VarScan published
June 23rd, 2009
VarScan, a tool developed at The Genome Center to detect variants in massively parallel sequence data has been published in Bioinformatics. 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.
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Tagged with: 454, genomics, Illumina, informatics, science, software, wustl
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