Study
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 |
|---|---|---|---|
| EGAD00001000094 |
Cancer Genome Libraries Tests
|
Illumina Genome Analyzer II | 16 |
Who archives the data?
