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?
