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

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.

• Type: Case Set
• Archiver: The database of Genotypes and Phenotypes (dbGaP)