Cancer Genome Libraries Tests

Study ID Alternative Stable ID Type
EGAS00001000208 Whole Genome Sequencing

Study Description

Testing library production.Genomic libraries (500 bps) will be generated from total genomic DNA derived from commomon epithelial cancer samples and subjected to paired end sequencing on the llumina plateforms. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.

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
Cancer Genome Libraries Tests
Illumina Genome Analyzer II 16

Who archives the data?

There are no publications available