Study

Exome Sequencing of Clear Cell Endometrial Tumors and Paired Non-tumor Samples

Study ID Alternative Stable ID Type
phs000967 Case Set

Study Description

The purpose of this study was to identify somatic (tumor-specific) mutations in clear cell endometrial tumor exomes. The dataset was generated at the NIH Intramural Sequencing Center (NISC) and NHGRI by next generation sequencing the exomes of 16 de-identified primary tumor DNAs and matched non-tumor DNAs.

Archive Link Archive Accession
dbGaP phs000967

Who archives the data?

There are no publications available