-
Single cell TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008161
-
OMKar
Study
EGAS00001008245
-
Peruvian Population Genomics: Unraveling the Genetic Landscape and Admixture Dynamics of Urban Populations
Study
EGAS00001008264
-
Genome-wide methylation detection and episignature analysis using PacBio long-read sequencing
Study
EGAS00001008250
-
Cell of Origin and Early Evolution of Leukemia in Down Syndrome
Dataset
EGAD00001006555
-
Paired-WGS-two-families-with-GBA-variants-and-Parkinsons-disease
Dataset
EGAD00001006561
-
Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial
Dataset
EGAD00001006585
-
BC WGS Dataset
Dataset
EGAD00001001338
-
Triple Negative BC RNA Sequencing
Dataset
EGAD00001001339
-
Breast RNA Sequencing
Dataset
EGAD00001001340
-
BASIS RNA Sequencing
Dataset
EGAD00001001341
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Dataset
EGAD00001001356
-
Neuroblastoma relapse trio series from the AMC
Dataset
EGAD00001001360
-
Egypt Genome Project - low coverage whole genome sequencing
Dataset
EGAD00001001372
-
Mechanisms of patient response to Dabrafenib in Melanoma
Dataset
EGAD00001001375
-
Egypt Genome Project - high coverage whole genome sequencing
Dataset
EGAD00001001380
-
Cooperative activity of BRAF F595L and mutant HRAS in histiocytic sarcoma provides new insights into oncogenic BRAF signaling
Dataset
EGAD00001001384
-
Understanding population genetics and patterns of genome-wide heterozygosity in a sample of the Croatian isolated populations (ESGIDalmatians)
Dataset
EGAD00001001387
-
Skin Adenocarcinoma Genome Sequencing
Dataset
EGAD00001001100
-
Subclonal diversification of primary breast cancer
Dataset
EGAD00001000965
-
Harnessing transposons for drug resistance gene discovery in cancer
Dataset
EGAD00001000980
-
Multi-omics analysis defines core genomic alterationsin pheochromocytomas and paragangliomas
Dataset
EGAD00001000986
-
BLUEPRINT: Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Dataset
EGAD00001001011
-
Whole Exome Sequencing of healthy Spanish individuals - Fastq files
Dataset
EGAD00001001012
-
Autozygosity pilot - British-Pakistani from Birmingham
Dataset
EGAD00001001025
-
Autozygosity pilot - British-Pakistani from Birmingham 2
Dataset
EGAD00001001026
-
Genetic background for the major psychiatric disorders in the general Finnish population
Dataset
EGAD00001001250
-
Genetic background for cardio vascular disorders in the general Finnish population
Dataset
EGAD00001001251
-
BASIS RNAseq
Dataset
EGAD00001001264
-
ESGI-Exome sequencing in Circulating Tumor Cells to determine therapy related markers
Dataset
EGAD00001001425
-
TGS - Comprehensive Molecular Characterization of Colorectal Cancer Metastases (2015-07-02)[MOSAIC]
Dataset
EGAD00001001426
-
SCLC study Peifer et al. - RNAseq dataset
Dataset
EGAD00001001431
-
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Dataset
EGAD00001001441
-
Atypical teratoid/rhabdoid tumors (ATRT) are comprised of three epigenetic subgroups with distinct enhancer landscapes
Dataset
EGAD00001001444
-
Whole genome sequence of third generation family member (SFHS)
Dataset
EGAD00001001454
-
Autozygosity pilot - QMUL
Dataset
EGAD00001001027
-
Whole Exome Sequencing files accompanying Genetic landscape of pediatric Rhabdomyosarcoma
Dataset
EGAD00001001059
-
Autozygosity pilot - Born in Bradford (2014-11-20)
Dataset
EGAD00001001079
-
PKD1 capture-by-hybridization resequencing for genetic diagnostics of polycystic kidney disease
Dataset
EGAD00001001091
-
Her2 BC WGS dataset
Dataset
EGAD00001001334
-
Triple Negative BC WGS Dataset
Dataset
EGAD00001001335
-
Xenograft BC WGS Dataset
Dataset
EGAD00001001336
-
BASIS BC WGS Dataset
Dataset
EGAD00001001337
-
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
-
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 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
-
GILD-ExomeSeq-PTNHL
Dataset
EGAD00001001986
-
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
-
Non-ADT METs ICGC Prostate UK
Dataset
EGAD00001002002
-
Ashkenazi Jewish Leukoencephalopathy Syndrome
Dataset
EGAD00001002005
-
Characterisation of the genomic landscape of CRLF2-d ALL
Dataset
EGAD00001002007
-
Characterisation of the genomic landscape of CRLF2-d ALL
Dataset
EGAD00001002008
-
Low-depth whole genome sequencing across multiple isolated populations
Dataset
EGAD00001002014
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Dataset
EGAD00001001596
-
Sequence Data for Paper: Epigenetic reprogramming during differentiation of human CD4+ T lymphocytes into memory stages
Dataset
EGAD00001001865
-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Dataset
EGAD00001001871
-
Solid_WXS_BL
Dataset
EGAD00001002104
-
Solid_WXS_MET
Dataset
EGAD00001002105
-
Solid_WXS_MET-XEN
Dataset
EGAD00001002106
-
Solid_WXS_T
Dataset
EGAD00001002107
-
Chromatin accessibility maps of chronic lymphocytic leukemia identify subtype-specific epigenome signatures and transcription regulatory networks
Dataset
EGAD00001002110
-
ENU-CCK-81 cetuximab pilot project
Dataset
EGAD00001001947
-
ENU-NCI-H508 cetuximab fixed concentration project
Dataset
EGAD00001001948
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS)
Dataset
EGAD00001001901
-
Genetic screening of GPI-anchor protein synthesis
Dataset
EGAD00001001928
-
Somatic Genetics of lesions from a POT1 patient (2016-04-20)
Dataset
EGAD00001002050
-
ENU-NCI-H508-Cetuximab-SecondRound
Dataset
EGAD00001002065
-
Single nucleus ATAC sequencing of isolated NK cells and CD56+ T cells from digested NSCLC tumor lesions
Study
EGAS50000001190
-
Expanding CIRdb, a comprehensive catalog of whole-exome sequencing data of Canary Islanders
Study
EGAS50000001726
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Dataset
EGAD00001001662
-
Low coverage whole-genome sequencing of samples from the Cretan Greek isolate collection HELIC-MANOLIS
Dataset
EGAD00001001637
-
Triple Negative Breast Cancer Whole Genome Validations
Dataset
EGAD00001000662
-
The Natural History of Human Prostate Cancer
Dataset
EGAD00001000689
-
Whole genome sequencing of an individual's genomic DNA and that of its lymphoblastoid cell line.
Dataset
EGAD00001000693
-
Sequencing probands and families with severe insulin resistance syndromes
Dataset
EGAD00001000694
-
SCLC study Peifer et al. - WES dataset
Dataset
EGAD00001000703
-
Whole genome sequencing of Italian genetic isolates -Friuli Venezia Giulia
Dataset
EGAD00001000728
-
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 sequencing of individuals from Val Borbera, Italy
Dataset
EGAD00001000731
-
RRBS data of 48 individuals of the Dutch Hunger Winter Families Study
Dataset
EGAD00001000733
-
Balanced Brain Tumour Whole Genome Sequencing
Dataset
EGAD00001000369
-
Assessment of genetic and epigenetic variation in human IPS cells
Dataset
EGAD00001000384
-
Triple Negative Breast Cancer RNA Sequencing
Dataset
EGAD00001000390
-
Sequencing component for the whole genome methylation analysis in PBMCs and cell subsets (pilot study)
Dataset
EGAD00001000394
-
Next Generation Sequencing in an IBD Pedigree Whole Genome Data
Dataset
EGAD00001000399
-
Genetic factors underlying premature coronary heart disease in patients with normal coronary arteries
Dataset
EGAD00001000402
-
ENGAGE - Amendment "500 genes exon sequencing"
Dataset
EGAD00001000403
-
A study of the genetic basis of evation by Acute Myeloid Leukaemia of Graft vs Leukaemia effects after allogeneic bone marrow transplantation
Dataset
EGAD00001000404
-
Paroxysmal Neurological Disorders 2
Dataset
EGAD00001000407
-
Whole-exome sequencing of rare autoimmune-related phenotypes
Dataset
EGAD00001000408
-
Identification of low frequency variants associated with ulcerative colitis using whole-genome sequencing
Dataset
EGAD00001000409
-
A study of the molecular pathogenesis of Splenic Marginal Zone and Diffuse Large B-Cell Lymphoma
Dataset
EGAD00001000410
-
Paroxysmal neurological Disorders
Dataset
EGAD00001000412
-
Osteosarcoma RNAseq
Dataset
EGAD00001000826
-
Assessment of epigenetic variation in human iPS cells-Medip
Dataset
EGAD00001000827
-
Role of Epigenetic Memory in Human Induced Pluripotent Stem Cells Pilot
Dataset
EGAD00001000828
-
FinHer Breast Cancer Study
Dataset
EGAD00001000871
-
RNA-Seq files accompanying Genetic landscape of pediatric Rhabdomyosarcoma
Dataset
EGAD00001000878
-
Exome sequencing of serially transplanted genetically marked IC-enriched primary PDAC cultures.
Dataset
EGAD00001000884