Study
Sequencing of Cervical Cancer
Study ID | Alternative Stable ID | Type |
---|---|---|
phs000723 | Case-Control |
Study Description
Precision mapping of genetic alterations in cancer can enable better selection of therapies and improved outcomes when combined with new sequencing diagnostics. We describe whole-exome sequences from cervical adenocarcinomas and paired normal samples in Hong Kong Chinese women. These data uncover a heterogeneous genomic landscape but identify commonly aberrant loci including FAT1, ARID1A, ERBB2 and PIK3CA that may provide a focus for the development of individualized targeted therapies for Chinese women with cervical adenocarcinoma.
Archive | Link Archive Accession |
---|---|
dbGaP | phs000723 |
Who archives the data?
