-
The function of circular RMST in neuroendocrine tumours
Study
EGAS50000000897
-
Labcorp® Plasma Detect™ assay: whole genome sequencing analyses of plasma cfDNA, white blood cells and FFPE tumor tissue
Dataset
EGAD50000001180
-
Whole genome sequencing to identify structural variants in early-stage breast cancer
Dac
EGAC50000000461
-
WES dataset
Dataset
EGAD50000001164
-
Clinical validity of post-surgery circulating tumor DNA (ctDNA) in stage III colon cancer patients treated with adjuvant chemotherapy: the PROVENC3 study
Study
EGAS50000000804
-
Multimodal plasma and urinary cell-free DNA profiling improves risk stratification in newly diagnosed prostate cancer
Study
EGAS00001008195
-
SCANDARE TNBC
Study
EGAS50000000970
-
Primary breast tumor heterogeneity through therapy
Study
EGAS00001003168
-
CAGEKID: Cancer Genomics of the Kidney
Study
EGAS00001000083
-
Recurrent somatic DICER1 mutations in non-epithelial ovarian tumors
Study
EGAS00001000135
-
Full genome sequencing of a monozygotic twin discordant for schizophrenia
Study
EGAS00001000152
-
Whole genome sequencing of matched primary and metastatic acral melanomas
Study
EGAS00001000169
-
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Study
EGAS00001000226
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00001000245
-
Accurate mutation detection in leukemia by re-sequencing a cancer gene set
Study
EGAS00001000268
-
Genentech Colon Cancer Screen
Study
EGAS00001000288
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Inferring tumor genomes from peripheral blood i.e. CTCs and plasma-DNA using deep sequencing and targeted enrichment
Study
EGAS00001000337
-
Genetic landscape of pediatric Retinoblastoma
Study
EGAS00001000346
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Study
EGAS00001000370
-
The genomic landscape of large and small tumors in early-onset prostate cancer patients
Study
EGAS00001000383
-
The landscape of somatic mutations in epigenetic regulators across 1000 pediatric cancer genomes
Study
EGAS00001000449
-
Identification of mutations and structural rearrangements in plasma DNA form metastatic prostate cancer patients
Study
EGAS00001000453
-
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
-
A Cancer Cell-Line Titration Series for Evaluating Somatic Classification
Study
EGAS00001001016
-
Single cell sequencing of breast cancer T cells reveals a tissue-resident memory subset associated with improved prognosis
Study
EGAS00001002845
-
De novo metastatic prostate cancer cohort
Dataset
EGAD50000002381
-
Multifocal cohort analysis unveils cell types associated with regional lymph node seeding in prostate cancer
Study
EGAS00001006715
-
Locally advanced prostate cancer cohort
Dataset
EGAD50000002380
-
Data Access Committee for the DNA sequencing data included in the study "Multifocal cohort analysis unveils cell types associated with regional lymph node seeding in prostate cancer".
Dac
EGAC50000000930
-
Multiomic cell-free DNA profiling to inform molecular classification and immunotherapy outcomes in endometrial cancer
Study
EGAS50000001582
-
Biomodal duet +modC sequencing of endometrial cancer plasma cfDNA samples
Dataset
EGAD50000002261
-
TruSight Oncology 500 ctDNA targeted sequencing data from endometrial cancer patients
Dataset
EGAD50000002262
-
Whole-genome sequencing of endometrial cancer plasma circulating DNA
Dataset
EGAD50000002263
-
Variant calling for LUNG-NSCLC2 cohort
Dataset
EGAD50000002235
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 17)
Dataset
EGAD50000002409
-
High-depth whole genome sequencing of 51 premalignant breast lesions
Study
EGAS50000001436
-
High-depth whole genome sequencing of 26 premalignant breast lesions
Study
EGAS50000001559
-
High-depth whole genome sequencing of paired ductal carcinoma in-situ (DCIS) and germline control samples from 51 individuals.
Dataset
EGAD50000002071
-
High-depth whole genome sequencing of paired ductal carcinoma in-situ (DCIS) and germline control samples from 26 individuals.
Dataset
EGAD50000002237
-
DCIS fresh frozen fragmentomics dataset
Study
EGAS50000001475
-
Genomic and transcriptomic analysis of thymic epithelial tumors
Study
EGAS00001004227
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001585
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001598
-
Triple-negative breast cancer sequencing data
Dataset
EGAD50000002266
-
Triple-negative breast cancer - Visium HD data
Dataset
EGAD50000002284
-
Efficacy of dual KRAS G12D–EGFR blockade versus triple combinations in patient-derived models of KRAS G12D-mutant colorectal cancer
Study
EGAS50000001700
-
RNA sequencing of untreated and treated KRAS-mutated metastatic colorectal cancer PDX-derived organoids.
Dataset
EGAD50000002443
-
The evolutionary steps from primary to metastatic prostate cancer are largely uncharted, and the ability to use DNA present in body fluids as correlates of aggregate metastatic status is under-examined. We reconstructed phylogenies in ten prostate cancer patients with fatal disease using deep targeted sequencing of the prostate, adjacent and distant organs, as well as plasma, serum, and cerebrospinal fluid at various time points. A total of 163 samples are studied.
Study
EGAS00001003848
-
Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Study
EGAS00001003853
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Mutational signature in colorectal cancer induced by genotoxic pks+ E. coli
Study
EGAS00001003934
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
ER___HER2___PR__breast_Cancer_genome_sequencing
Study
EGAS00001000197
-
Melanoma_TIL_Study_Exomes
Study
EGAS00001000216
-
Adult granulosa cell tumor WGS data cohort with corresponding reference germline WGS data
Study
EGAS00001004249
-
Rapid response of APC/TP53/KRAS mutated stage IV colorectal cancer under FOLFIRI + Bevacizumab detected by liquid biopsy: a case report
Study
EGAS00001004088
-
Whole genome bisulfite sequencing of hepatitis B virus-associated hepatocellular carcinoma tumor and non-cancerous samples
Study
EGAS00001002230
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
FFPE_Normal_Panel_V3_Cancer_Panel
Study
EGAS00001000836
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Single-cell profiling maps the spectrum of crosstalk between glioma cells and tumor associated macrophages
Study
EGAS00001002185
-
Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients.
Study
EGAS00001005698
-
Myeloproliferative_Neoplasms__MPN__Exome_Validation_Study
Study
EGAS00001000404
-
The role of the mammalian SWI/SNF chromatin remodeling complex in neuroendocrine prostate cancer
Study
EGAS00001004177
-
Genentech Small Cell Lung Cancer (SCLC) Screen
Study
EGAS00001000334
-
Placental_mosaicism
Study
EGAS00001003549
-
Whole Exome sequencing of colorectal cancer patients (SG-BULK)
Study
EGAS00001006006
-
Tissue-specific cell-free DNA degradation quantifies circulating tumor DNA burden
Study
EGAS00001004657
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing
Study
EGAS00001004760
-
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Study
EGAS00001004940
-
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_
Study
EGAS00001001941
-
hereditary BrEAst Case CONtrol study
Study
EGAS00001005043
-
Whole-exome sequencing performed on a patient with chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia
Study
EGAS00001005117
-
Engineering large chromosomal deletions by CRISPR-Cas9
Study
EGAS00001005134
-
Mutational_landscape_in_haemochromatosis__WGS_
Study
EGAS00001005157
-
The genomic landscape of pediatric acute lymphoblastic leukemia
Study
EGAS00001005250
-
Comparison of capture-based method for transcriptome profiling of formalin-fixed paraffin embedded tumor samples
Study
EGAS00001005255
-
Whole-genome sequencing in gastric cancer (part2)
Study
EGAS00001006575
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
Multiple_myeloma_precursor_genomics
Study
EGAS00001006312
-
Myelodysplastic_Syndrome_Exome_Sequnecing
Study
EGAS00001000089
-
Chordoma_Exome_Sequencing
Study
EGAS00001000188
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Chordoma_Targeted_Sequencing_Study
Study
EGAS00001000280
-
Evaluation_of_size_selection_on_cancer_specific_sequencing_libraries
Study
EGAS00001000293
-
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
-
Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers
Study
EGAS00001005556
-
Metastatic_Breast_Cancer_Validation
Study
EGAS00001001968
-
DERMATLAS__Hidradenoma_papilliferum_WES
Study
EGAS00001005714
-
DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
-
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Extensive three-dimensional intratumor proteomic heterogeneity revealed by multiregion sampling in high-grade serous ovarian tumor specimens
Study
EGAS00001005786
-
SPECTA RP-1759-AYA Sarcoma cohort
Study
EGAS00001005840
-
Mesothelioma_Whole_Genomes
Study
EGAS00001000830
-
Sequencing of an organoid biobank for childhood soft tissue sarcoma.
Study
EGAS00001005912
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655