Study
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 |
|---|---|---|---|
| EGAD00001000098 |
FRCC Exome sequencing
|
Illumina Genome Analyzer II | 16 |
Who archives the data?
