-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
Lund HPI data access committee for Inspire
Dataset
EGAD00001005523
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
-
Cellular and Molecular Characterization of Renal Cell Carcinoma
Study
phs002252
-
Lund RNAseq data
Dataset
EGAD00001005512
-
Initial cohort of 500 solid tumors screened for Basket of Baskets
Study
EGAS00001005893
-
NIDDK IBD Genetics Consortium Crohn's Disease Genome-Wide Association Study
Study
phs000130
-
Genetic Epidemiology of Lung Cancer Consortium GWAS of Familial Lung Cancer
Study
phs000629
-
Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II)
Study
phs000948
-
National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma
Study
phs000144
-
Pancreatic Cancer Case Control Association Study
Study
phs000648
-
Autism Sequencing Consortium (ASC)
Study
phs000298
-
ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)
Study
phs000631
-
Aggregated panel-seq VCF for initial cohort screened for BoB
Dataset
EGAD00001008437
-
COVID_19_UK_CIC_Spatial
Study
EGAS00001005817
-
McGill Epigenomics Mapping Centre
Study
EGAS00001000995
-
DNA Methylation in Prostate Tumor and Paired Benign Tissue for African and European Ancestry Men
Study
phs003516
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Center Common Disease Genomics [CCDG] - CVD - TAICHI
Study
phs001487
-
African American Multiple Myeloma GWAS
Study
phs001632
-
Whole Genome Association Study of Systemic Lupus Erythematosus
Study
phs000122
-
Genome wide association study for early onset coronary disease and related phenotypes (ADVANCE)
Study
phs000423
-
Multi-Omic Microbiome Study-Pregnancy Initiative (MOMS-PI)
Study
phs001523
-
Proteogenomic Characterization Unveils Biomarkers Associated With Chemoresistance in Muscle Invasive Bladder Cancer
Study
phs004049
-
Myocardial Infarction Genetics Exome Sequencing Consortium: University of Lubeck
Study
phs000990
-
eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics
Study
phs001165
-
Sporadic ALS Australia Systems Genomics Consortium (SALSA-SGC)
Study
phs002068
-
Sequencing data for the manuscript "Resolving spatial subclonal genomic heterogeneity of loss of heterozygosity and extrachromosomal DNA in gliomas"
Dataset
EGAD50000001394
-
DAC Wachten Laboratory and Toma Laboratory, University of Bonn/University Hospital Bonn
Dac
EGAC50000000916
-
International Consortium for Blood Pressure (ICBP)
Study
phs000585
-
Development and Validation of a Disability Severity Index for Charcot-Marie-Tooth Disease (CMT)
Study
phs001295
-
NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG)
Study
phs001608
-
GEnetics of Nephropathy - an International Effort (GENIE) GWAS of Diabetic Nephropathy in the UK GoKinD and All-Ireland Cohorts
Study
phs000389
-
International Consortium on the Genetics of Systemic Lupus Erythematosus (SLEGEN)
Study
phs000216
-
The Genetics of Type 2 Diabetes Consortium (GoT2D): Low-Pass Sequencing and High-Density SNP Genotyping for Type 2 Diabetes
Study
phs000840
-
HPV-associated Cancer Consortium Data Access Committee
Dac
EGAC50000000088
-
Glioma International Case Control Study (GICC)
Study
phs001319
-
Breast Cancer Association Consortium Data Access Coordinating Committee
Dac
EGAC50000000824
-
Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol
Study
phs000575
-
International Consortium to Identify Genes and Interactions Controlling Oral Clefts
Study
phs000094
-
Genome-wide Association Study of Myasthenia Gravis
Study
phs000726
-
Common Variant GWAS, Genetics & Epidemiology of Colorectal Cancer Consortium (GECCO)
Study
phs001078
-
University of Helsinki Systems Biology and Turku University Hospital Data Access Committee
Dac
EGAC00001001937
-
Cellular Origins and Genetic Landscape of Cutaneous GD T Cell Lymphoma
Study
phs001969
-
University of Helsinki Systems Biology and Turku University Hospital Data Access Committee
Dac
EGAC00001001978
-
Department of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
Dac
EGAC00001003284
-
Yale Center for Mendelian Genomics (YCMG)
Study
phs000744
-
T2D-GENES: Exome sequencing
Study
EGAS00001001460
-
Research Data Office, Lund University
Dac
EGAC50000000619
-
MOSAIC - Multi-Omics Spatial Atlas In Cancer
Study
EGAS50000000689
-
Washington University Coronary Artery Disease Study
Study
phs001227
-
NeuroCHARGE Consortium GWAS of White Matter Hyperintensities on MRI
Study
phs002227
-
DAC Department of Neurology, TUM University Hospital, Technical University of Munich, School of Medicine and Health
Dac
EGAC00001003508
-
Uppsala University Data Access Committee
Dac
EGAC50000000433
-
NABEC: North American Brain Expression Consortium
Study
phs001300
-
Exome sequencing of United Kingdom Brain Expression Consortium samples
Study
EGAS00001002113
-
February 2021 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001007919
-
June 2018 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001004300
-
Drug development for pediatric cancers: the importance of patient' s genomic data re-use
Blog
drug-development-for-pediatric-cancers
-
AfricanNeo_B dataset
Dataset
EGAD50000000006
-
AfricanNeo_C dataset
Dataset
EGAD50000000009
-
AfricanNeo_D dataset
Dataset
EGAD50000000010
-
Multiple Sclerosis Replication Chip data (MS Chip)
Study
EGAS00001003216
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Multi-Ethnic Study of Atherosclerosis (MESA)
Study
phs003017
-
DAC for Greenland Studies of University of Copenhagen and University of Southern Denmark.
Dac
EGAC00001000736
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
HCEMM - Semmelweis University Molecular Oncohematology Research Group DAC
Dac
EGAC50000000091
-
Okayama University Hospital, CGM center, DAC
Dac
EGAC50000000250
-
EGAD00010000807
Dataset
EGAD00010000807
-
AfricanNeo_A dataset
Dataset
EGAD50000000008
-
AfricanNeo_E dataset
Dataset
EGAD50000000011
-
Pancreatic Cancer Sequencing Initiative
Study
EGAS00001000343
-
University of Helsinki and Turku University Hospital Data Access Committee
Dac
EGAC00001001760
-
May 2019 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001005060
-
August 2020 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001006383
-
August 2019 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001005335
-
Udated data for October 2017 data release for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003906
-
January 2018 data update (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003962
-
June 2017 data update (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003414
-
September 2016 data update (bam/fastq/vcf) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001002724
-
March 2016 update of Whole genome bisulfite sequencing assay data (bams) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001987
-
Population Architecture using Genomics and Epidemiology (PAGE)
Study
phs000356
-
GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Study
EGAS00001001459
-
dbGaP Collection: Psychiatric Genomics Consortium (PGC) dbGaP Datasets
Study
phs001254
-
DAC Johns Hopkins University - AML scRNAseq study
Dac
EGAC50000000242
-
WTCCC3_Anorexia_Nervosa
Study
EGAS00001000913
-
eMERGE: Northwestern (NUgene) WGS
Study
phs001191
-
Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC)
Study
phs001222
-
Charles University - Hemminki Lab DAC
Dac
EGAC50000000393
-
DAC of "Gene expression adaptation of metastases to their host tissue"
Dac
EGAC50000000514
-
Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (RNA-Seq)
Study
JGAS000028
-
Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (WGBS)
Study
JGAS000026
-
Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (ChIP-seq)
Study
JGAS000027
-
February 2020 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001006220
-
December 2016 data update (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003122
-
June 2016 data update for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001002239
-
March 2016 update of Whole genome bisulfite sequencing assay data (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001957
-
March 2016 update of whole genome shotgun sequencing data (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001958
-
March 2016 update of smRNA-Seq assays data (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001959
-
DAC for DRS peripheral blood, University Medical Center Johannes Gutenberg University Mainz
Dac
EGAC50000000667