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URL: http://snver.sourceforge.net/
Proper Citation: SNVer (RRID:SCR_002061)
Description: Statistical software tool for calling common and rare variants in analysis of pool or individual next-generation sequencing data. This software is optimized for analysis of whole-exome sequencing data and whole-genome sequencing data.
Resource Type: data analysis software, data processing software, software application, software resource
Defining Citation: PMID:21813454
Keywords: statistical analysis software, sequencing, dna, whole-exome, whole-genome, variant, bio.tools
Availability: Free, Available for download, Freely available
Resource Name: SNVer
Resource ID: SCR_002061
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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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