Study
Familial Thrombocytosis germline exome sequencing
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000088 | Cancer Genomics |
Study Description
Agilent whole exome hybridisation capture will be performed on genomic DNA derived from 3 relatives from a family with multiple affected familial thrombocytosis (FT) patients. Germline DNA from 2-4 patients affected with FT will be used to prepare libraries and sequenced in one lane of HiSeq sequencing, 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 |
|---|---|---|---|
| EGAD00001000128 |
Familial Thrombocytosis germline exome sequencing
|
Illumina HiSeq 2000 | 4 |
Who archives the data?
