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
Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing
Illumina HiSeq 2000 1

Who archives the data?

There are no publications available