-
Foundation Medicine Adult Cancer Clinical Dataset (FM-AD)
Study
phs001179
-
H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa
Study
EGAS00001007250
-
Successful Clinical Response in Pneumonia Therapy (SCRIPT)
Study
phs002300
-
Framingham Heart Study-Cohort (FHS-Cohort) - Imaging
Study
phs003593
-
Genome Diversity in Africa Project: Benin (2021-02-16)
Dataset
EGAD00001006970
-
Introducing Federated EGA Affiliates: a newly defined tier in the Federated EGA Network
Blog
fega-affiliates
-
CTN - 0051: Extended-Release Naltrexone vs. Buprenorphine for Opioid Treatment (X:BOT)
Study
phs002876
-
Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria
Study
phs000378
-
Data Use Ontology (DUO) at EGA
Blog
data-use-ontology
-
MP2PRT: Evaluation of an Inflammation Polygenic Risk Score (iPRS) to Predict Cancer Related Cognitive Impairment and Fatigue in Patients Receiving Chemotherapy for Non-Metastatic Breast Cancer in URCC0701 and URCC10055
Study
phs003688
-
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
-
Inflammatory Bowel Disease Exome Sequencing Study
Study
phs001076
-
Genomic Advances in Sepsis (GAinS): RNA-seq
Dataset
EGAD00001008730
-
Shedding light over COVID-19 susceptibility and severity
Blog
covid-19-susceptibility-and-severity
-
Foregut Microbiome and Risk of Gastric Intestinal Metaplasia, and Gastric Cancer Risk
Study
phs002566
-
A Genome-Wide Association Study of Peripheral Arterial Disease
Study
phs000203
-
TOPDECC-Trans-omics for Precision Dentistry and Early Childhood Caries: Genome-Wide Genotyping (CIDR) and Microbiome in the ZOE 2.0 Study
Study
phs002232
-
National Institute of Dental and Craniofacial Research (NIDCR) Sjögren's International Collaborative Clinical Alliance (SICCA): Center for Inherited Disease Research (CIDR) Genome-Wide Genotyping
Study
phs000672
-
National Sleep Research Resource (NSRR): Cleveland Family Study (CFS)
Study
phs002715
-
NIH RECOVER: A Multi-Site Observational Study of Post-Acute Sequelae of SARS-CoV-2 Infection in Adults
Study
phs003463
-
The Human Virome in Children and its Relationship to Febrile Illness
Study
phs000264
-
National Epidemiologic Survey on Alcohol and Related Conditions-III (NESARC-III)
Study
phs001590
-
NIH RECOVER-Pediatric: Understanding the Long-Term Impact of COVID on Children and Families
Study
phs003461
-
Jackson Heart Study (JHS-BioLINCC)
Study
phs003740
-
Genome-Wide Association Study of Celiac Disease
Study
phs000274
-
INCLUDE: The Epidemiology of Transient Leukemia in Newborns with Down Syndrome
Study
phs002982
-
REDS-IV-P Epidemiology, Surveillance and Preparedness of the Novel SARS-CoV-2 Epidemic (RESPONSE)
Study
phs003578
-
Projects
Documentation
about/projects-and-funders/projects
-
Jackson Heart Study (JHS) Cohort
Study
phs000286
-
Bibliography Statistics
Documentation
about/statistics/bibliography
-
Add Health: Longitudinal Study of a Nationally Representative Sample of Adolescents in Grades 7-12 in the United States during the 1994-95 School Year, Followed into Adulthood with Five Interviews/Surveys in 1995, 1996, 2001-02, 2008, and 2016-18
Study
phs001367
-
eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel
Study
phs001616
-
Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): COVID-19 Testing and Vaccination Social Network Diffusion for Diverse Criminal Legal Involved Communities
Study
phs003234
-
ACTIV-6: COVID-19 Outpatient Randomized Trial to Evaluate Efficacy of Repurposed Medications
Study
phs003941
-
Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-BioLINCC)
Study
phs004021
-
Childhood Cancer Survivor Study (CCSS)
Study
phs001327
-
Study on the Genetics of Alcoholism (COGA): African American Family GWAS
Study
phs000976
-
CRU-Ukrainian National Research Center for Radiation Medicine Trio Study
Study
phs001163
-
Federated discovery and sharing of genomic data using Beacons
Blog
federated-discovery-using-beacons
-
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
-
The Collaborative Study on the Genetics of Alcoholism (COGA)
Study
phs000763
-
Single Cell Analysis Program - Transcriptome (SCAP-T)
Study
phs000833
-
How upcycled prostate cancer sequences enabled key findings on telomeres length
Blog
prostate-cancer-sequences-enabled-key-findings-on-telomeres-length
-
The African American Breast Cancer Epidemiology and Risk (AMBER) Consortium Study
Study
phs000669
-
Study of Addiction: Genetics and Environment (SAGE)
Study
phs000092
-
Data Quality Control
Documentation
access/request-data/quality-control-reports
-
CIDR: Collaborative Study on the Genetics of Alcoholism Case Control Study
Study
phs000125
-
Research Program on Genes, Environment and Health (RPGEH)
Study
phs000788
-
A Genome-Wide Association Study of Heroin Dependence
Study
phs000277
-
eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants
Study
phs001584
-
The Genetic Architecture of Smoking and Smoking Cessation
Study
phs000404
-
eMERGE Network Study of the Genetic Determinants of Resistant Hypertension
Study
phs000297
-
Osteoporotic Fractures in Men (MrOS)
Study
phs000373
-
GA4GH
Documentation
about/projects-and-funders/ga4gh
-
eMERGE Network Genome-Wide Association Study of Red Cell Indices, White Blood Count (WBC) Differential, Diabetic Retinopathy, Height, Serum Lipid Levels, Specifically Total Cholesterol, HDL (High Density Lipoprotein), LDL (Low Density Lipoprotein), and Triglycerides, and Autoimmune Hypothyroidism.
Study
phs000360
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
Framingham Cohort
Study
phs000007
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
California Pacific Medical Center Research Breast Health Cohort
Study
phs000395
-
Federated EGA
Documentation
about/projects-and-funders/federated-ega
-
Multi-Ethnic Study of Atherosclerosis (MESA) Cohort
Study
phs000209
-
FEGA and European GDI: working together to improve human health
Blog
fega-and-gdi
-
Data Use Ontology (DUO)
Documentation
access/data-access-committee/data-use-ontology
-
Genome-Wide Association Study of Patients with Coccidioidomycosis
Study
phs002170
-
Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide Sequencing
Study
phs001554
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
OncoArray: Prostate Cancer
Study
phs001391
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
Identification of Genes Involved in Familial Coronary Artery Disease
Study
phs000514
-
Exome Sequencing Reveals Frequent Inactivating Mutations in BAP1, ARID1A, and PBRM1 in Intrahepatic Cholangiocarcinomas
Study
EGAS00001001108
-
Characterization of Sex Differences in Human Placentas
Study
phs002240
-
Establishment of xenogfafts and cultured cell lines from clinical samples
Study
JGAS000585
-
Screening Cases of Isolated Dystonia for Variants in CIZ1
Study
phs001455
-
RNA-Seq studies of Gene Expression in Cells and Networks in FI and ACC in Autism
Study
phs000609
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (mouse)
Study
EGAS00001004696
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (Human)
Study
EGAS00001004897
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1).
Study
EGAS00001006926
-
Nasal Polyp RNAsequencing, Skaraborg Sweden
Study
EGAS00001007088
-
Whole Exome Sequencing Study of TGFΒ Pathway Genes in HCV Liver Fibrosis
Study
phs001902
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19
Study
EGAS00001006372
-
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors
Study
EGAS00001000906
-
Gene Expression between PMD and Control LCLs at Baseline, E2, and E2 Withdrawal
Study
phs003003
-
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
Study
EGAS50000000298
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
An instructive role for IL7RA in the development of human B-cell precursor leukemia
Study
EGAS00001005347
-
Systematic identification of long non-coding RNAs potentially involved in gastrointestinal carncer
Study
JGAS000011
-
ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer
Study
EGAS00001003213
-
Efficacy of CDK4/6i in preclinical models of malignant pleural mesothelioma
Study
EGAS00001005352
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Mediators of Atherosclerosis in South Asians Living in America Study (MASALA)
Study
phs002980
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Whole Genome Sequencing to Discover Familial Myeloma Risk Genes
Study
phs001819
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Study
EGAS00001003719
-
Tumor Mutation Burden, Expressed Neoantigen and Immune Microenvironment in Diffuse Gliomas
Study
phs002653