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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
Availability: Free, Available for download, Freely available
Resource Name: VARiD
Resource ID: SCR_000241
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
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