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?

There are no publications available