-
Genotype data for The admixture histories of Cabo Verde - genotype data
Dataset
EGAD00001008979
-
Genetic background for the major psychiatric disorders in the general Finnish population
Dataset
EGAD00001001250
-
BASIS RNAseq
Dataset
EGAD00001001264
-
Neuroblastoma relapse trio series from the AMC
Dataset
EGAD00001001360
-
Whole genome sequencing in 1038 index cases reveals novel causative genes in pulmonary arterial hypertension
Dataset
EGAD00001003423
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Dataset
EGAD00001005467
-
Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas
Dataset
EGAD00001003315
-
HSP90 inhibitor resistant K562 cells
Dataset
EGAD00001009051
-
DERMATLAS: Hidradenoma papilliferum_WES
Dataset
EGAD00001015481
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
ENU-CCK-81 cetuximab pilot project
Dataset
EGAD00001001947
-
Assessment of genetic and epigenetic variation in human IPS cells-RNA
Dataset
EGAD00001000604
-
Locally advanced rectal cancer samples
Dataset
EGAD00001004378
-
Single-cell omics data for COVID-19 patients
Dataset
EGAD00001009331
-
Chromatin accessibility maps of chronic lymphocytic leukemia identify subtype-specific epigenome signatures and transcription regulatory networks
Dataset
EGAD00001002110
-
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
-
Epigenetic dysregulation in autism spectrum disorder
Dataset
EGAD00001002725
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Dataset
EGAD00001001356
-
Metastatic Breast Cancer Whole Genome
Dataset
EGAD00001000899
-
PacBio Rare Disease Study
Dataset
EGAD00001015611
-
The Natural History of Human Prostate Cancer
Dataset
EGAD00001000689
-
Mapping genetic variants underlying gene regulation in healthy intestinal cell types to identify novel IBD drug targets
Dataset
EGAD00001006331
-
Egypt Genome Project - low coverage whole genome sequencing
Dataset
EGAD00001001372
-
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
-
Cancers of Unknow Primary
Dataset
EGAD00001009426
-
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
-
Assessment of genetic and epigenetic variation in human IPS cells
Dataset
EGAD00001000798
-
TGS - Comprehensive Molecular Characterization of Colorectal Cancer Metastases (2015-07-02)[MOSAIC]
Dataset
EGAD00001001426
-
RNAseq dataset for MALT1 in MCL
Dataset
EGAD00001009771
-
Whole-Genome Sequences from five human populations of Sudan
Dataset
EGAD00001015636
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (RNA-Seq for mature neutrophil, on genome GRCh37)
Dataset
EGAD00001002675
-
Sequencing data for ICGC Oesophageal Adenocarcinoma tissue samples - 129_rnaseq
Dataset
EGAD00001002260
-
Whole genome sequence of third generation family member (SFHS)
Dataset
EGAD00001001454
-
Selection of somatic escape variants in SERPINA1 in liver tissue of patients with alpha-1 anti-trypsin deficiency - WGS
Dataset
EGAD00001015430
-
GILD-ExomeSeq-PTNHL
Dataset
EGAD00001001986
-
Genetic landscape of Extranodal NK/T-cell lymphoma
Dataset
EGAD00001009852
-
ENU-NCI-H508 cetuximab fixed concentration project
Dataset
EGAD00001001948
-
Targeted sequencing of genes recurrently mutated in AML
Dataset
EGAD00001000606
-
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
-
Whole-exome sequencing of 20 samples of actinic keratosis (10s) and cutaneous squamous cell carcinoma (10s)
Dataset
EGAD00001003765
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Dataset
EGAD00001002266
-
Epigenome maps of time-resolved monocyte to macrophage differentiation and innate immune memory
Dataset
EGAD00001002693
-
BASIS BC WGS Dataset
Dataset
EGAD00001001337
-
HELIUS cohort gut microbiome
Dataset
EGAD00001004106
-
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
-
FinHer Breast Cancer Study
Dataset
EGAD00001000871
-
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
-
Ancestry and somatic profile predict acral melanoma origin and prognosis – WXS
Dataset
EGAD00001015755
-
A next-generation dual guide CRISPR system for genetic interaction library screening
Dataset
EGAD00001015754
-
Ovarian Cancer Organoid Biobank
Dataset
EGAD00001004387
-
Chromosome Segregation Errors Promote a Diverse Spectrum of Simple and Complex Genomic Rearrangements
Dataset
EGAD00001004163
-
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
-
Paroxysmal Neurological Disorders 2
Dataset
EGAD00001000407
-
Congenital anosmia 1
Dataset
EGAD00001002210
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Dataset
EGAD00001015343
-
WGoxBS and SureSelect data of the POPS placenta samples
Dataset
EGAD00001003136
-
Genetics of gene expression in human macrophage response to Salmonella
Dataset
EGAD00001003204
-
Genetic architecture of male infertility in India
Dataset
EGAD00001015606
-
BLUEPRINT EpiVar ChIP-seq in lineage specifying transcription factors
Dataset
EGAD00001004571
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers: multi-timepoint exome sequencing of a single patient's disease
Dataset
EGAD00001003769
-
The British Autozygosity Populations BioResource
Dataset
EGAD00001003215
-
The molecular landscape of colorectal cancer reveals genetic mutations(5 cases)
Dataset
EGAD00001003223
-
Genetic profiling of mucosal melanoma
Dataset
EGAD00001003237
-
The molecular landscape of colorectal cancer reveals genetic mutations - COCA-CN
Dataset
EGAD00001003304
-
March 2017 data update (bam/fastq) (containing H3K27ac for CEMT_87, RNA-Seq for CEMT_141, CEMT_142, CEMT_145, CEMT_146, H3K27me3, H3K9me3, H3K4me3, H3K4me1, ChIP-Seq Input for CEMT_88, CEMT_90 and CEMT_91) 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
EGAD00001003272
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Dataset
EGAD00001003409
-
TRACERx100 metastatic samples
Dataset
EGAD00001003301
-
Autozygosity pilot - Born in Bradford (2017-05-11)
Dataset
EGAD00001003329
-
Molecular diagnosis of albinism (2018-03-14)
Dataset
EGAD00001004039
-
Congenital mesoblastic nephroma and infantile fibrosarcoma
Dataset
EGAD00001003884
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Dataset
EGAD00001004157
-
The landscape of somatic mutation in normal colorectal epithelial cells
Dataset
EGAD00001004193
-
Genetic Heterogeneity of the familial gastric neuroendocrine tumors (2018-06-06)
Dataset
EGAD00001004153
-
IBD Whole Genome Sequencing Phase 1 (2018-08-03)
Dataset
EGAD00001004272
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015477
-
DERMATLAS: Hidradenoma papilliferum_RNAseq
Dataset
EGAD00001015480
-
Congenital Heart Disease in UK Families
Dataset
EGAD00001000343
-
Exome sequencing of patients with rare neurological disorders
Dataset
EGAD00001000346
-
Whole-exome sequencing of rare autoimmune-related phenotypes
Dataset
EGAD00001000408
-
Genetics of Microcephalic Osteodysplatics Primordial Dwarfism
Dataset
EGAD00001000342
-
A study of the molecular pathogenesis of Splenic Marginal Zone and Diffuse Large B-Cell Lymphoma
Dataset
EGAD00001000410
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004413
-
Osteosarcoma RNAseq
Dataset
EGAD00001000826
-
Mapping Cells and Interactions in the Thymus Across Development and Aging (2025-07-28)
Dataset
EGAD00001015660
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004416
-
Whole Genome sequencing of individuals from Val Borbera, Italy
Dataset
EGAD00001000731
-
Characterization of genomic landscape of Peripheral T-cell Lymphomas, not otherwise specified (PTCL-NOS) (2018-10-30)
Dataset
EGAD00001004428
-
Ovarian Cancer Organoid Biobank - RNASeq data
Dataset
EGAD00001004509
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Dataset
EGAD00001004554
-
PKD1 capture-by-hybridization resequencing for genetic diagnostics of polycystic kidney disease
Dataset
EGAD00001001091
-
BLUEPRINT: Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Dataset
EGAD00001001011
-
Genetic background for cardio vascular disorders in the general Finnish population
Dataset
EGAD00001001251
-
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Dataset
EGAD00001001441
-
Constitutional and somatic genomic rearrangements coherently restructure chromosome 21 in acute lymphoblastic leukaemia
Dataset
EGAD00001000658
-
Integrated genomic characterization of adrenocortical carcinoma
Dataset
EGAD00001000764
-
Assessment of epigenetic variation in human iPS cells-Medip
Dataset
EGAD00001000827
-
Autozygosity pilot - British-Pakistani from Birmingham
Dataset
EGAD00001001025