URL: https://gatk.broadinstitute.org/hc/en-us/articles/360037593851-Mutect2
Proper Citation: Mutect2 (RRID:SCR_026692)
Description: Software tool to call somatic short mutations via local assembly of haplotypes. Somatic variant caller that uses local assembly and realignment to detect SNVs and indels.
Resource Type: software application, software resource
Defining Citation: DOI:10.1101/861054
Keywords: Somatic variant caller, call somatic short mutations, detect SNVs and indels,
Resource Name: Mutect2
Resource ID: SCR_026692
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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
