Study
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.
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00001009384 |
whole-genome sequencing data of 177 samples.
|
HiSeq X Ten | 177 |
Who archives the data?
