Study
Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000139 | Cancer Genomics |
Study Description
Agilent whole exome hybridisation capture will be performed on genomic DNA derived from ~3 Splenic Marginal Zone Lymphoma with villous lymphocytes samples and matched normal DNA from the same patients. Samples will be multiplexed in one lane of Illumina HiSeq. Sequencing to a coverage of at least 30x will be performed 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 |
|---|---|---|---|
| EGAD00001000081 |
Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing
|
Illumina HiSeq 2000 | 1 |
Who archives the data?
