An integrative variant analysis suite for whole exome next-generation sequencing data
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Open Access
- 12 January 2012
- journal article
- Published by Springer Nature in BMC Bioinformatics
- Vol. 13 (1), 8
- https://doi.org/10.1186/1471-2105-13-8
Abstract
Whole exome capture sequencing allows researchers to cost-effectively sequence the coding regions of the genome. Although the exome capture sequencing methods have become routine and well established, there is currently a lack of tools specialized for variant calling in this type of data.Keywords
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