-
hereditary BrEAst Case CONtrol study
Study
EGAS00001005043
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
Origins and timing of emerging lesions in advanced renal cell carcinoma
Study
EGAS00001005897
-
Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001002598
-
The European Bank for Induced Pluripotent stem cells (EBiSC) is designed to address the increasing demand by iPSC researchers for quality-controlled, disease-relevant research grade iPSC lines, data and cell services.In this study Whole Genome Sequencing was performed on a selection of lines from the project.
Study
EGAS00001002755
-
Gastric_Mutational_Signatures__GMS_
Study
EGAS00001002939
-
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
Alveolar Rhabdomyosarcoma case report
Study
EGAS00001004828
-
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
EPIC arrays data for chemotherapy response project
Study
EGAS00001004515
-
Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes
Study
EGAS00001005541
-
RNA sequencing of undifferentiated sarcomas
Study
EGAS00001003291
-
Mutational landscape of eccrine porocarcinoma (sweat gland tumour)
Study
EGAS00001004632
-
Using human induced pluripotent stem cell-derived oligodendrocytes to explore cellular phenotypes associated with t(1;11) translocation.
Study
EGAS00001004595
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis
Study
EGAS00001006187
-
Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data
Study
EGAS00001003504
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data
Study
EGAS00001006388
-
Time-dependent characterization of CNS response in COVID-19
Study
EGAS00001006442
-
T cell reactivity of MHC epitopes
Study
EGAS00001006445
-
Multiple Sclerosis risk variants regulate gene expression in innate and adaptive immune cells
Study
EGAS00001004087
-
Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
Study
EGAS00001005071
-
Identification and functional characterisation of a rare MTTP variant underlying familial non-alcoholic fatty liver disease
Study
EGAS00001005254
-
Transcriptomic analysis of cell-of-origin CNS neuroblastoma, FOXR2 activated
Study
EGAS00001007247
-
Human data for chromatin accessibility (ATAC-Seq and scATAC-Seq) and transcriptome (RNA-Seq and scRNA-Seq) in eight B-cell precursors, from HSC to Naive B cells
Study
EGAS00001007296
-
Genomic profiling of IBC
Study
EGAS00001007520
-
Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Study
EGAS00001007569
-
MethylScan data of plasma samples
Dataset
EGAD00001015815
-
Whole exome sequencing of a representative cohort of AML
Dataset
EGAD00001007580
-
Somatic mutation rates scale with lifespan across mammals
Dataset
EGAD00001008032
-
Targeted de novo phasing and long-range assembly by template mutagenesis
Dataset
EGAD00001008444
-
Targeted Myeloid DNA-Panelsequencing, MLL
Dataset
EGAD00001008485
-
Sperm sequencing reveals extensive positive selection in the human germline -NanoSeq
Dataset
EGAD00001015590
-
TB-DAR Whole Genome Sequencing Study
Dataset
EGAD00001008400
-
Sperm sequencing reveals extensive positive selection in the human germline -TargetedNanoSeq
Dataset
EGAD00001015591
-
59 CLPD-NK cases WGS & WTS data
Dataset
EGAD00001008558
-
The 5-hydroxymethylcytosine Landscape of Prostate Cancer
Dataset
EGAD00001008462
-
Dataset for colorectal_cancer-RNA
Dataset
EGAD00001008855
-
Sperm sequencing reveals extensive positive selection in the human germline -WGS
Dataset
EGAD00001015592
-
Single-cell RNA-sequencing of CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) from a Phase I clinical study in paediatric ALL: CARPALL
Dataset
EGAD00001010018
-
Whole-exome sequencing of hepatocellular carcinoma biopsies
Dataset
EGAD00001008182
-
BARIA 100 transcriptomics
Dataset
EGAD00001009092
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
-
Whole exome sequencing of tumors from the Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Dataset
EGAD00001010928
-
Clonal haematopoiesis in patients with AAA (2019-04-03)
Dataset
EGAD00001004895
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-009
Dataset
EGAD00001006027
-
CINECA synthetic data.Please note: This study contains synthetic data (with cohort “participants” / ”subjects” marked with FAKE) has no identifiable data and cannot be used to make any inference about cohort data or results.
Study
EGAS00001002472
-
Dual spatially resolved transcriptomics for human host-pathogen colocalization studies in FFPE tissue sections
Study
EGAS00001006186
-
DAC Portal documentation
Documentation
access/data-access-committee/dac-portal
-
ICGC Data Access Compliance Office
Dac
EGAC00001000010
-
DAC for Central African ancient demography processes NGS dataset
Dac
EGAC50000000447
-
Projects
Documentation
about/projects-and-funders/projects
-
Spatial transcriptomic data of breast cancer
Dataset
EGAD50000000322
-
Tracing tumor evolution and heterogeneity of pleomorphic carcinoma of the lung
Study
EGAS50000000314
-
Capmatinib shows superior efficacy for MET-fusion driven pediatric high-grade glioma and synergizes with radiotherapy
Study
EGAS50000000137
-
Cergentis FFPE-TLC
Study
EGAS50000000427
-
NGS-based monitoring of the T cell receptor repertoire in living donor kidney transplant patients undergoing combination cell therapy
Study
EGAS50000000210
-
Combined single-cell transcriptomics and T-cell receptor sequencing reveal heterogeneity of mycosis fungoides between and within patients and identify a CD4+ cytotoxic subtype
Study
EGAS50000000226
-
DAC for Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Dac
EGAC50000000332
-
Transcriptome analysis of human longitudinal whole blood samples from PCR-positive and PCR-negative adults following controlled inoculation with Influenza A (H3N2) virus.
Study
EGAS50000000679
-
AYA glioma NGS
Study
EGAS50000000383
-
Mapping Genotypes to Chromatin Accessibility Profiles in Single Cells
Study
EGAS50000000164
-
Fragmentomic features of individuals with different cfDNA concentrations
Study
EGAS50000000692
-
RNAseq samples of patients with anti-PD-1 resistant HNSCC from a non-randomized, open-label phase 1b clinical trial
Study
EGAS50000000728
-
WES samples of patients with anti-PD-1 resistant HNSCC from a non-randomized, open-label phase 1b clinical trial
Study
EGAS50000000729
-
Synchronous patterning of hiPSC-derived CNS progenitors generates comprehensive axial spinal cord organoids (CASCOs) containing diverse motor neuron population
Study
EGAS50000000891
-
Gliomas, glioneuronal and neuronal tumors
Dataset
EGAD50000000300
-
Ultrasensitive Detection and Monitoring of Circulating Tumor DNA using Structural Variants in Early-Stage Breast Cancer
Study
EGAS50000000799
-
Genome-wide NanoRCS sequencing of cfDNA and ctDNA from liquid biopsies of healthy individuals and cancer patients
Study
EGAS50000000154
-
Multi-omics profiling identifies two epithelioid sarcoma molecular subtypes with distinct signaling and immune characteristics
Dac
EGAC50000000552
-
Clinical Outcomes of 344 Diffuse Large B-Cell Lymphoma patients
Study
EGAS50000001054
-
DAC for Genomic landscapes of endometrioid and mucinous ovarian cancers and morphologically similar tumor types
Dac
EGAC50000000341
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
The acute effects of morning bright light on the human white adipose tissue transcriptome: exploratory post hoc analysis
Study
EGAS50000001206
-
Longitudinal analysis of bone marrow heterogeneity reveals the co-evolution of malignant B cells and their T-cell niche supporting follicular lymphoma persistence
Study
EGAS50000001295
-
RNA sequencing data from patient derived colorectal cancer organoids
Study
EGAS50000000685
-
DCIS Whole Exome & Whole Genome Sequencing Data
Dataset
EGAD50000001846
-
Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Study
EGAS00000000115
-
Single cell RNAseq data of human neurons, Bouwen et al Nat Comm 2025
Study
EGAS50000001369
-
Profiling the genomic landscape and evolutionary history of polyploid giant cancer cells in undifferentiated pleomorphic sarcomas
Study
EGAS50000001445
-
Investigating the differences in iPSC-derived intestinal epithelial cell behaviour and composition grown as organoid, in Transwell or Intestine-Chip.
Study
EGAS50000001339
-
A human induced pluripotent stem cell toolbox for studying sex chromosome effects-Whole exome seq
Study
EGAS50000000930
-
Single cell transcriptome and TCR sequencing of EBNA1, ANO2 and CRYAB-reactive T cells in multiple sclerosis.
Study
EGAS50000001531
-
Single cell transcriptomics to characterize the tumor microenvironment of prostate cancer fusion biopsies
Study
EGAS50000000888
-
Characterization of the cellular microenvironment in fibrostenotic Crohn’s disease
Study
EGAS50000000382
-
Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
-
Spatial map of microglia states across CNS diseases
Study
EGAS50000001289
-
Multiplexed biomarkers dynamically detect heterogeneous residual neuroblastoma cell clone activity in the bone marrow niche
Study
EGAS50000001581
-
DPY30_ChIP_seq
Study
EGAS00001001132
-
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Study
EGAS00001000599
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
-
Targeting PTPRK-RSPO3 colon tumours promotesdifferentiation and loss of stem-cell function
Study
EGAS00001001462
-
RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the SardiNIA cohort.
Study
EGAS00001002105
-
Assessment of de novo copy number variations in Italian patients with schizophrenia.
Study
EGAS00001002159
-
Genomic landscape of Ewing sarcoma (ICGC project)
Study
EGAS00001000855
-
Genome-wide mutation analysis of germinal-center B-cell derived lymphomas within the ICGC MMML-Seq Consortium
Study
EGAS00001000394
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
-
Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected
Study
EGAS00001000769
-
Integrative_Oncogenomics_of_multiple_myeloma
Study
EGAS00001000244
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Study
EGAS00001000958
-
Exome sequencing of 1000 population control samples from the UK 1958 birth cohort
Study
EGAS00001000971
-
Pilot_experiment_on_functional_genomics_in_osteoarthritis_RNA
Study
EGAS00001001203
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
-
Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium
Dataset
EGAD00001002738
-
WGS and WTS data of patient diagnosed with HSTCL
Dataset
EGAD00001005229
-
RNA sequencing of periprostatic fat after a 6 month deep androgen deprivation therapy
Dataset
EGAD00001004971
-
Molecular profiling of tissue autopsies and ctDNA
Dataset
EGAD00001007040
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Dataset
EGAD00001007872
-
GCT WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003267
-
Spatial heterogeneity of follicular lymphoma
Dataset
EGAD00001003553
-
CCOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003265
-
Whole transcriptome RNA sequencing on bone marrow and peripheral blood samples from patients with acute myeloid leukemia at diagnosis or relapse.
Dataset
EGAD00001004187
-
GoNL aligned sequence data in BAM format.
Dataset
EGAD00001001038