Renal_Cancer_Exome_Sequencing - EGA European Genome-Phenome Archive

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.

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	Sequencing data from matching Renal Carcinoma samples 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 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. 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. 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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