PV Exome Study

Study ID Alternative Stable ID Type
EGAS00001000028 Cancer Genomics

Study Description

Agilent whole exome hybridisation capture will be performed on genomic DNA derived from 50 Polycythemia Vera Myeloproliferative Disease samples and matched normal DNA from the same patients. Three lanes of Illumina GA sequencing will be performed on the resulting 100 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
Polycythemia Vera Myeloproliferative Disease exome sequencing
Illumina Genome Analyzer II,Illumina HiSeq 2000 119

Who archives the data?

There are no publications available