-
NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study
Study
phs000974
-
A comprehensive DNA methylation landscape of human and mouse cell lines derived from hematological malignancies
Study
EGAS50000000627
-
Finnish_population_cohort_genotyping_B
Study
EGAS00001001047
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
scRNA-seq data of human nuclei collected from the temporal cortex of 17 individuals.
Study
EGAS00001002882
-
Transcriptomic analysis of Acute Myeloid Leukemia stem cells
Study
EGAS00001004402
-
Whole genome sequencing in 1038 index cases reveals novel causative genes in pulmonary arterial hypertension
Dataset
EGAD00001003423
-
TSCA-LI amplicon sequencing of called variants in WXS data of DSALL.
Dataset
EGAD00001003275
-
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Study
phs001071
-
Michigan Polybrominated Biphenyl (PBB) Exposure Registry
Study
phs001862
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis
Study
phs001499
-
Esophageal Squamous Cell Carcinoma Precursor Study
Study
phs002814
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
-
Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency
Study
phs002990
-
Dilgom_Exome
Study
EGAS00001000086
-
Study of the rare and low frequency variants in the Saguenay-Lac-Saint-Jean population
Study
EGAS00001003103
-
C3 SNPs and outcome after lung transplantation
Study
EGAS00001003843
-
Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol
Study
EGAS00001002854
-
EGA FUSE Client
Documentation
access/download/visualisation/fuse-client
-
Genomic Origins and Admixture in Latinos (GOAL)
Study
phs000750
-
NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish
Study
phs000956
-
Chromothripsis in Patient WHIM-09
Study
phs000856
-
Exome Sequencing for Diseases of the Immune System: X-linked Immunodeficiency with Magnesium Defect, EBV Infection, and Neoplasia (XMEN)
Study
phs000365
-
Glial Cell Line-Derived Neurotrophic Factor (GDNF) Polymorphisms and Anxiety, Depression
Study
phs000713
-
MUSIC: Long-TerM OUtcomes after the Multisystem Inflammatory Syndrome In Children
Study
phs002770
-
Puerto Rico Heart Health Program (PRHHP-BioLINCC)
Study
phs003930
-
Analysis of CD20 loss in patients treated with Mosunetuzumab
Study
EGAS50000000151
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
Genetic diversity and continuity of the population of the UAE
Study
EGAS00001004362
-
Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
-
BCR Signaling in human BM PC
Study
EGAS00001004948
-
Exome sequencing from cfDNA blood samples. 159 samples at 2x101bp Illumina reads in Fastq format.
Study
EGAS00001006656
-
Copy numbers in resectable gastric cancer treated with surgery alone
Study
EGAS00001007394
-
Cardiovascular Health Study (CHS) Cohort: an NHLBI-funded observational study of risk factors for cardiovascular disease in adults 65 years or older
Study
phs000287
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Framingham Heart Study (FHS)
Study
phs002911
-
Copy number profiling of primary samples and cell lines of retinoblastoma
Study
EGAS00001001715
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
-
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
-
scRNAseq of colonic organoids derived from biopsies taken from healthy human individuals treated with IL22
Dataset
EGAD00001010168
-
Sickle Cell Disease Implementation Consortium Registry (SCDIC Registry-BioLINCC)
Study
phs004203
-
Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS00001007461
-
Cross-Sectional Characterization of Idiopathic Bronchiectasis
Study
phs001279
-
NSIGHT North Carolina Newborn Exome Sequencing for Universal Screening (NC NEXUS)
Study
phs002095
-
A Randomized, Double-Blind, Crossover Study of Sodium Phenylbutyrate (Buphenyl) and Low-Dose Arginine (100 mg/kg/day) Compared to High-Dose Arginine (500 mg/kg/day) Alone on Liver Function, Ureagenesis and Subsequent Nitric Oxide Production in Patients with Argininosuccinic Aciduria (ASA)
Study
phs001305
-
Foregut Microbiome in Development of Esophageal Adenocarcinoma
Study
phs000260
-
International Consortium to Identify Genes and Interactions Controlling Oral Clefts
Study
phs000094
-
CRCbiome: Gut metagenome of Norwegian screening participants using FIT sampling
Study
EGAS50000000170
-
Youth-GEMs, the project using data to define the mental health trajectories of young people
Blog
youth-gems-mental-health
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Dataset
EGAD00001000817
-
African American Multiple Myeloma GWAS
Study
phs001632
-
Starr County Health Studies' Genetics of Diabetes Study
Study
phs000143
-
High density copy number analysis and whole exome sequencing of unselected chronic lymphocytic leukemia cases and of paired chronic lymphocytic leukemia and Richter Syndrome cases
Study
phs000364
-
Genetic Analysis of Normal Human Facial Variation
Study
phs000949
-
A Genomic Atlas of Systemic Interindividual Epigenetic Variation in Humans (GTEx)
Study
phs001746
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in NEIGHBOR Samples
Study
phs000458
-
ADAGESIII: Contribution of genotype to glaucoma phenotype in African Americans
Study
phs001673
-
Framingham Heart Study-Cohort (FHS-Cohort) - Imaging
Study
phs003593
-
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
Gut microbiome dynamics unravelled with metagenomics sequencing
Blog
gut-microbiome-dynamics-unravelled
-
A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children with SCID Disorders
Study
phs001392
-
GECCO: Detecting Common and Rare Genetic Loci and GxE Interactions in Colorectal Cancer
Study
phs001315
-
Kids First: Genomic Etiologies of CHARGE Syndrome, Related Conditions and Structural Anomalies
Study
phs002592
-
Providing safe access to sensitive human data across borders: Federated EGA becomes a reality
Blog
safe-access-to-sensitive-human-data-federated-ega
-
Molecularly matched targeted therapies plus radiotherapy in patients with newly diagnosed glioblastoma without MGMT promoter hypermethylation (N2M2/NOA-20 phase I/IIa umbrella trial)
Study
EGAS00001008033
-
The last addition to the list of clonal evolution studies in the EGA
Blog
the-last-addition-to-the-list-of-clonal-evolution-studies-in-the-ega
-
Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing
Study
phs000876
-
Defining T cell States Associated with Response to Checkpoint Immunotherapy in Melanoma
Study
phs001680
-
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
-
Oncoarray Consortium - Lung Cancer Studies
Study
phs001273
-
NHLBI TOPMed: The Jackson Heart Study (JHS)
Study
phs000964
-
Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Study
phs001317
-
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis (FSGS)
Study
phs000777
-
The Institute for Genomic Medicine at Nationwide Children's Hospital Pediatric Cancer and Blood Disorder Project
Study
phs001820
-
Idiopathic Pulmonary Fibrosis Network (IPFNet) Sildenafil Trial of Exercise Performance in Idiopathic Pulmonary Fibrosis (IPFNet-STEP-IPF-BioLINCC)
Study
phs004085
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
A Retrospective and Cross-Sectional Analysis of Patients Treated for SCID Since January 1, 1968
Study
phs001326
-
California Pacific Medical Center Research Breast Health Cohort
Study
phs000395
-
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Study
phs000424
-
Framingham Cohort
Study
phs000007
-
Multiple Myeloma Genomic Study (MMGS)
Study
phs001323
-
Bogalusa Heart Study (BHS-BioLINCC)
Study
phs004173
-
Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide Sequencing
Study
phs001554
-
GEnomics and Transcriptomics of Human INsulinoma (GETHIN)
Study
phs001422
-
Regulatory and Effector T cells in Oral Immunotherapy for Food Allergy
Study
phs001897
-
EGA metadata schema
Documentation
submission/metadata/ega-schema
-
Upcycling and merging data to challenge the dogma and identify new therapeutic targets for Glioblastoma
Blog
upcycling-and-merging-data-to-challenge-glioblastoma
-
Demographically Diverse Substance Use Disorder Cohorts of Dr. Stanley H. Weiss
Study
phs002140
-
GAW16 Framingham and Simulated Data
Study
phs000128
-
Health and Retirement Study (HRS)
Study
phs000428
-
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Study
phs000847
-
Serrated Colorectal Cancer: An Emerging Disease Subtype
Study
phs002171
-
All you need to know about our new DAC Portal v2
Blog
new-dac-portal-v2
-
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Study
phs001011
-
Surgical Treatment for Ischemic Heart Failure (STICH-BioLINCC)
Study
phs003493