The Genomic Complexity of Primary Human Prostate Cancer
Seven primary prostate cancers and their paired normal counterparts were DNA-sequenced on a massively parallel sequencing platform. This approach was taken to investigate the genomes for mutations and genomic alterations that would be undetectable by lower-resolution methods. As result, tumors containing chains of balanced rearrangements that occurred within or adjacent to known cancer genes were discovered.
- Type: Cohort
- Archiver: The database of Genotypes and Phenotypes (dbGaP)