Study

Renal_Matched_Pair_Cell_Line_Exome_Sequencing

Study ID Alternative Stable ID Type
EGAS00001000179 Cancer Genomics

Study Description

Agilent whole exome hybridisation capture will be performed on genomic DNA derived from renal cancer cell lines and matched normal DNA from the same patient. Illumina GA sequencing will be performed on the resulting exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes.

Study Datasets 1 dataset.

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
EGAD00001000100
Renal Matched Pair Cell Line Exome Sequencing
Illumina Genome Analyzer II 10

Who archives the data?

There are no publications available