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Shank2 Gene knockout/modified WGS data
Dataset
EGAD00001004575
-
TCELL PILOT ATAC-SEQ
Dataset
EGAD00001001317
-
Chondromyxoid fibroma
Dataset
EGAD00001001063
-
Single-cell colony targeted DNAseq
Dataset
EGAD00001010193
-
Exome sequencing of Congenital Heart Disease families Toronto
Dataset
EGAD00001000799
-
INCLUDE: The Epidemiology of Transient Leukemia in Newborns with Down Syndrome
Study
phs002982
-
Varieties of Impulsivity in Opiate and Stimulant Users
Study
phs001647
-
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
-
Weighing Risks and Benefits of Laparoscopic Anti-Reflux Surgery in Patients With Idiopathic Pulmonary Fibrosis (WRAP-IPF-BioLINCC)
Study
phs003968
-
Idiopathic Pulmonary Fibrosis Network (IPFNet) Sildenafil Trial of Exercise Performance in Idiopathic Pulmonary Fibrosis (IPFNet-STEP-IPF-BioLINCC)
Study
phs004085
-
Privacy Notice for Data Access Committee Account
Documentation
data-protection/privacy-notice/ega-dac
-
Characterization of individual foci of multicentric/multifocal breast cancer using targeted next generation sequencing
Dataset
EGAD00001000624
-
Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs
Study
JGAS000057
-
First datasets available in the Federated EGA Network
Blog
first-datasets-available-in-Federated-EGA
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Exome sequencing in HIV+ Viremic Non-Progressors (VNPs) and HIV+ Progressors
Dataset
EGAD50000000111
-
Childhood arthritis DNA (2020-01-15)
Dataset
EGAD00001005785
-
WGS of Biobank iPSC lines
Dataset
EGAD00001008769
-
Whole exome sequencing of a sinonasal glomangiopericytoma case
Dataset
EGAD00001008291
-
Phylogenetic development of childhood tumours
Dataset
EGAD00001005770
-
EGA synthetic data
Documentation
synthetic-data
-
Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection
Dataset
EGAD00001006259
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Genetics of Atrial Fibrillation
Study
phs002811
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Pharmacokinetic Polymorphisms in Japanese General Population
Study
phs002985
-
NHLBI TOPMed - NHGRI CCDG: The Johns Hopkins University School of Medicine Atrial Fibrillation Genetics Study
Study
phs001598
-
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
-
A Genomic Atlas of Systemic Interindividual Epigenetic Variation in Humans (GTEx)
Study
phs001746
-
The Lung Genomics Research Consortium (LGRC)
Study
phs000624
-
Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease
Study
phs001591
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
All you need to know about our new DAC Portal v2
Blog
new-dac-portal-v2
-
Virtual Growing Child 5-Dimensional Functional Models for Treating Respiratory Anomalies (dMRI-VGC)
Study
phs004002
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Tissue Biopsy Study
Study
phs001048
-
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Study
phs001339
-
Rare Disease Susceptibility Variant Study in Children with Crohn's Disease and Their Parents Using Targeted Gene Sequencing.
Study
phs001751
-
Nicotine dependence GWAS meta-analysis across European and African American ancestries
Study
phs001532
-
Genetic Basis of Breast Cancer Resistance in BRCA1 Mutation Carrier
Study
phs001243
-
NIH Roadmap Epigenomics Program - Broad Institute
Study
phs000700
-
Genomic Data Archive From the Network for Pancreatic Organ Donors With Diabetes
Study
phs002861
-
Human Pilocytic Astrocytoma Single Cell RNA Sequencing
Study
phs001854
-
VA APOLLO Project - Research for Precision Oncology (RePOP)
Study
phs001374
-
Pharmacogenomic Interactions in Glioblastoma Cell Line Models
Study
phs001793
-
Genetic Epidemiology of Ovarian Cancer Histotypes
Study
phs003140
-
A Genome-Wide Association Study on Cataract and HDL in the Personalized Medicine Research Project Cohort
Study
phs000170
-
Pediatric Investigation of Genetic Factors Linked with Renal Progression (PediGFR): Chronic Kidney Disease in Children Cohort (CKiD)
Study
phs000650
-
Mapping Disease Pathways for Biliary Atresia
Study
phs003458