URL: https://github.com/etal/cnvkit
Proper Citation: CNVkit (RRID:SCR_021917)
Description: Software command line toolkit and Python library for detecting copy number variants and alterations genome wide from hight hroughput sequencing.
Resource Type: software resource, software toolkit
Keywords: detecting copy number variants, alterations genome wide, hight hroughput sequencing
Availability: Free, Available for download, Freely available
Resource Name: CNVkit
Resource ID: SCR_021917
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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
