Agilent whole exome hybridisation capture will be performed on genomic DNA derived from 25 renal cancers and matched normal DNA from the same patients. Three lanes of Illumina GA sequencing will be performed on the resulting 50 exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes.
- Type: Cancer Genomics
- Archiver: EGA European Genome-Phenome Archive
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
|EGAD00000000051||Illumina Genome Analyzer II||25|
|EGAD00001000001||Illumina Genome Analyzer II||18|
|EGAD00001000014||Illumina Genome Analyzer II||54|
|EGAD00001000287||Illumina Genome Analyzer II||54|
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.
Nature 469: 2011 539-542