-
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Study
EGAS00001005110
-
ChIP-seq data of H3K4me3, H3K27ac and H3K27me3 on multiple human embryonic tissues.
Study
EGAS00001003163
-
Multiomics analyses of Parkinson's disease midbrains
Study
EGAS00001004966
-
Test dataset with ligh-weight files
Dataset
EGAD00001009826
-
Whole Exome Sequencing data of glioma from the Chinese Glioma Genome Atlas (CGGA) project
Dataset
EGAD00001006445
-
Exome sequencing of Congenital Heart Disease families Royal Brompton
Dataset
EGAD00001000797
-
Diseased_heart_analysis__RNA_Adult
Study
EGAS00001008302
-
Gut metagenome/FR 2002
Study
EGAS00001005038
-
Limited Association between HRR Gene Alterations and HRD in Molecular Tumor Board Cancer Samples: Who should be tested for HRD?
Study
EGAS00001008063
-
Analysis of Epigenomes and Genome Topology in Colorectal Cancer
Study
phs002288
-
Normal Pressure Hydrocephalus
Study
phs002296
-
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251
-
Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking
Study
EGAS00001004014
-
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Study
phs000424
-
EGA FUSE Client
Documentation
access/download/visualisation/fuse-client
-
GenomeEUtwin Data Access Committee
Dac
EGAC00000000007
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Pharmacokinetic Polymorphisms in Japanese General Population
Study
phs002985
-
This study generated Oxford Nanopore long read sequencing data of cancer cell line mixtures for validating long-read variant calls in cancer genomics
Study
EGAS00001008107
-
Gene Expression Signatures Characterized by Longitudinal Stability and Inter-Individual Variability Delineate Baseline Phenotypic Groups with Distinct Responses to Immune Stimulation
Study
phs001512
-
DEMENTIA-SEQ: WGS in Lewy Body Dementia and Frontotemporal Dementia
Study
phs001963
-
INCLUDE: Genetic Underpinnings of the Multifactorial Phenotype of Trisomy 21 Patients Unveiled by Multi-Omics Approaches
Study
phs002983
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency
Study
phs000776
-
Establishment of an iPSC Repository Derived from Healthy Volunteers
Study
phs003649
-
Assessment of candidate high-grade serous ovarian carcinoma predisposition genes through integrated germline and tumour sequencing
Study
EGAS50000000770
-
Plasma cell‐Free transcriptome profiling in chronic liver disease
Study
EGAS50000000545
-
Fragmentomics Uncover Non-Mutational HRD Features
Study
EGAS00001008190
-
Comprehensive pharmacogenomic characterization of gastric cancer
Study
EGAS00001004106
-
Three-dimensional human alveolar stem cell culture models reveal infection response to SARS-CoV-2
Study
EGAS00001004508
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - WGS data
Study
EGAS00001006610
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - Cancer Panel data
Study
EGAS00001006642
-
Human NXPE1 mediates variation in sialic acid O-acetylation in Colon Tissue
Study
EGAS00001007704
-
Recurrent intra-tumour heterogeneity is a hallmark of metastatic prostate cancer
Study
EGAS50000001312
-
First datasets available in the Federated EGA Network
Blog
first-datasets-available-in-Federated-EGA
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): Identification of VUR genes by exome sequencing
Study
phs000778
-
NHLBI TOPMed: Lung Tissue Research Consortium (LTRC)
Study
phs001662
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
Whole Exome Sequencing of One Nuclear Family with Non-syndromic Sensorineural Hearing Loss
Study
phs000969
-
NHLBI TOPMed: Genetics of Asthma in Latino Americans (GALA)
Study
phs001542
-
Single-cell/single-nucleus RNA-seq of Embryonal Tumor with Multilayered Rosettes (ETMR)
Study
EGAS50000000937
-
Whole genome sequencing data of pediatric hypodiploid acute lymphoblastic leukemia
Study
EGAS50000001305
-
Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
-
Small intestinal plasma cells transcriptome profiles
Study
EGAS00001003345
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
Targeted_sequencing_of_blood_DNA_from_Human_twins_
Study
EGAS00001002210
-
Molecular profiling of longitudinally observed small colorectal polyps: a cohort study
Study
EGAS00001003284
-
Control samples, breast cancer clinical samples and matched patient-derived tumour xenografts (PDTXs) to develop and test a computational approach to discriminate human and mouse sequences in PDTXs
Study
EGAS00001002445
-
Transcriptome analysis of endometrial organoids derived from patients with Mayer-Rokitansky-Küster-Hauser syndrome
Study
EGAS00001005908
-
ONGOING CHROMOSOMAL INSTABILITY ACROSS ANEUPLOID SUBTYPES OF CHILDHOOD B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA ASSOCIATES WITH DISEASE PROGRESSION
Dac
EGAC50000000005
-
Glioblastoma CRISPR Screen (2016-06-02)
Dataset
EGAD00001002158
-
Glioblastoma CRISPR Screen (2017-04-27)
Dataset
EGAD00001003308
-
Nanopore sequencing enables allelic phasing of FLG loss-of-function variants, intragenic copy number variation and methylation status in atopic dermatitis and ichthyosis vulgaris
Study
EGAS50000000166
-
Rare Cancer Tumors Project
Study
phs000725
-
Esophageal Squamous Cell Carcinoma Precursor Study
Study
phs002814
-
Microbiota 16S sequencing study in NSCLC patients eligible for surgery without neoadjuvant treatment
Study
EGAS00001004728
-
Blastic plasmacytoid dendritic cell neoplasm (BPDCN)_cases
Dataset
EGAD00010001727
-
10X 3' V2 data of single immune cells in hepatocellular carcinoma
Dataset
EGAD00001005961
-
ATAC-SEQ MAIN - PHASE 1
Dataset
EGAD00001001320
-
Pharmacogenomics of Mercaptopurine Intolerance in Children with Acute Lymphoblastic Leukemia (AALL03N1)
Study
phs002846
-
VitGene Generalized Vitiligo Genetics Study-Phase 2
Study
phs000224
-
ENU_LS_411N_TripleTherapy
Study
EGAS00001001777
-
Solve-RD Solving the Unsolved Rare Dieseases
Study
EGAS00001003851
-
Acquiring and sequencing of all 24 single human chromosomes
Study
EGAS00001003300
-
Policy Documentation
Documentation
access/data-access-committee/policy-documentation
-
Kids First and INCLUDE: Down Syndrome, Heart Defects, and Acute Lymphoblastic Leukemia
Study
phs002330
-
Norepinephrine Transporter Blockade as a Pathophysiological Biomarker in Neurogenic Orthostatic Hypotension
Study
phs001595
-
INSIGHT (Intervention Nurses Start Infants Growing on Healthy Trajectories) Cohort
Study
phs001498
-
Combination of ribociclib and gemcitabine for the treatment of medulloblastoma
Study
EGAS00001006001
-
National Institute on Aging (NIA) SardiNIA Study
Study
phs000338
-
ALCHEMIST Study
Study
phs001140
-
Data access committee for "Detection of brain cancer using genome-wide cell-free DNA fragmentomes"
Dac
EGAC50000000605
-
Bulk WES Fastq Files for 103 Samples of Cornell-NCI DLBCL Genomic Project
Dataset
EGAD50000001747
-
Germline Sequencing for Aggressive Prostate Carcinoma
Study
phs000661
-
Extracellular microRNA Biomarkers for Diagnostic and Prognostic Assessment of Preeclampsia at Triage
Study
phs003169
-
NCI's Collection of Studies for General Cancer Research
Study
phs003967
-
An atlas of transcribed enhancers across helper T cell diversity for decoding human diseases
Study
JGAS000689
-
Identification of genes involved in congenital disorders of glycosylation and 3-methylglutaconic aciduria (2018-03-14)
Dataset
EGAD00001004038
-
Genome-Wide Analysis for Addiction Susceptibility Genes
Study
phs001266
-
Gabriella Miller Kids First Pediatric Research Program for Infantile Hemangiomas Associated with Multi-Organ Structural Birth Defects
Study
phs001785
-
Center for Common Disease Genomics [CCDG] Neuropsychiatric: Autism Spectrum Disorder (ASD) – Whole Exomes
Study
phs002502
-
dbGaP Collection: NHLBI Heart Failure Related dbGaP Data (No IRB requirement)
Study
phs001991
-
Genome Variation among HIV-Resistant People with Hemophilia
Study
phs000445
-
Genetics of Human Developmental Brain Disorders
Study
phs000492
-
Microbiome-Host Interactions in Oral Squamous Cell Carcinoma: a Metatranscriptomic Exploratory Study
Study
phs002678
-
InTEAM Consortium - Alcoholic Hepatitis
Study
phs001807
-
Examination of Engineered LINE-1 Integration Events in HeLa Cells
Study
phs001669
-
Diverse_outcomes_of_controlled_human_malaria_infection_originate_from_host_intrinsic_immune_variation_and_not_var_gene_switching
Study
EGAS00001003766
-
RNA-Seq of vocal fold fibroblasts in Reinke’s edema and control subjects
Study
EGAS00001005130
-
Genomic Studies of Bipolar Disorder in a Large Cohort from The Netherlands
Study
phs002856
-
MUSIC: Long-TerM OUtcomes after the Multisystem Inflammatory Syndrome In Children
Study
phs002770
-
GAW16 Framingham and Simulated Data
Study
phs000128
-
Predicting brain tumor recurrence: development and validation of a DNA-methylation based nomogram in meningioma
Study
EGAS00001003490
-
CONNECTS Master Protocol for Clinical Trials targeting Macro- and Micro-Immuno-Thrombosis, Vascular Hyperinflammation, and Hypercoagulability and Renin-Angiotensin-Aldosterone System (RAAS) in Hospitalized Patients with COVID-19 (ACTIV-4 Host Tissue)
Study
phs003708
-
Study of Addiction: Genetics and Environment (SAGE)
Study
phs000092
-
PAX4 loss of function increases diabetes risk by altering human pancreatic endocrine cell development
Dataset
EGAD50000000516
-
How are we funded?
Documentation
about/projects-and-funders/funders
-
National Institute of Neurological Disorders and Stroke (NINDS), Family Study of Essential Tremor (FASET), Identification of Susceptibility Genes for Essential Tremor
Study
phs000966
-
Neurodevelopmental Genomics: Trajectories of Complex Phenotypes
Study
phs000607
-
Team
Documentation
about/team
-
A microRNA-signature that correlates with cognition and is a target against cognitive decline
Study
EGAS00001005627