS00001004441
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD - Imaging)
Study
phs003562
-
Women's Health Initiative Clinical Trial and Observational Study - Imaging
Study
phs003824
-
Single cell RNAseq data of human neurons, Bouwen et al Nat Comm 2025
Study
EGAS50000001369
-
Molecular characterization of NASH-HCC
Dataset
EGAD00001007524
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
ELLIPSE Prostate Cancer Meta-Analysis and Genotyping
Study
phs001120
-
Prevention and Early Treatment of Acute Lung Injury Network - Vitamin D to Improve Outcomes by Leveraging Early Treatment (PETAL VIOLET-BioLINCC)
Study
phs003879
-
Atezolizumab Plus Personalized Neoantigen Vaccination in Patients with Urothelial Cancer: a Phase 1 Trial
Study
phs003922
-
RNA-Seq in Patients with Primordial Dwarfism
Dataset
EGAD00001000640
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
North American Mitochondrial Disease Consortium Patient Registry and Biorepository
Study
phs001538
-
Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs002304
-
Randomized Evaluation of Sedation Titration for Respiratory Failure (RESTORE-BioLINCC)
Study
phs003783
-
The EGA Helpdesk team: 2025 in review and what we are building next
Blog
ega-helpdesk-team-2025-in-review-and-upcoming-improvements
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DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
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
Study
phs000439
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Coronary Artery Risk Development in Young Adults (CARDIA)
Study
phs000236
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
Heart Failure Network - Effectiveness of Ultrafiltration in Treating People with Acute Decompensated Heart Failure and Cardiorenal Syndrome (HFN CARRESS - BioLINCC)
Study
phs003510
-
Light at Night and Prostate Cancer in the Health Professionals Follow-Up Study
Study
phs003538
-
Parallel CRISPR Editing of Familial ALS Mutations
Study
phs002440
-
Highlights from 2025: Our top 10 requested studies
Blog
top-10-studies-2025
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
-
scRNAseq of colonic organoids derived from biopsies taken from healthy human individuals treated with IL22
Dataset
EGAD00001010168
-
NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Siblings with Ischemic Stroke Study, SWISS)
Study
phs000327
-
Implementation of the GDPR
Documentation
about/privacy-notice
-
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
Study
phs002324
-
Cryptococcosis in Previously Healthy Adults
Study
phs003871
-
Privacy Notice for Helpdesk service
Documentation
data-protection/privacy-notice/ega-helpdesk
-
National Cancer Institute (NCI) Genome Wide Association Study (GWAS) of Lung Cancer in Never Smokers
Study
phs000634
-
Characterization_of_individual_foci_of_multicentric_multifocal_breast_cancer_using_targeted_next_generation_sequencing
Study
EGAS00001000407
-
Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies
Study
phs000684
-
NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG)
Study
phs001608
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
Influence of Genomic Landscape on Cancer Immunotherapy for Newly Diagnosed Ovarian Cancer: Biomarker Analyses from the IMagyn050 Randomized Clinical Trial
Study
EGAS00001006838
-
ROCHE PD 92 Multiome dataset
Dataset
EGAD50000000964
-
Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
-
Genetic Heterogeneity of the familial gastric neuroendocrine tumors (2018-06-06)
Dataset
EGAD00001004153
-
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Study
phs002140
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
-
Population Architecture using Genomics and Epidemiology (PAGE)
Study
phs000356
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
Coagulation and Fibrinolysis in a Pediatric Insulin Titration Trial
Study
phs003016
-
Jackson Heart Study (JHS-BioLINCC)
Study
phs003740
-
Providing access to COVID-19 data: one year later
Blog
providing-access-to-covid-19
-
HBCC Postmortem Psychiatric Molecular Studies
Study
phs000979
-
Characterization of individual foci of multicentric/multifocal breast cancer using targeted next generation sequencing
Dataset
EGAD00001000624
-
National Human Genome Research Institute (NHGRI) Clinical Sequencing Exploratory Research (CSER) The MedSeq Project: Integration of Whole Genome Sequencing into Clinical Medicine (HG006500)
Study
phs000958
-
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Study
phs000574
-
Cell and Circuit-Specific Exploration of HIV Neurogenomics in Context of Opiate and Cocaine Misuse
Study
phs003080
-
Resuscitation Outcomes Consortium (ROC) Cardiac Epidemiologic Registry (Cardiac Epistry) Version 3 (ROC-Cardiac Epistry 3-BioLINCC)
Study
phs003726
-
Resuscitation Outcomes Consortium (ROC) Cardiac Epidemiologic Registry (Cardiac Epistry) Versions 1 and 2 (ROC-Cardiac Epistry 1 and 2-BioLINCC)
Study
phs003803
-
Mayo-Perlegen LEAPS (Linked Efforts to Accelerate Parkinson's Solutions) Collaboration
Study
phs000048
-
Genomic Characterization of Head and Neck Squamous Cell Carcinoma Cell Lines
Study
phs001581
-
National Institute of Arthritis and Musculoskeletal and Skin Diseases and Istanbul Faculty of Medicine Genome-wide Association Study of Behçet's Disease (Turkish)
Study
phs000272
-
Genetic Causes of Congenital Anosmia
Study
phs003328
-
Acute Respiratory Distress Network (ARDSNet) Studies 06 and 08 Prospective, Randomized, Multicenter Trial of Aerosolized Albuterol Versus Placebo for the Treatment of Acute Lung Injury (ALTA) (ARDSNet-ALTA-BioLINCC)
Study
phs003743
-
Study of Clinical Efficacy of Antimicrobial Therapy Strategy Using Pragmatic Design in Idiopathic Pulmonary Fibrosis (CleanUP IPF-BioLINCC)
Study
phs004314
-
The BC Cancer Agency's Personalized Onco-Genomics Project
Study
EGAS00001001159
-
Djerroudi et al., E-cadherin inactivation shapes tumor microenvironment specificities in invasive lobular carcinoma
Study
EGAS50000000761
-
METABRIC: Data from Pereira et al (2016), The somatic mutation profiles of 2433 breast cancers refine their genomic and transcriptomic landscapes. Nat Comms 7.
Study
EGAS00001001753
-
WES of adult intellectual disabilities with co-morbid psychiatric disorders (2019-08-07)
Dataset
EGAD00001005236
-
Hofer et al., A specific subpopulation of cancer-associated fibroblasts promotes resistance to chemotherapy in triple-negative breast cancer by upregulating G0S2 protein
Study
EGAS50000000886
-
First datasets available in the Federated EGA Network
Blog
first-datasets-available-in-Federated-EGA
-
Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Study
EGAS00001002678
-
The Genetic Architecture of Smoking and Smoking Cessation
Study
phs000404
-
ICGC Data Access Compliance Office
Dac
EGAC00001000010
-
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Study
phs001496
-
Adipose Tissue Omics In Obesity
Study
phs003390
-
Acute Respiratory Distress Network (ARDSNet) Studies 01 and 03 Lower Versus Higher Tidal Volume, Ketoconazole Treatment and Lisofylline Treatment (ARMA/KARMA/LARMA) (ARDSNet-ARMA/KARMA/LARMA-BioLINCC)
Study
phs003734
-
Targeted_sequencing_of_genes_recurrently_mutated_in_AML
Study
EGAS00001000408
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561