Familial_Thrombocytosis_germline_exome_sequencing

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.

Type: Cancer Genomics
Archiver: EGA European Genome-Phenome Archive

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