-
ITER-FIISC Data Access Committee (FPF)
Dac
EGAC50000000473
-
LOPEZ_2019.vcf.gz
Dataset
EGAD00010002100
-
Purple copy number segments for EGAS00001004572
Dataset
EGAD00001006908
-
INdiana GENomics: Implementing an Opportunity for the Under Served (INGENIOUS)
Study
phs001701
-
Precision Medicine for ABCA4 Disease: Modifier Alleles
Study
phs002393
-
Coronary Artery Risk Development in Young Adults (CARDIA) Study - Gene Environment Association Studies Initiative (GENEVA)
Study
phs000309
-
Hofer et al., A specific subpopulation of cancer-associated fibroblasts promotes resistance to chemotherapy in triple-negative breast cancer by upregulating G0S2 protein
Study
EGAS50000000886
-
Studies of Left Ventricular Dysfunction (SOLVD-BioLINCC)
Study
phs003668
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD-BioLINCC)
Study
phs003551
-
Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families
Study
phs001675
-
scRNAseq for patients with immunodeficiency and HCs
Study
EGAS00001007271
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs001088
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
Genomic Basis of Phenotypic Variability of Complex Disorders
Study
phs002450
-
Targeting FGFR1 for treatment of soft-tissue sarcoma (H021)
Study
EGAS00001001844
-
All you need to know about the new Submitter Portal
Blog
new-submitter-portal
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Genomic Sequencing of Lung Adenocarcinoma
Study
phs000488
-
NHLBI TOPMed: Women's Health Initiative (WHI)
Study
phs001237
-
A Comprehensive Genomic Study of Pediatric Malignancy
Study
phs001928
-
Single-nucleus chromatin accessibility profiling of human fetal liver hematopoiesis (10x Multiome)
Study
EGAS50000001632
-
Single-nucleus gene expression profiling of human fetal liver hematopoiesis (10x Multiome)
Study
EGAS50000001631
-
Papua New Guinean Lowlanders Dataset
Study
EGAS50000000033
-
Single-cell targeted DNA-sequencing and protein sequencing
Study
EGAS50000000580
-
Analysis of copy number variation landscape of glioma by shallow coverage whole genome sequencing
Study
EGAS00001003690
-
Identification of fusion transcripts by RNA-sequencing and Whole genome sequencing of a METABRIC patient sample
Study
EGAS00001002475
-
Myelodysplastic_syndrome_whole_genomes
Study
EGAS00001000291
-
Integrative_Oncogenomics_of_multiple_myeloma
Study
EGAS00001000243
-
Myeloproliferative_Disease_Whole_Genomes
Study
EGAS00001000290
-
Biological insights from the whole genome sequences of human embryonic stem cell lines
Study
EGAS00001002400
-
Gene_regulation_of_human_CD4__Treg_cells_
Study
EGAS00001003516
-
Stratton__WGS___Identification_of_Early_Life_Exposures_in_Paediatric_Colonic_Crypts_of_Healthy_Individuals
Study
EGAS00001007921
-
Whole Genome Sequences of 18th century African descended individuals from Charleston, South Carolina.
Study
EGAS00001006693
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
Dataset for "HPV integration induces gene fusions" (Illumina)
Dataset
EGAD50000001305
-
RNA-seq data for genomic determinants of response and resistance to inotuzumab in B-ALL
Dataset
EGAD50000000095
-
WGS data for genomic determinants of response and resistance to inotuzumab in B-ALL
Dataset
EGAD50000000096
-
GenomeDenmark Phase 2 - variants called on chrY for 62 males.
Dataset
EGAD00001003186
-
single cell RNASEQ files for Mullighan BiTE RNASEQ3
Dataset
EGAD00001005733
-
H3Africa ReMAC Shotgun Metagenomic Phenotype
Dataset
EGAD00001006244
-
Genome-wide data for 11 Roma individuals
Dataset
EGAD00001007773
-
A Single-cell Atlas of Progressive TKI Resistance in Chronic Myeloid Leukemia
Dataset
EGAD00001007946
-
WGS of NPC268_Tumor and NPC268_Cell_line
Dataset
EGAD00001010292
-
Oncoprint GSCCs
Dataset
EGAD00001011276
-
NHLBI TOPMed: Lung Tissue Research Consortium (LTRC)
Study
phs001662
-
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Study
EGAS00001006059
-
Accurate Genome-Wide Germline DNA Profiling from Decade-Old Archival Tissue Specimens
Study
phs002865
-
Breakpoint detection using long insert whole genome sequencing
Study
phs000646
-
Genetics of Antinuclear Antibodies
Study
phs003189
-
Integrated multi-omics analysis of pediatric hepatoblastoma
Study
JGAS000188
-
PROMETEO
Study
EGAS50000001499
-
Cancer and germline exomes, and cancer RNA-seq consisiting of FASTQ paired-end reads from melanoma, lung and colon cancer samples
Study
EGAS00001005513
-
Lenalidomide Resistance in del(5q) Myelodysplastic Syndrome Follows Loss of RUNX1/TP53-mediated Megakaryocytic Differentiation
Dataset
EGAD00001005769
-
RNA-sequencing of ex vivo exhausted human antigen-specific T cells
Dataset
EGAD00001009754
-
Understanding the development of resident memory T cells (Trm) in the human small intestine using integrative multiomic approaches: Adult RNA (2025-10-14)
Dataset
EGAD00001015739
-
McQuillin_Global_London_SCZ_Bipolar_WES
Dac
EGAC50000000311
-
ASPSCR1-TFE3 gene fusion panel deep amplicon sequencing data
Dataset
EGAD50000002438
-
Evolution of neoantigen landscape during immune checkpoint blockade in non-small cell lung cancer
Dataset
EGAD00001004336
-
Exome sequencing in bipolar disorder families
Dataset
EGAD00001004276
-
Transcriptome profiling for Korean Early Onset Gastric Cancer
Dataset
EGAD00001002187
-
FACS-based purification and paired-end RNA sequencing
Dataset
EGAD00001007687
-
Detection of Cancer Mutations by Urine Liquid Biopsy in 12 Bladder Cancer Patients
Dataset
EGAD00001008429
-
Whole Genome Bisulfite sequencing data for Oncogenic 3D genome conformations identify novel therapeutic targets in ependymoma
Dataset
EGAD00001008805
-
RNA-Sequencing of B-Lymphoblastic Leukemia with Glucocorticoids and PI3K Delta Inhibition
Study
phs003085
-
Enhanced Adjuvanticity of a Personal Neoantigen Vaccine Generates Potent Neoantigen-Specific Immunity
Study
phs003919
-
ITER-FIISC Data Access Committee (Sepsis)
Dac
EGAC50000000641
-
LOGGIC Core BioClinical Data Bank: Added clinical value of RNA-Seq in an international molecular diagnostic registry for pediatric low-grade glioma patients
Study
EGAS00001007072
-
Single cell sequencing in D425
Dataset
EGAD50000002304
-
Batch1-2_Genotypes_PostQC
Dataset
EGAD00010002127
-
GWAS results from Danjou et al, Nature Genetics 2015
Dataset
EGAD00010001722
-
Germline snv g.vcf for EGAS00001004572
Dataset
EGAD00001006910
-
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): a Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study - for Samples Collected at Johns Hopkins
Study
phs003094
-
BPH Tissues for Cell Culture and Analysis - A Patient-Derived Xenograft Model Using Benign Prostatic Tissues
Study
phs003692
-
DNA Repair Capacity for Lung Disease Risk Assessment
Study
phs004063
-
DNA methylation (RRBS) data for the validation the glioblastoma progression study (GBMatch).
Dataset
EGAD00001004074
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
Long-read-transcriptome-sequencing of CLL and MDS patients uncovers common molecular effects of SF3B1 mutations
Study
EGAS50000000053
-
Endocrine therapy reprogramming of breast cancer facilitates metastatic escape via upregulation of P-Rex1/Rac1 signalling
Study
EGAS00001008353
-
Immune Profiles Study
Study
phs002998
-
Genetics of Lymphatic Anomalies from Center of Applied Genomics (CAG) at CHOP
Study
phs001802
-
The Diabetes Heart Study (DHS)
Study
phs001012
-
A new beta-globin mutation responsible of a beta-thalassemia (HbVar database ID 2928) was observed in 8 unrelated French families. The mutation carriers originated from Nord-Pas-de-Calais, a Northern French region where the chief town is Lille.5 unrelated mutation carriers were genotyped for a set of 12 microsatellites from chromosome 11, around the beta-globin gene. Among the 5 mutation carriers, 4 were genotyped for 97 European Ancestry Informative SNPs (EAIMs). 32 controls from Nord-Pas-de-Calais were genotyped for the microsatellites and SNPs.
Dac
EGAC00001000245
-
Ankara Bilkent City Hospital Clinical Research Ethics Committee
Dac
EGAC50000000940
-
Processed miRNA Counts for the miRNA Profiling from Indian HFrEF Cohort Dataset
Dataset
EGAD50000001195
-
Processed Total RNA Counts for the RNA Profiling from Indian HFrEF Cohort Dataset
Dataset
EGAD50000001193
-
DNA methylation (RRBS) data for the glioblastoma progression study (GBMatch).
Dataset
EGAD00001003427
-
Isotype-resolved sequencing of B-cell receptor in sorted memory populations (2017-09-13)
Dataset
EGAD00001003747
-
Shedding light over COVID-19 susceptibility and severity
Blog
covid-19-susceptibility-and-severity
-
Raw human sequencing data for “Characterization of intestinal immune responses in generalized human and murine lipodystrophy”
Study
EGAS50000001517
-
NHLBI TOPMed: The Genetics and Epidemiology of Asthma in Barbados
Study
phs001143
-
Genomic Regions Associated with Susceptibility to Barrett's Esophagus and Esophageal Adenocarcinoma in African Americans: The Cross BETRNet Admixture Study
Study
phs001454
-
Identification of Recurrent NAB2-STAT6 Gene Fusions in Solitary Fibrous Tumor by Integrative Sequencing
Study
phs000567
-
Resistance to Latent Mycobacterium tuberculosis Infection in South Africa: Immunologic Profiling
Study
phs002746
-
Gabriella Miller Kids First Pediatric Research Program in Whole Genome Sequencing of African and Asian Orofacial Clefts Case-Parent Triads
Study
phs001997
-
Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability
Study
EGAS00001003572
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Study
EGAS00001004064
-
Multi-Omic Microbiome Study-Pregnancy Initiative (MOMS-PI)
Study
phs001523
-
PD-1 antibody-bound progenitor-exhausted CD8+ T cells in lymph nodes boost PD-1-blockade anti-tumor immunity in gastrointestinal cancer
Study
JGAS000720