Study

Renal_Cancer_Exome_Sequencing

Study ID Alternative Stable ID Type
EGAS00001000006 Cancer Genomics

Study Description

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.

Study Datasets 4 datasets.

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Dataset ID Description Technology Samples
EGAD00000000051
Sequencing data from matching Renal Carcinoma samples
Illumina Genome Analyzer II 25
EGAD00001000001
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
Illumina Genome Analyzer II 18
EGAD00001000014
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.
Illumina Genome Analyzer II 54
EGAD00001000287
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.
Illumina Genome Analyzer II 54

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