VarScan published
June 23rd, 2009
, a tool developed at to detect variants in massively parallel sequence data has been published in . VarScan can process both 454 and Solexa data of individuals or pools. You can find more information about VarScan in a post by Dan Koboldt, one of the paper’s and VarScan’s authors.
Posted in genomics | No Comments »
Tagged with: 454, genomics, Illumina, informatics, science, software, wustl
You can follow any responses to this entry through the feed. You can leave a response, or trackback from your own site.
Leave a Reply