Data provider Accession Acronym URL
EGAO00000000035

This data provider is associated with 99 studies:

Study Accession Titlesort descending
EGAS00001000724 100 TUMOURS - To deeply sequence tumour and normal genomic DNA (including the precursor condition Barrett’s esophagus when material is available) to provide a comprehensive catalogue of somatic mutations - This study contains tumour samples from a cohort of 100 patients.
EGAS00001002331 160 WES and 25 WGS for HBV related HCC, and 15 WES for ICC belongs LICA-CN.
EGAS00001000170 20 Matched Pair Breast Cancer Genomes
EGAS00001001178 560 whole-genome sequenced breast cancers
EGAS00001001475 71 Whole-exome sequencing of Esophageal Squamous Cell Carcinoma on Chinese Patients
EGAS00001001539 A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
EGAS00001002091 A new subgroup of hepatocellular adenomas with sonic hedgehog pathway activation
EGAS00001001155 Anaplastic Meningioma V3 cancer gene panel
EGAS00001000174 Balanced Ependymoma
EGAS00001001520 BAP1 sequence of uveal melanoma cell lines
EGAS00001000726 BARRETT'S - To deeply sequence tumour and normal genomic DNA (including the precursor condition Barrett’s esophagus when material is available) to provide a comprehensive catalogue of somatic mutations - This study contains Barrett's oesophagus samples
EGAS00001001431 Breast Cancer - Subtype defined by an amplification of the HER2 gene
EGAS00001001908 Breast Cancer - Very young women
EGAS00001000211 Breast Cancer Exome Sequencing
EGAS00001000166 Breast Cancer Matched Pair Cell Line Whole Genomes

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