-
Common origin and somatic mutation patterns of composite lymphomas and leukemias
Study
EGAS50000001017
-
Kids First: Genetics of Pediatric Germ Cell Tumors
Study
phs002322
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
Heart Failure: A Controlled Trial Investigating Outcomes of Exercise Training (HF-ACTION-BioLINCC)
Study
phs003599
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
WES of adult intellectual disabilities with co-morbid psychiatric disorders (2019-08-07)
Dataset
EGAD00001005236
-
Exome sequencing demonstrates a dual origin of relapses in retinoic-acid resistant acute promyelocytic leukemia.
Study
EGAS00001002893
-
Functional and genomic heterogeneity of long-term self-renewing compartment as the origin of treatment resistance in pancreatic tumors
Study
EGAS00001003442
-
Impact of Respiratory Virus Infections and Bacterial Microbiome Shifts on Lymphocyte and Respiratory Function in Infants Born Prematurely or Full Term
Study
phs001347
-
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
What is a DAC?
Documentation
access/data-access-committee/what-is-dac
-
EGA metadata schema
Documentation
submission/metadata/ega-schema
-
New England-Based Case-Control Study of Ovarian Cancer
Study
phs001034
-
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Study
phs001687
-
FIGHT-207: Anonymized Genomic Alterations and Clinical Responses
Study
phs003590
-
Single cell sequencing reveals the origin and the order of mutation acquisition in T-cell acute lymphoblastic leukemia.
Study
EGAS00001002830
-
Characterization_of_individual_foci_of_multicentric_multifocal_breast_cancer_using_targeted_next_generation_sequencing
Study
EGAS00001000407
-
A Genome-Wide Association Study of Heroin Dependence
Study
phs000277
-
Distribution of data using Live Distribution
Documentation
access/download/files/live-outbox
-
NHLBI TOPMed: MESA and MESA Family AA-CAC
Study
phs001416
-
University of Miami Study on Genetics of Autism and Related Disorders (AutismDisorders)
Study
phs000436
-
Studying Glioblastoma in a Human Organoid Tumor Transplantation Model
Study
phs003936
-
Characterization of individual foci of multicentric/multifocal breast cancer using targeted next generation sequencing
Dataset
EGAD00001000624
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719
-
All you need to know about our new DAC Portal v2
Blog
new-dac-portal-v2
-
Submission FAQ
Documentation
submission/metadata/submission/FAQ
-
Irish Covid19 WGS Alignment Data
Dataset
EGAD00001010098
-
NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai
Study
phs001644
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes
Study
phs000774
-
Federated EGA
Documentation
about/projects-and-funders/federated-ega
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Data Use Ontology (DUO)
Documentation
access/data-access-committee/data-use-ontology
-
Oncoarray Consortium - Lung Cancer Studies
Study
phs001273
-
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Study
phs001011
-
Multi-Ethnic Study of Atherosclerosis (MESA) Cohort
Study
phs000209
-
Privacy Notice for EGA Web user
Documentation
data-protection/privacy-notice/ega-website
-
Irish Covid19 WGS Raw Reads
Dataset
EGAD00001010186
-
Programmatic submission based on XML
Documentation
submission/metadata/submission/programmatic-submission-xml
-
Women's Health Initiative Clinical Trial and Observational Study - Imaging
Study
phs003824
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants
Study
phs001584
-
HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study
Study
phs002225
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415