-
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
-
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
-
The Somatic Mutational Landscape of Thyroid Cancer in Patients with Germline PTEN Mutations
Study
phs003640
-
Ischemia Reperfusion Responses in Human Lung Transplants at the Single Cell Resolution
Study
EGAS50000000490
-
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
-
Prediction of homologous recombination deficiency identifies colorectal tumors sensitive to PARP inhibition
Study
EGAS50000000426
-
Distinct immune cell infiltration patterns in PDAC exhibit divergent immune cell selection and immunosuppressive mechanisms
Study
EGAS50000000726
-
Mind Body Study: A Sub-Study on Psychosocial Factors and Microbiomes of Nurses in the Nurse's Health Study II
Study
phs003786
-
The genomic basis of childhood T-lineage acute lymphoblastic leukemia
Study
EGAS50000000016
-
Omic Studies in Children's Respiratory and Environmental Workgroup (CREW) Cohorts
Study
phs004036
-
TDP43 proteinopathy leads to divergent cryptic splicing in the cortex and spinal cord
Study
EGAS50000000575
-
Kids First: The Genomic Architecture of Hirschsprung Disease (HSCR)
Study
phs003662
-
Pipeline Olympics: Continuous benchmarking of computational workflows for DNA methylation sequencing data
Study
EGAS50000000541
-
Error-corrected flow-based sequencing at whole genome scale and its application to circulating cell-free DNA profiling
Study
EGAS50000000844
-
A Therapeutic Vaccine for Fibrolamellar Hepatocellular Carcinoma
Study
phs003970
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
FLT3-targeting and places FLT3 as an ideal therapeutic target to selectively eradicate LSCs, while sparing HSC.
Study
EGAS50000000437
-
Whole-genome methylation profiling of menstrual stem cells identifies novel biomarkers for endometriosis
Study
EGAS50000001640
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
Field_effect_of_healthy_and_diseased_livers_WGS
Study
EGAS00001002413
-
SINGLE_CELL_ANALYSIS_OF_IN_VITRO_ERYTHROPOIESIS
Study
EGAS00001000764
-
An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
-
Defective T-cell expansion in RASGRP1 deficiency
Study
EGAS00001002753
-
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Identification of rare germline variants in familial multiple myeloma
Study
EGAS00001004734
-
Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Study
EGAS00001004791
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001002602
-
Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer
Study
EGAS00001003791
-
Molecular_risk_stratification_in_patients_with_T1_colorectal_cancer_WES
Study
EGAS00001005734
-
Heat selection enables highly scalable methylome profiling in cell-free DNA for noninvasive monitoring of cancer patients
Study
EGAS00001006198
-
MGP Panel: a comprehensive targeted genomics panel for molecular profiling of multiple myeloma patients
Study
EGAS00001006222
-
Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes
Study
EGAS00001006260
-
Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers
Study
EGAS00001003556
-
Genomic_characterisation_of_MGUS__
Study
EGAS00001004124
-
Case Report: Rare IKZF1 gene fusions identified in neonate with congenital KMT2A-rearranged Acute Lymphoblastic Leukemia
Study
EGAS00001006947
-
Gut microbiome dynamics unravelled with metagenomics sequencing
Blog
gut-microbiome-dynamics-unravelled
-
Thymic epithelial transplantation for complete DiGeorge syndrome: RNA (2025-07-22)
Dataset
EGAD00001015648
-
Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
-
Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
-
RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors
Study
EGAS00001005588
-
An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington’s disease patient neurons
Study
EGAS00001006289
-
Clean sequence of LUAD in young never-smoker
Dataset
EGAD00001003890
-
WGS of human colorectal cancer organoid exposed to genotoxic pks+ E. coli
Dataset
EGAD50000000304
-
A neoadjuvant, phase II trial demonstrates efficacy and tolerability of Talimogene laherparepvec in cutaneous basal cell carcinoma (NeoBCC trial)
Dataset
EGAD50000000371
-
DupiAERD
Dataset
EGAD50000000565
-
Adipose tissue macrophage dysfunction is associated with a breach of vascular integrity in NASH
Dataset
EGAD50000000615
-
BAM files from whole-exome sequencing of 5 agressive B-cell lymphoma tumour samples
Dataset
EGAD50000000803
-
Moroccan Genome Project: Sequencing Data from 109 Whole Genomes of Moroccan Individuals
Dac
EGAC50000000353