URL: http://compbio.cs.utoronto.ca/varid/
Proper Citation: VARiD (RRID:SCR_000241)
Description: Software using a Hidden Markov Model for SNP (single nucleotide polymorphism) and indel identification with AB-SOLiD color-space as well as regular letter-space reads.
Abbreviations: VARiD
Resource Type: software resource
Defining Citation: PMID:20529926
Keywords: c, single nucleotide polymorphism, indel, bio.tools
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