FRCC Exome sequencing

Study ID Alternative Stable ID Type
EGAS00001000176 Cancer Genomics

Study Description

Agilent whole exome hybridisation capture will be performed on genomic DNA derived from FRCC patients. one lane of Illumina Hiseq 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
FRCC Exome sequencing
Illumina Genome Analyzer II 16

Who archives the data?

There are no publications available