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?

There are no publications available