-
Datasets of RNA-seq of tumor samples from clear cell renal cell carcinoma patients included in the Translational Program of the NIVOREN GETUG-AFU-26 trial
Dataset
EGAD50000001541
-
Wilm's tumor sequencing data
Dataset
EGAD00001011111
-
Genome-Wide Assessment of DNA Methylation in Systemic Lupus Erythematosus-Related Autoantibodies
Study
phs000947
-
ICR Exome Optimization series
Dataset
EGAD00001001462
-
CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
-
HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study
Study
phs002225
-
PHRT study of longitudinal sampling in ovarian cancer
Study
EGAS50000001424
-
dbGaP Collection: Open Translational Science in Schizophrenia (OPTICS)
Study
phs000887
-
Impact of Mutated CTCF DNA binding sites of Topologically associating domains on nearby Cancer Gene Regulation: A Multi-Omics Analysis
Study
EGAS50000001686
-
Small cell number RNA-seq (400 cells per sample)
Dataset
EGAD50000001830
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Genetic Epidemiology of COPD Study (COPDGene)
Study
phs002910
-
Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma.
Dataset
EGAD00001004795
-
Mutation analysis of 17 genes in plasma DNA of CRC patients using the AVENIO ctDNA Targeted Kit
Dataset
EGAD00001006103
-
Single cell RNA sequencing of colorectal cancer patients (KUL5)
Dataset
EGAD00001008585
-
The Pioneer 100 Wellness Project (P100)
Study
phs001363
-
A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma
Dataset
EGAD00001006190
-
Genetic Markers of Caries Risk in Diverse Underserved Children: CIDR
Study
phs003280
-
Clinical Outcomes for 344 Diffuse Large B-Cell Lymphoma Patients
Dataset
EGAD50000001536
-
STARR-seq of ERa binding sites in MCF7 and Ishikawa cell lines
Dataset
EGAD50000000015
-
Longitudinal snRNAseq and DNAseq of IDHmutant glioma
Dac
EGAC50000000973
-
Genetic Epidemiology of Chronic Lymphocytic Leukemia
Study
phs001568
-
Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
-
Paroxysmal_Neurological_Disorders_2
Study
EGAS00001000190
-
Paroxysmal_neurological_Disorders
Study
EGAS00001000386
-
Paroxysmal neurological disorders
Study
EGAS00001000048
-
Somatic L1 Retrotransposition in Colorectal Tumors
Study
phs000536
-
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Study
EGAS00001004940
-
BLUEPRINT: RNA-seq of progenitor cells
Dataset
EGAD00001000745
-
Cancerous Adaptive Dosing Melanoma WGS Dataset
Dataset
EGAD00001010926
-
Genetics of Glucose Regulation in Gestation and Growth (Gen3G) Cohort - Placenta Transcriptomics RNA Sequencing
Study
phs003151
-
10X 3' V2 data of single immune cells in hepatocellular carcinoma
Dataset
EGAD00001005961
-
A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children with SCID Disorders
Study
phs001392
-
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Study
EGAS00001002684
-
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Study
phs001071
-
Bleomycin Induced Pneumonitis WGS dataset
Dataset
EGAD50000002221
-
Whole transcriptome and 850k methylome profiling of human MBM
Dataset
EGAD00010002281
-
Transcriptomic Analysis of Human Hematopoietic Progenitors from Healthy Donors and Bone Marrow Failure Patients
Study
phs001845
-
Circulating Tumor DNA as a Biomarker in Patients with Stage III and IV Wilms Tumor: Analysis from a Children's Oncology Group Trial, AREN0533
Study
phs002847
-
International Age-Related Macular Degeneration Genomics Consortium - Exome Chip Experiment
Study
phs001039
-
Functional Variant rs9344 at 11q13.3 Regulates CCND1 Expression in Multiple Myeloma with t(11;14)
Study
phs003997
-
Whole exome and Transcriptome sequencing of treatment-naïve esophageal adenocarcinoma biopsies and matched peripheral blood mononuclear cells
Dataset
EGAD00001010876
-
Whole exome DNA sequence profiling of spatial biopsies of high grade serous epithelial ovarian cancer
Study
EGAS00001003048
-
Whole-exome/genome sequencing of childhood acute leukemia in Iraq
Dataset
EGAD00001007873
-
RNA-seq samples
Dataset
EGAD00001008393
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
DNA Methylation Profiles of T2D and Control Subjects from the GCAT Cohort Using EPIC v2
Dataset
EGAD00010002740
-
Smartseq2 data of single immune cells in hepatocellular carcinoma
Dataset
EGAD00001005960
-
VCF file, post sample QC
Dataset
EGAD00001000623
-
Systems biology of Colorectal Cancer
Study
EGAS00001000854
-
STAMPEED: Cardiovascular Health Study (CHS) GWAS to identify genetic variants associated with aging and CVD risk factors and events
Study
phs000226
-
Long-read whole genome sequencing of gastric cancer
Study
EGAS50000001607
-
ESGI_Identification_of_novel_genes_and_mechanisms_leading_to_Primary_Ciliary_Dyskinesia
Study
EGAS00001000523
-
Efficacy of nivolumab in pediatric cancers with high mutation burden and mismatch-repair deficiency
Study
EGAS00001007393
-
Single cell RNAseq FASTQ files of three PDAC organoid lines (P28, P40, P47) using SORT-seq
Dataset
EGAD50000002220
-
Average_5hmC_TF_sites
Dataset
EGAD00010002421
-
WGS of IP-DLBCLs
Dataset
EGAD00001007753
-
Cardiovascular Cell Therapy Research Network (CCTRN): A Phase II, RCT of Mesenchymal Stem Cells & Cardiac Stem Cells in Subjects With Ischemic HF (CONCERT HF-BioLINCC)
Study
phs004055
-
Whole genome sequencing of patients with or at risk for HCC
Study
EGAS00001007249
-
DAC - Department of Periodontology, University of Gothenburg, Sweden
Dac
EGAC50000000241
-
Multi-region WGS of a RET fusion positive cancer
Dataset
EGAD00001006878
-
EGA FUSE Client
Documentation
access/download/visualisation/fuse-client
-
PROstate Cancer Medically Optimized Genome Enhanced ThErapy (PROMOTE) of Castration Resistant Prostate Cancer (CRPC) Patients Treated with Abiraterone Acetate
Study
phs001141
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 17)
Dataset
EGAD50000002409
-
WES of der(1;7)(q10;p10)
Dataset
EGAD50000000986
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetic and Phenotypic Determinants of Blood Pressure and Other Cardiovascular Risk Factors
Study
phs002236
-
Whole-genome variant calling of individuals from the study of allergic diseases in the Canary Islands
Dataset
EGAD50000000429
-
Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors
Study
phs001658
-
Single-cell RNA-seq of human kidney tumors
Dataset
EGAD00001009306
-
Radiation-Related Genomic Profile of Papillary Thyroid Cancer after the Chernobyl Accident
Study
phs001134
-
COVID-19-Induced Immune Alterations in Infants
Study
phs002655
-
Pre-existing immunity drives the response to neoadjuvant chemotherapy in esophageal adenocarcinoma
Study
EGAS00001007245
-
Peripheral blood DNA transcriptomics of ustekinumab treatment response in patients with Crohn's disease
Dataset
EGAD50000000386
-
Peripheral blood DNA transcriptomics of vedolizumab treatment response in patients with Crohn's disease
Dataset
EGAD50000000385
-
10x Genomics raw data of intestinal plasma cells
Dataset
EGAD50000000342
-
Federated discovery and sharing of genomic data using Beacons
Blog
federated-discovery-using-beacons
-
fragmentomic features of individuals with different cfDNA concentrations
Dataset
EGAD50000000970
-
eMERGE: Northwestern (NUgene) WGS
Study
phs001191
-
Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT)
Study
phs001331
-
Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
-
Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain
Study
phs000249
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
Study
phs000421
-
ALLELE Consortium Glioblastoma Project
Study
phs003000
-
Genomic Factors Involved in Chromosome Rearrangements
Study
phs000845
-
CRISPR-Mediated ASD Gene Knockout Reduces Neuronal Activity
Study
phs001816
-
Longitudinal sampling in relapsed and refractory Hodgkin lymphoma
Dataset
EGAD50000000210
-
PIAMA DNA methylation dataset
Dataset
EGAD00010002263
-
PHRT longitudinal ovarian cancer dataset
Dataset
EGAD50000002064
-
Study to investigate the prevalence of leukaemic mutations in whole blood DNA in a cohort of blood donors
Dataset
EGAD00001001319
-
Finnish_population_cohort_genotyping_B
Study
EGAS00001001047
-
NIH Human Microbiome Project - Core Microbiome Sampling Protocol A (HMP-A)
Study
phs000228
-
RNA Splicing Dysregulation in the Pathogenesis of Chronic Lymphocytic Leukemia
Study
phs003191
-
CAGE Profiling of ncRNAs in Hepatocellular Carcinoma Reveals a Strong Activation of Retroviral LTR Promoters in Virus-Induced Tumors
Study
phs000885
-
Identification of Recurrent NAB2-STAT6 Gene Fusions in Solitary Fibrous Tumor by Integrative Sequencing
Study
phs000567
-
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Study
phs000424
-
Platinum Genomes
Study
phs001224
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
Genome Studies in Hereditary Spastic Paraplegia
Study
phs001080
-
Merged VCF file from sporadic Meniere disease cohort
Dataset
EGAD50000001683
-
Merged VCF file from familial Meniere disease cohort
Dataset
EGAD50000001682