-
Genome and transcriptome sequence data from a transformed diffuse large B cell lymphoma patient
Dataset
EGAD00001005869
-
Genome and transcriptome sequence data from a chordoma patient
Dataset
EGAD00001005871
-
Genome and transcriptome sequence data from a breast carcinoma patient
Dataset
EGAD00001005888
-
Genome and transcriptome sequence data from a thyroid hurthle cell carcinoma patient
Dataset
EGAD00001005891
-
Genome and transcriptome sequence data from a metastatic gallbladder adenocarcinoma patient
Dataset
EGAD00001005903
-
Colorectal_organoids_and_tumour_tissue___Whole_Genome_X10
Study
EGAS00001001100
-
Angiopredict: predicting response for bevacizumab treatment
Study
EGAS00001002724
-
Shallow-whole genome sequencing for copy numbers in resectable gastric cancer treated with surgery alone
Dataset
EGAD00001011994
-
Characterising the evolutionary dynamics of cancer proliferation in single-cell clones with SPRINTER
Dataset
EGAD00001015411
-
Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
Study
EGAS00001007383
-
Efficacy of nivolumab in pediatric cancers with high mutation burden and mismatch-repair deficiency
Study
EGAS00001007393
-
Seq-ing the SINEs of Central Nervous System Tumors in Cerebrospinal Fluid
Study
EGAS00001007401
-
Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths
Study
EGAS00001007402
-
Genomic and anti-tumor immune evolution of breast cancer
Study
EGAS00001004956
-
WES of Colorectal cancer organoid-stroma biobank cohort
Study
EGAS00001007301
-
Single-cell roadmap of immune cell responses in chronic myeloid leukemia
Study
EGAS00001005044
-
mutational landscape of normal human breast
Study
EGAS00001004672
-
Epithelioid haemangioendothelioma (EHE) case series from the Stafford Fox Rare Cancer Program
Study
EGAS00001007474
-
Study of the microenvironment of angioimmunoblastic T-cell lymphoma
Study
EGAS00001006401
-
Sequencing of Breast Cancer
Study
EGAS00001007490
-
Sequencing of Ovarian Cancer
Study
EGAS00001007489
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Study
EGAS00001005736
-
Mutant p53 confers gain-of-function transcriptional activity in liver cancer
Study
EGAS00001005779
-
Single cell Transcriptomic Analysis of Cellular Heterogeneity in Human Colorectal Tumors
Study
EGAS00001001945
-
Unraveling the genetics of transformed splenic marginal zone lymphoma
Study
EGAS00001006389
-
Evolutionary histories of breast cancer and related clones
Study
EGAS00001006282
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
Genomic profiling of subcutaneous patient derived xenograft models of solid childhood cancer
Study
EGAS00001006710
-
Leukemia sequencing study
Study
EGAS00001006901
-
IACS treatment on breast cancer bone metastases
Study
EGAS00001006908
-
A capture-based next-generation sequencing panel for the molecular characterization of chronic lymphocytic leukemia
Study
EGAS00001006975
-
Targeted sequence of MDS cases treated with azacitidine
Study
EGAS00001007030
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Study
EGAS00001002725
-
Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin
Study
EGAS00001006879
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma
Study
EGAS00001007172
-
an integrated molecular study of clear cell renal cell carcinoma (ccRCC) including whole-genome/exome and RNA sequencing as well as array-based gene expression/copy-number/methylation analyses
Study
EGAS00001000509
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Tumor-intrinsic expression of the autophagy gene Atg16l1 suppresses anti-tumor immunity in colorectal cancer
Study
EGAS00001005952
-
Detection of rare mutations, copy number variation, and DNA methylation in the same template DNA molecules
Study
EGAS00001006839
-
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
-
Single-cell profiling maps the spectrum of crosstalk between glioma cells and tumor associated macrophages
Study
EGAS00001002185
-
Molecular Classification of Lymph Node Metastases Subtypes Predict for Survival in Head and Neck Cancer
Study
EGAS00001003233
-
Genomic and transcriptomic landscape of aggressive thyroid cancer
Study
EGAS00001003540
-
Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Study
EGAS00001004013
-
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Study
EGAS00001005230
-
The INFORM Precision Medicine Study for High-Risk Pediatric Malignancies
Study
EGAS00001005112
-
Single-cell profiling of neoantigen-specific T cells in lung cancers treated with neoadjuvant PD-1 blockade
Study
EGAS00001005343
-
RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors
Study
EGAS00001005588
-
Genome analysis of early onset sporadic rectal cancer
Study
EGAS00001005970
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (RNA-seq)
Study
EGAS00001006016
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq)
Study
EGAS00001006017
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations
Study
EGAS00001006034
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - WGS data
Study
EGAS00001006610
-
Palbociclib resistance analyses on breast cancer bone metastasis PDX
Study
EGAS00001006428
-
Analyses of IACS-010759 treatment resistance on breast cancer bone metastases
Study
EGAS00001006429
-
Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Study
EGAS00001006598
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations - Cancer Panel data
Study
EGAS00001006642
-
Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in HGSOC
Study
EGAS00001006807
-
Diet driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome
Study
EGAS00001006982
-
Molecular features of adenomas predicting metachronous colorectal cancer: a nested-case control study
Study
EGAS00001007039
-
Submission 10 - study_title 2
Study
EGAS50000000073
-
Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project
Study
EGAS00001000381
-
Genetic landscape of pediatric Rhabdomyosarcoma
Study
EGAS00001000256
-
Cell_lines_with_telomere_fusion_induced_rearrangements
Study
EGAS00001001059
-
Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma
Study
EGAS00001004843
-
Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib
Study
EGAS00001004666
-
UROMOL 2020 - RNA-seq data
Study
EGAS00001004693
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
High-grade serous ovarian cancer refined with single-cell RNA-sequencing
Study
EGAS00001004987
-
Early ctDNA molecular response captures therapeutic response in the first stage of CCTG BR.36 ctDNA-directed, multi-center phase II study of molecular response adaptive immunotherapy in non-small cell lung cancer
Study
EGAS00001007298
-
Genetic landscape of pediatric Osteosarcoma
Study
EGAS00001000263
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
Oesophageal_Adenocarcinoma_Organoid_ATAC
Study
EGAS00001003890
-
RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Study
EGAS00001000610
-
SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Study
EGAS00001007590
-
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Study
EGAS00001000932
-
Single-cell RNA sequencing of 22 Hodgkin lymphoma tumors and 5 reactive lymph nodes
Study
EGAS00001004085
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification (H021)
Study
EGAS00001006706
-
Integrated genetic analysis of primary CNS lymphoma
Study
EGAS00001007222
-
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Study
EGAS00001007327
-
Patient-derived organoids identify tailored therapeutic options and determinants of plasticity in sarcomatoid urothelial bladder cancer
Study
EGAS00001007430
-
Genentech Small Cell Lung Cancer (SCLC) Screen
Study
EGAS00001000334
-
Single cell RNA sequencing of normal endometrial derived organoids uncovers novel cell type markers for prognostication
Study
EGAS00001004466
-
Drug-perturbation-based stratification of blood cancer
Study
EGAS00001001746
-
Kidney_tumour_RNA
Study
EGAS00001002487
-
Orphan_Tumour_Study___RNAseq
Study
EGAS00001002534
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Oncogenic Ectodomain deletion of FGFR1 caused by Breakage-Fusion-Bridges in Squamous Cell lung Cancer
Study
EGAS00001005059
-
Oesophageal_Adenocarcinoma_Organoid_10x
Study
EGAS00001003191
-
The genomic landscape of pediatric acute lymphoblastic leukemia
Study
EGAS00001005250
-
One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Study
EGAS00001006886
-
The genomic imprint of cancer therapies helps timing the formation of metastases
Study
EGAS00001003416
-
The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer
Study
EGAS00001007086
-
RNA-Sequencing data of patient derived normal fibroblasts (NFs), cancer associated fibroblasts (CAFs) and tumor spheroid samples
Study
EGAS00001007205
-
RNAseq
Study
EGAS00001007212
-
TNBC ctDNA Targeted Panel
Study
EGAS00001006937