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URL: http://mrcanavar.sourceforge.net/
Proper Citation: mrCaNaVaR (RRID:SCR_003135)
Description: Copy number caller that analyzes the whole-genome next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.
Abbreviations: mrCaNaVaR
Synonyms: mrCaNaVaR - micro-read Copy Number Variant Regions, micro-read Copy Number Variant Regions
Resource Type: software resource
Keywords: genome, next-generation sequence, duplication, deletion, copy number variant, bio.tools
Availability: Free, Freely available
Resource Name: mrCaNaVaR
Resource ID: SCR_003135
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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
