-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
Genomic and immune profiling of pre-invasive lung adenocarcinoma
Study
EGAS00001004006
-
H3Africa - Respiratory Microbiota of African Children
Study
EGAS00001004401
-
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
-
Single-cell proteo-genomic reference maps of the human hematopoietic system
Study
EGAS00001005593
-
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Study
EGAS00001006565
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Genome-wide mutation analysis of germinal-center B-cell derived lymphomas within the ICGC MMML-Seq Consortium
Study
EGAS00001000394
-
DPY30_ChIP_seq
Study
EGAS00001001132
-
GM adipose tissue study
Study
EGAS00001007126
-
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Study
EGAS00001000599
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
Genomic landscape of Ewing sarcoma (ICGC project)
Study
EGAS00001000855
-
RNA-seq study of longitudinal blood cell samples from children at risk of type 1 diabetes
Study
EGAS00001004071
-
Genomic characterization of hepatocellular carcinoma in Hispanic patients
Study
EGAS00001007431
-
Papuan Genomes: whole genome sequencing
Study
EGAS00001001247
-
Cell motility and migration as determinants of stem cell efficacy
Study
EGAS00001002478
-
Targeting PTPRK-RSPO3 colon tumours promotesdifferentiation and loss of stem-cell function
Study
EGAS00001001462
-
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
-
A dataset compiled as a resource a for orthogonal assessment of exon CNV calling in NGS data
Study
EGAS00001002428
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie
Study
EGAS00001002506
-
Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected
Study
EGAS00001000769
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
Integrative_Oncogenomics_of_multiple_myeloma
Study
EGAS00001000244
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
Whole Exome Sequencing in Multiple Myeloma
Study
EGAS00001003227
-
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Study
EGAS00001000958
-
Exome sequencing of 1000 population control samples from the UK 1958 birth cohort
Study
EGAS00001000971
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
-
Pilot_experiment_on_functional_genomics_in_osteoarthritis_RNA
Study
EGAS00001001203
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability
Study
EGAS00001003572
-
Integrated Genomic Analysis of Chronic Lymphocytic Leukaemia
Study
EGAS00001001306
-
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
-
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
-
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Study
EGAS00001005322
-
Mutational_landscape_in_haemochromatosis__exome_
Study
EGAS00001005158
-
Genome Asia 100K Project
Study
EGAS00001002921
-
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Study
EGAS00001004064
-
Targeted deep sequencing on Pediatric MDS
Study
EGAS00001005431
-
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
-
'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
-
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
-
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
-
minION fastq files of 10 different tumor samples from the Master program (H021)
Dataset
EGAD00001008970
-
Molecular profiling of tissue autopsies and ctDNA
Dataset
EGAD00001007040
-
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
-
RNA-seq data
Dataset
EGAD00001008128
-
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