-
Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Dataset
EGAD00001010176
-
Clonal origin of lineage switch leukemia following CAR-T cell and blinatumomab therapy
Dataset
EGAD00001009161
-
DERMATLAS: Hidradenoma papilliferum_RNAseq
Dataset
EGAD00001015480
-
Epigentic sequence data of monocytes and macrophages
Dataset
EGAD00001002201
-
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Dataset
EGAD00001009647
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments. (2019-06-10)
Dataset
EGAD00001005082
-
PacBio Rare Disease Study
Dataset
EGAD00001015611
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Dataset
EGAD00001009668
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
ESGI-Exome sequencing in Circulating Tumor Cells to determine therapy related markers
Dataset
EGAD00001001425
-
RNAseq Atlas in HCC tumors
Dataset
EGAD00001015341
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - WGS
Dataset
EGAD00001009793
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - RNA-Seq
Dataset
EGAD00001009794
-
Triple Negative Breast Cancer RNA Sequencing
Dataset
EGAD00001000390
-
Chromatin 3D interactions mediate genetic effects on gene expression (ChIP-seq)
Dataset
EGAD00001004871
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Dataset
EGAD00001009847
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
FinHer Breast Cancer Study
Dataset
EGAD00001000871
-
Genomic Advances in Sepsis (GAinS) genotyping
Dataset
EGAD00001015369
-
Human Origins array data for 1510 individuals
Dataset
EGAD00001010015
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS)
Dataset
EGAD00001003130
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Dataset
EGAD00001003246
-
The molecular landscape of colorectal cancer reveals genetic mutations(17 cases)
Dataset
EGAD00001003224
-
Evolutionary Genome Analysis of Transformation into Small Cell Carcinomas from Lung Adenocarcinomas
Dataset
EGAD00001003315
-
Dataset of whole genome bisulfite data of 4 different monocyte samples
Dataset
EGAD00001003259
-
Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
-
Genetic factors underlying premature MI in Greek families without vessel disease
Dataset
EGAD00001002178
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Dataset
EGAD00001011067
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (RNA-Seq for CD4-positive, alpha-beta T cell, on genome GRCh37)
Dataset
EGAD00001002671
-
Genetic profiling of mucosal melanoma
Dataset
EGAD00001003237
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGS)
Dataset
EGAD00001005017
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183
-
GNAI1 CGH Array
Dataset
EGAD00001007742
-
Xenograft BC WGS Dataset
Dataset
EGAD00001001336
-
Exome sequencing of UK Birth Cohorts - Born in Bradford
Dataset
EGAD00001015370
-
Next gen seq of eye cancers (2019-08-14)
Dataset
EGAD00001005251
-
Congenital mesoblastic nephroma and infantile fibrosarcoma
Dataset
EGAD00001003885
-
Exome sequencing of serially transplanted genetically marked IC-enriched primary PDAC cultures.
Dataset
EGAD00001000884
-
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
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cells, (ChIP-Seq_H3K4me3 for mature neutrophil, on genome GRCh37)
Dataset
EGAD00001002711
-
Somatic mutations of 256 whole-genome sequenced colorectal cancer tumors.
Dataset
EGAD00001004329
-
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
-
BASIS RNAseq
Dataset
EGAD00001001264
-
Low coverage whole-genome sequencing of samples from the Cretan Greek isolate collection HELIC-MANOLIS
Dataset
EGAD00001001637
-
DNMT3A-R882 mutations intrinsically drive dysfunctional neutropoiesis from human haematopoietic stem cells
Dataset
EGAD00001015750
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
HSP90 inhibitor resistant K562 cells
Dataset
EGAD00001009051
-
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
-
Balanced Ependymoma
Dataset
EGAD00001000350
-
Paroxysmal neurological Disorders
Dataset
EGAD00001000412
-
Assessment of genetic and epigenetic variation in human IPS cells-RNA
Dataset
EGAD00001000604
-
Locally advanced rectal cancer samples
Dataset
EGAD00001004378
-
Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Dataset
EGAD00001008317
-
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
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Dataset
EGAD00001001356
-
Mapping genetic variants underlying gene regulation in healthy intestinal cell types to identify novel IBD drug targets
Dataset
EGAD00001006331
-
The Natural History of Human Prostate Cancer
Dataset
EGAD00001000689
-
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
-
Egypt Genome Project - low coverage whole genome sequencing
Dataset
EGAD00001001372
-
Characterization of individual foci of multicentric/multifocal breast cancer using targeted next generation sequencing
Dataset
EGAD00001000624
-
Assessment of genetic and epigenetic variation in human IPS cells
Dataset
EGAD00001000798
-
Genetic drivers of epigenetic and transcriptional variation of human immune responses to infection (RNA-seq, ATAC-seq and ChIPmentation)
Dataset
EGAD00001008422
-
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
-
Raw data for "Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse"
Dataset
EGAD00001010260
-
Genetic landscape of Extranodal NK/T-cell lymphoma
Dataset
EGAD00001009852
-
GILD-ExomeSeq-PTNHL
Dataset
EGAD00001001986
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Dataset
EGAD00001002266
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Dataset
EGAD00001001596
-
BASIS BC WGS Dataset
Dataset
EGAD00001001337
-
RNA-seq of Liver Cancer
Dataset
EGAD00001003993
-
WGoxBS and SureSelect data of the POPS placenta samples
Dataset
EGAD00001003136
-
Genetics of gene expression in human macrophage response to Salmonella
Dataset
EGAD00001003204
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Dataset
EGAD00001003409
-
Cooperative activity of BRAF F595L and mutant HRAS in histiocytic sarcoma provides new insights into oncogenic BRAF signaling
Dataset
EGAD00001001384
-
High-powered complex trait association mapping through whole genome sequencing of a selected subpopulation of the INGI-Val Borbera genetic isolate
Dataset
EGAD00001000730
-
Whole genome sequence of third generation family member (SFHS)
Dataset
EGAD00001001454
-
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
-
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
-
Whole genome sequencing in 1038 index cases reveals novel causative genes in pulmonary arterial hypertension
Dataset
EGAD00001003423
-
Epigenome maps of time-resolved monocyte to macrophage differentiation and innate immune memory
Dataset
EGAD00001002693
-
Whole-exome sequencing of 20 samples of actinic keratosis (10s) and cutaneous squamous cell carcinoma (10s)
Dataset
EGAD00001003765
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Dataset
EGAD00001004286
-
Congenital anosmia 1
Dataset
EGAD00001002210
-
Sequencing data for ICGC Oesophageal Adenocarcinoma tissue samples - 129_rnaseq
Dataset
EGAD00001002260
-
The molecular landscape of colorectal cancer reveals genetic mutations(5 cases)
Dataset
EGAD00001003223
-
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
-
Comprehensive cancer predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes
Dataset
EGAD00001004088
-
Chromosome Segregation Errors Promote a Diverse Spectrum of Simple and Complex Genomic Rearrangements
Dataset
EGAD00001004163
-
Investigation of mutational signatures associated with DNMT3A deficiency (2019-04-03)
Dataset
EGAD00001004889
-
TRACERx100 metastatic samples
Dataset
EGAD00001003301
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Dataset
EGAD00001004157
-
IBD Whole Genome Sequencing Phase 1 (2018-08-03)
Dataset
EGAD00001004272
-
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
-
Exome sequencing of patients with rare neurological disorders
Dataset
EGAD00001000346
-
Congenital Heart Disease in UK Families
Dataset
EGAD00001000343
-
ENU-NCI-H508-Cetuximab-SecondRound
Dataset
EGAD00001002065
-
Open Targets 020 Epigenomes of Cell Lines (2018-10-23)
Dataset
EGAD00001004415
-
A study of the molecular pathogenesis of Splenic Marginal Zone and Diffuse Large B-Cell Lymphoma
Dataset
EGAD00001000410