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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
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
-
Beacon v2 and Federated EGA, part of the GDI project Starter Kit to enable access to genomic and phenotypic data across borders
Blog
beacon-v2-and-federated-ega-part-of-the-gdi-project-starter-kit