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Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Dataset
EGAD00001007736
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Dataset
EGAD00001010103
-
NSCLC WGS
Dataset
EGAD00001000888
-
Somatic mutation and clonal evolution normal breast tissue WGS
Dataset
EGAD00001010123
-
February 2020 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
EGAD00001006220
-
HV31 - Oxford Nanopore PromethION long-read sequencing
Dataset
EGAD00001007043
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data)
Dataset
EGAD00001010274
-
Duplexseq of the interstrand crosslinks_WGS
Dataset
EGAD00001010298
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Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - WGS
Dataset
EGAD00001010872
-
Sequence Data for Paper: Epigenetic reprogramming during differentiation of human CD4+ T lymphocytes into memory stages
Dataset
EGAD00001001865
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010913
-
Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
PSCP_bisulphite analysis in hESCs (2018-08-13)
Dataset
EGAD00001004295
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (ChIP-Seq for CD4-positive, alpha-beta T cell, on genome GRCh37)
Dataset
EGAD00001002673
-
August 2020 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
EGAD00001006383
-
Pre-clinical evolution of haematological malignancies_TGS
Dataset
EGAD00001006424
-
ENU-CCK-81 cetuximab pilot project
Dataset
EGAD00001001947
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma RNA
Dataset
EGAD00001014788
-
Paired-WGS-two-families-with-GBA-variants-and-Parkinsons-disease
Dataset
EGAD00001006561
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Dataset
EGAD00001007792
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma RNA
Dataset
EGAD00001014790
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia
Dataset
EGAD00001009304
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006643
-
Risk alleles of membranous nephropathy and recurrence of the disease on the grafted kidney
Dataset
EGAD00001007831
-
Solve-RD multi-omics data chud-faivre cohort
Dataset
EGAD00001015811
-
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
-
Resequencing candidate genes for male spermatogenic impairment
Dataset
EGAD00001006784
-
Solid_WXS_MET
Dataset
EGAD00001002105
-
Whole genome sequencing of Xeroderma Pigmentosum leukemias samples
Dataset
EGAD00001006322
-
HELIUS cohort gut microbiome batch2
Dataset
EGAD00001009732
-
Exome sequencing of UK Birth Cohorts - Millennium Cohort Study
Dataset
EGAD00001015372
-
Udated data for October 2017 data release 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
EGAD00001003906
-
Exome Sequencing of 44 subjects with very severe or fatal COVID-19
Dataset
EGAD00001008993
-
Anthropological dataset 1 for The admixture histories of Cabo Verde
Dataset
EGAD00001008976
-
Fine-mapping clustered GWAS hits enhances the identification of disease risk and protective genetic variants
Dataset
EGAD00001006916
-
Selection of somatic escape variants in SERPINA1 in liver tissue of patients with alpha-1 anti-trypsin deficiency - WGS
Dataset
EGAD00001015430
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
Autozygosity pilot - Born in Bradford (2017-05-11)
Dataset
EGAD00001003329
-
IfGH-10772
Dataset
EGAD00001003328
-
Whole genome sequencing of retinoblastoma reveals the diversity of rearrangements disrupting RB1 and uncovers a treatment related mutational signature
Dataset
EGAD00001006431
-
MutWP4: CRUK Grand Challenge Mutographs of Cancer: Pancreatic Organoids (2021-02-02)
Dataset
EGAD00001006933
-
Single cell transcriptional evolution of myeloid leukaemia of Down syndrome – scRNA
Dataset
EGAD00001015452
-
Genetic regulation of RNA splicing in human pancreatic islets
Dataset
EGAD00001009102
-
STAT1 AM RNAseq
Dataset
EGAD00001006962
-
Genetic drivers of epigenetic and transcriptional variation of human immune responses to infection (WGS and WGBS)
Dataset
EGAD00001008359
-
BLUEPRINT: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cells (WGS)
Dataset
EGAD00001002663
-
Somatic Genetics of lesions from a POT1 patient (2017-04-27)
Dataset
EGAD00001003307
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015477
-
Anthropological dataset 2 for The admixture histories of Cabo Verde
Dataset
EGAD00001008977