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Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients
Study
EGAS00001003563
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Effect of 28-day administration of Urolithin A to sedentary elderly on muscle gene expression
Study
EGAS00001003638
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single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes
Study
EGAS00001004070
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Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
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A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE
Study
EGAS00001007033
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'IL-17A-Producing ILC3s and Duodenal Adenoma in FAP'
Study
EGAS00001007347
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RNA sequencing on intestinal biopsies from inflammatory bowel disease patients treated with vehicle control, MEK inhibitor, or infliximab
Study
EGAS00001007534
-
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
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NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Study
EGAS00001007703
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Clonal tracing with somatic epimutations reveals dynamics of blood aging
Study
EGAS00001008056
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Assessing the suitability of formalin-fixed paraffin-embedded (FFPE) tissue for genome-wide association studies (GWAS)
Study
EGAS00001008103
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minION fastq files of 10 different tumor samples from the Master program (H021)
Dataset
EGAD00001008970
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Molecular profiling of tissue autopsies and ctDNA
Dataset
EGAD00001007040
-
Somatic mutations and single cell transcriptomes reveal the root of malignant rhabdoid tumours
Dataset
EGAD00001006296
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The transition from quiescent to activated states in human hematopoietic stem cells is governed by dynamic 3D genome reorganization
Dataset
EGAD00001006447
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RNA-seq data
Dataset
EGAD00001008128
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WES dataset of 20 pre-post paired neoadjuvant chemotherapy treated breast cancer samples
Dataset
EGAD00001008442
-
Molecular characterization of NASH-HCC
Dataset
EGAD00001007524
-
Multi-region sequencing of RCC with VTT and metastasis using WES and RNAseq
Dataset
EGAD00001008441
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Dataset
EGAD00001007872
-
Solve RD data - Short-Read Whole-Genome Sequencing, raw data, tuh-kounap_group samples
Dataset
EGAD00001015514
-
Adult B-precursor acute lymphoblastic leukemia transcriptomes
Dataset
EGAD00001008633
-
Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium
Dataset
EGAD00001002738
-
Spatially confined sub-tumor microenvironments in pancreatic cancer
Dataset
EGAD00001008155
-
Single-cell transcriptome of T-ALL P1
Dataset
EGAD00001008325
-
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
-
Dataset for hepatopancreaticobiliary_malignancy-RNA
Dataset
EGAD00001008863
-
WGS and WTS data of patient diagnosed with HSTCL
Dataset
EGAD00001005229
-
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
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Colorectal_LCM (2020-02-20)
Dataset
EGAD00001005994
-
Whole-genome sequencing of high-grade serous ovarian cancer (HGSC) tumours and matched normals from long-term survivors.
Dataset
EGAD00001009398
-
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
-
Deciphering the genomic, epigenomic and transcriptomic landscapes of pre-invasive lung cancer lesions to determine prognosis
Dataset
EGAD00001003883
-
Whole transcriptome RNA sequencing on bone marrow and peripheral blood samples from patients with acute myeloid leukemia at diagnosis or relapse.
Dataset
EGAD00001004187
-
Spatial heterogeneity of follicular lymphoma
Dataset
EGAD00001003553
-
GCT WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003267
-
CCOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003265
-
Identification of cardiovascular biomarkers through an integrative omics approach
Dataset
EGAD00001002197
-
GoNL aligned sequence data in BAM format.
Dataset
EGAD00001001038
-
RNA sequencing of periprostatic fat after a 6 month deep androgen deprivation therapy
Dataset
EGAD00001004971
-
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Dataset
EGAD00001005035
-
Exome trios in patients with gastroschisis (2019-04-08)
Dataset
EGAD00001004942
-
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
-
Exome sequencing of UK Birth Cohorts - Avon Longitudinal Study of Parents and Children
Dataset
EGAD00001015371
-
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