Whole-genome sequencing in gastric cancer (part2)

Study ID Alternative Stable ID Type
EGAS00001006575 Other

Study Description

we analysis structural variations (SVs) and mutational signatures via whole-genome sequencing of 168 GCs. Our data demonstrates diverse models of complex SVs operative in GC, which lead to high-level amplification of oncogenes. We find varying proportion of tandem-duplications (TDs) among individuals and identify 24 TD hotspots involving well-established cancer genes such as CCND1, ERBB2 and MYC.

Study Datasets 1 dataset.

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Dataset ID Description Technology Samples
whole-genome sequencing data of 177 samples.
HiSeq X Ten 177

Who archives the data?

There are no publications available