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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.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00000000051 Illumina Genome Analyzer II 25
EGAD00001000001 Illumina Genome Analyzer II 18
EGAD00001000014 Illumina Genome Analyzer II 54
EGAD00001000287 Illumina Genome Analyzer II 54
Publications Citations
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.
Nature 469: 2011 539-542