-
A study of resistance to novel coronavirus infection in health care workers
Study
JGAS000562
-
Whole Genome sequencing of Angolan and Mozambican individuals
Study
EGAS00001007458
-
Exome-wide mutation analysis of cell-free DNA to simultaneously monitor the full spectrum of cancer treatment outcomes
Study
EGAS00001005906
-
Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies
Study
phs001672
-
NHLBI TOPMed: Partners HealthCare Biobank
Study
phs001024
-
NHLBI TOPMed - NHGRI CCDG: Intermountain INSPIRE Registry
Study
phs001545
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Study
EGAS00001004364
-
Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer
Study
EGAS50000000297
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
eMERGE Phase III Clinical Center at Partners HealthCare
Study
phs000944
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
-
Million Veteran Program (MVP) Summary Results from Non-Sensitive Omics Studies
Study
phs002453
-
EXCEED Study
Study
EGAS00001003499
-
Emirati Phased Diploid Trio-Assemblies
Study
EGAS50000001234
-
Normative Aging Study (NAS)
Study
phs000853
-
Single-cell analysis of upper airway cells reveals host-viral dynamics in influenza infected adults
Study
phs002039
-
ABHD11 Autoimmunity Study DAC
Dac
EGAC50000000750
-
Genetic Markers of Caries Risk in Diverse Underserved Children: CIDR
Study
phs003280
-
The Federated EGA network
Blog
the-federated-ega-network
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
CSER: Evaluating Utility and Improving Implementation of Genomic Sequencing for Pediatric Cancer Patients in the Diverse Population and Healthcare Settings of Texas: The KidsCanSeq Study
Study
phs002378
-
Noninvasive prenatal molecular karyotyping from maternal plasma
Study
EGAS00001000439
-
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): COVID-19 Experience Study (C19EX) Survey
Study
phs002537
-
IGNITE: Implementing GeNomics In practice: Genomic Medicine Implementation - The Personalized Medicine Program
Study
phs001978
-
Synthetic data - Genome in a Bottle
Study
EGAS00001005591
-
eMERGE III: Columbia GENIE (Genomic Integration with EHR)
Study
phs000961
-
CSER: Incorporating Genomics into the Clinical Care of Diverse NYC Children (NYCKidSeq)
Study
phs002337
-
A Study of the Genetic Causes of Complex Pediatric Disorders
Study
phs000490
-
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Study
phs001972
-
CSER: Exome Sequencing in Diverse Populations in Colorado and Oregon/CHARM Cancer Health Assessments Reaching Many
Study
phs002111
-
H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
-
Count Me In (CMI): The Metastatic Prostate Cancer (MPC) Project (CMI-MPCproject)
Study
phs001939
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases.
Study
EGAS00001003780
-
Characterization of Structural Variants in Acute Myeloid Leukemia Patients
Study
phs001847
-
NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)
Study
phs001466
-
Whole blood RNA-sequencing of covid-19 patients and healthy controls
Dataset
EGAD00001007776
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females
Study
phs002043
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD)
Study
phs002509
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Study
phs001894
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Simons Searchlight
Study
phs002512
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
Study
phs002042
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE)
Study
phs001740
-
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Study
phs002004
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange
Study
phs001766
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC)
Study
phs001741
-
GCAT | Genomes for life
Blog
gcat-genomes-for-life
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Autism - Simons Simplex Collection (SSC)
Study
phs001676
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: SPARK Simons Foundation Powering Autism Research for Knowledge
Study
phs002511
-
Count Me In (CMI): The Angiosarcoma (ASC) Project (CMI-ASCproject)
Study
phs001931
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder
Study
phs002044
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases
Dataset
EGAD00001005197
-
A transcriptomic approach to understand patient susceptibility to pneumonia after abdominal surgery
Study
EGAS00001007229
-
eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel
Study
phs001616
-
Resuscitation Outcomes Consortium (ROC) Controlled Study of the Clinical Effectiveness of Automated Real-Time Feedback on CPR Process Conducted at a Subset of ROC Sites (CPR) (ROC-CPR-BioLINCC)
Study
phs003818
-
Ex vivo RNA-seq in moderate COVID-19 monocytes
Dataset
EGAD00001009800
-
Global Microbiome Conservancy Sequence Data
Study
phs002235
-
Polycystic Ovary Syndrome (PCOS) Genetics
Study
phs000368
-
H3K27ac ChIP-seq in a selected group of AML patients
Dataset
EGAD00001007582
-
Sickle Cell Disease Implementation Consortium Registry (SCDIC Registry-BioLINCC)
Study
phs004203
-
Development and Validation of a Disability Severity Index for Charcot-Marie-Tooth Disease (CMT)
Study
phs001295
-
Northwestern NUgene Project: Type 2 Diabetes
Study
phs000237
-
CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen)
Study
phs000927
-
University of Utah Pelvic Organ Prolapse Disorder Study
Study
phs001439
-
NHLBI GO-ESP: Early-Onset Myocardial Infarction Exome Chip (Broad EOMI)
Study
phs000936
-
Introducing Federated EGA Affiliates: a newly defined tier in the Federated EGA Network
Blog
fega-affiliates
-
NSIGHT BabySeq Project
Study
phs002093
-
Prevention and Early Treatment of Acute Lung Injury (PETAL) - Low Tidal Volume Universal Support Feasibility of Recruitment for Interventional Trial (LOTUS FRUIT) (PETAL-LOTUS FRUIT-BioLINCC)
Study
phs003791
-
eIMPACT Trial: Modernized Collaborative Care to Reduce the Excess CVD Risk of Older Depressed Patients
Study
phs003283
-
Sickle Cell Disease Natural History Data Resource (SCD NHDR)
Study
phs003529
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
ACTIV-6: COVID-19 Outpatient Randomized Trial to Evaluate Efficacy of Repurposed Medications
Study
phs003941
-
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Study
phs001496
-
Adipose Tissue Omics In Obesity
Study
phs003390
-
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
-
FEGA and European GDI: working together to improve human health
Blog
fega-and-gdi
-
Breast Cancer in Blacks: Impact of Genomics, Healthcare Use and Lifestyle on Outcomes (BRIGHT)
Study
phs003466
-
Projects
Documentation
about/projects-and-funders/projects
-
Genome-Wide Association Study of Hypertriglyceridemia in Mexicans
Study
phs000618
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes
Study
phs000774
-
Highlights from 2025: Our top 10 requested studies
Blog
top-10-studies-2025
-
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
-
Implementation, Adoption, and Utility of Family History in Diverse Care Settings
Study
phs001641
-
About
Documentation
about/ega
-
Providing safe access to sensitive human data across borders: Federated EGA becomes a reality
Blog
safe-access-to-sensitive-human-data-federated-ega
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Federated EGA
Documentation
about/projects-and-funders/federated-ega
-
Providing access to COVID-19 data: one year later
Blog
providing-access-to-covid-19
-
GAW16 Framingham and Simulated Data
Study
phs000128
-
eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants
Study
phs001584
-
Development and Use of Network Infrastructure for High-Throughput GWA Studies
Study
phs000234
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888