-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: pancreas (2019-04-03)
Dataset
EGAD00001004893
-
Small-molecule inhibitors in melanoma - Kenski / Kong - WES (2019-04-11)
Dataset
EGAD00001004952
-
Deciphering the genomic, epigenomic and transcriptomic landscapes of pre-invasive lung cancer lesions to determine prognosis
Dataset
EGAD00001003883
-
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Dataset
EGAD00001005035
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Colorectal_LCM (2020-02-20)
Dataset
EGAD00001005994
-
Somatic mutations and single cell transcriptomes reveal the root of malignant rhabdoid tumours
Dataset
EGAD00001006296
-
The transition from quiescent to activated states in human hematopoietic stem cells is governed by dynamic 3D genome reorganization
Dataset
EGAD00001006447
-
Identification of cardiovascular biomarkers through an integrative omics approach
Dataset
EGAD00001002197
-
Exploring germline and somatic mutagenesis in the extended family with germline pathogenic variant in POLD1
Study
EGAS00001006434
-
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Study
EGAS00001006565
-
Genomic characterization of hepatocellular carcinoma in Hispanic patients
Study
EGAS00001007431
-
GM adipose tissue study
Study
EGAS00001007126
-
Exploring the cell-free total RNA transcriptome in diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma patients as biomarker source in blood plasma liquid biopsies
Study
EGAS00001007585
-
RNA-seq study of longitudinal blood cell samples from children at risk of type 1 diabetes
Study
EGAS00001004071
-
Whole Exome Sequencing in Multiple Myeloma
Study
EGAS00001003227
-
Clinical activity and molecular correlates of response to atezolizumab alone or in combination with bevacizumab versus sunitinib in renal cell carcinoma
Study
EGAS00001002928
-
Cell motility and migration as determinants of stem cell efficacy
Study
EGAS00001002478
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
RNA-seq of cultured human hematopoietic stem and progenitor cells from umblical cord blood in cytokine-rich ex vivo culture conditions following sphingolipid modulation
Study
EGAS00001003756
-
Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
-
A dataset compiled as a resource a for orthogonal assessment of exon CNV calling in NGS data
Study
EGAS00001002428
-
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495
-
Genomic and immune profiling of pre-invasive lung adenocarcinoma
Study
EGAS00001004006
-
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie
Study
EGAS00001002506
-
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Study
EGAS00001005322
-
Mutational_landscape_in_haemochromatosis__WGS_
Study
EGAS00001005157
-
Single-cell profiling of the leukemic and non-leukemic immune cell compartments in CD8+ T-cell Large Granular Lymphocytic Leukemia
Study
EGAS00001005297
-
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Single-cell proteo-genomic reference maps of the human hematopoietic system
Study
EGAS00001005593
-
Prostate Cancer and Normal Adjacent Prostate RNA-seq samples, NGS-ProToCol
Study
EGAS00001002816
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
-
H3Africa - Respiratory Microbiota of African Children
Study
EGAS00001004401
-
Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability
Study
EGAS00001003572
-
PCa-LINES
Study
EGAS00001004613
-
16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer
Study
EGAS00001004624
-
Mitochondrial DNA mutations contribute to autism and also to the characteristics of mitochondrial disorders present in patients with autism spectrum disorders
Study
EGAS00001002750
-
Aberrant ERBB4-SRC Signaling as a Hallmark of Group 4 Medulloblastoma Revealed by Integrative Phosphoproteomic Profiling
Study
EGAS00001002757
-
Mutational_landscape_in_haemochromatosis__exome_
Study
EGAS00001005158
-
Genome Asia 100K Project
Study
EGAS00001002921
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Study
EGAS00001004064
-
Targeted deep sequencing on Pediatric MDS
Study
EGAS00001005431
-
Single-cell transcriptome of T-ALL P1
Dataset
EGAD00001008325
-
Temporal stability of circulating microRNAs in human serum
Study
EGAS00001003221
-
scRNA-seq of patient-derived PDAC organoids
Study
EGAS00001004661
-
STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma
Study
EGAS00001004719
-
Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer
Study
EGAS00001006040
-
The transcriptomic response of skeletal muscle in life-long high-level trained and untrained men and women after acute exercise
Study
EGAS00001006139
-
Clonal dominance defines metastatic dissemination in pancreatic cancer
Study
EGAS00001006358
-
Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients
Study
EGAS00001003563
-
Effect of 28-day administration of Urolithin A to sedentary elderly on muscle gene expression
Study
EGAS00001003638
-
single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes
Study
EGAS00001004070
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
-
A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE
Study
EGAS00001007033
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
-
'IL-17A-Producing ILC3s and Duodenal Adenoma in FAP'
Study
EGAS00001007347
-
RNA sequencing on intestinal biopsies from inflammatory bowel disease patients treated with vehicle control, MEK inhibitor, or infliximab
Study
EGAS00001007534
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Study
EGAS00001007703
-
Clonal tracing with somatic epimutations reveals dynamics of blood aging
Study
EGAS00001008056
-
Assessing the suitability of formalin-fixed paraffin-embedded (FFPE) tissue for genome-wide association studies (GWAS)
Study
EGAS00001008103
-
Molecular characterization of NASH-HCC
Dataset
EGAD00001007524
-
Spatially confined sub-tumor microenvironments in pancreatic cancer
Dataset
EGAD00001008155
-
minION fastq files of 10 different tumor samples from the Master program (H021)
Dataset
EGAD00001008970
-
WES dataset of 20 pre-post paired neoadjuvant chemotherapy treated breast cancer samples
Dataset
EGAD00001008442
-
RNA-seq data
Dataset
EGAD00001008128
-
Adult B-precursor acute lymphoblastic leukemia transcriptomes
Dataset
EGAD00001008633
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Exome sequencing of UK Birth Cohorts - Millennium Cohort Study
Dataset
EGAD00001015372
-
Multi-region sequencing of RCC with VTT and metastasis using WES and RNAseq
Dataset
EGAD00001008441
-
Dataset for hepatopancreaticobiliary_malignancy-RNA
Dataset
EGAD00001008863
-
May 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
EGAD00001008100
-
Whole-genome sequencing of high-grade serous ovarian cancer (HGSC) tumours and matched normals from long-term survivors.
Dataset
EGAD00001009398
-
Exome trios in patients with gastroschisis (2019-04-08)
Dataset
EGAD00001004942
-
Exome sequencing of UK Birth Cohorts - Avon Longitudinal Study of Parents and Children
Dataset
EGAD00001015371
-
The aim of this project is to identify, on 15 French Caucasian and 10 African-Caribbean men, through an integrative approach of DNA sequencing and transciptomic analyses, relevant genomic events that characterize or allow targeting the various phenotypes of aggressiveness of early stages of prostate cancer.
Study
EGAS00001002176
-
Combined – whole blood and skin fibroblasts - transcriptomic analysis in Psoriatic arthritis.
Study
EGAS00001006288
-
Peripheral blood DNA methylation of Crohn's disease patients starting treatment with adalimumab, vedolizumab or ustekinumab
Study
EGAS00001007532
-
Identifying autosomal recessive mutations causing neurological disorders
Study
EGAS00001000023
-
Recording physiological history of cells with chemical labeling.
Study
EGAS50000000056
-
Clonal heterogeneity leads to secondary resistance in a melanoma patient after adoptive cell therapy with tumor-infiltrating lymphocytes
Study
EGAS50000000279
-
Inferring causal genes at type 2 diabetes GWAS loci through chromosome interactions in islet cells
Dataset
EGAD50000000517
-
Genomic and clinical characterization of a familial GIST kindred intolerant to imatinib
Study
EGAS50000000372
-
Identification of germline variants in Medullary thyroid carcinoma (MTC) by whole- exome sequencing
Study
EGAS50000000061
-
Single cell multi-omics analysis of chromothriptic medulloblastoma highlights genomic and transcriptomic consequences of genome instability
Study
EGAS00001005410
-
Clinical relevance of TCGA subtypes for gastric cancer patients
Study
EGAS50000000779
-
10x genomics single cell RNA-seq and ATAC-seq from 10 pre-menopausal patients fimbriae and ampullary part of the fallopian tube
Study
EGAS50000000628
-
RNA-Seq of human longitudinal whole blood samples from PCR-positive and PCR-negative recent household contacts of COVID-19 index cases.
Study
EGAS50000000473
-
The function of circular RMST in neuroendocrine tumours
Study
EGAS50000000897
-
MATISSE bulk RNA-sequencing data
Dataset
EGAD50000001470
-
Transcriptomic profiling of circulating regulatory T cells from follicular lymphoma patients before and after Lenalidomide treatment
Study
EGAS50000001048
-
Nala TAS-LRS PGx Study
Dataset
EGAD50000001609
-
Head and neck tumor organoid biobank for modelling individual responses to radiation therapy according to the TP53/ HPV status
Study
EGAS50000001219
-
Ribosome profiling shows variable sensitivity to detect open reading frames for conventional and different types of cryptic T cell antigens
Study
EGAS50000000322
-
RNA sequencing data from glioblastoma primary cell lines treated with indisulam
Study
EGAS50000000680
-
Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk.
Dac
EGAC50000000169
-
An allele-resolved nanopore-guided tour of the human placental methylome
Study
EGAS50000001301
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Study
EGAS50000001327
-
Transcriptomic analysis of B-cell acute lymphoblastic leukaemia (B-ALL) patients treated on the ALL09 clinical trial
Study
EGAS50000001109
-
A single-cell multi-omic atlas of nodal B-cell non-Hodgkin lymphomas
Study
EGAS50000000342
-
Truncated FOS impairs osteogenic differentiation and induces prostaglandin and NFkB signalling in an in vitro cell-of-origin model for osteoid osteoma and osteoblastoma
Study
EGAS50000001291
-
ECM-free patient-derived organoids preserve diverse prostate cancer lineages and uncover in vitro-enriched cell types
Study
EGAS50000000807
-
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738
-
Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes
Study
EGAS00001000961
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Study
EGAS00001001973
-
Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma
Study
EGAS00001000554
-
MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition
Study
EGAS00001002115
-
Two lung cancer cell lines with EGFR mutations, PC-9 and KHM-3S, were either treated with Tarceva for 24 hours or left untreated. The gene expression profiles were examined by RNAseq, and the genome wide binding profiles of total STAT3 and pSTAT3 were characterized by ChIPseq.
Study
EGAS00001000793
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
ICGC Oesophageal adenocarcinoma - tumour samples
Study
EGAS00001000725
-
Spatio-temporal evolution of the primary glioblastoma genome
Study
EGAS00001001041
-
ICGC PedBrain: Deep-sequencing of childhood brain tumors.
Study
EGAS00001000215
-
Exome_sequencing_of_thyroid_disease_in_Val_Borbera
Study
EGAS00001000344
-
WGS of liver cancer in the Japanese population
Study
EGAS00001000678
-
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors
Study
EGAS00001000906