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URL: http://www.bioconductor.org/packages/devel/bioc/html/CNVrd2.html
Proper Citation: CNVrd2 (RRID:SCR_001723)
Description: A software package that uses next-generation sequencing data to measure human gene copy number for multiple samples, indentify SNPs tagging copy number variants and detect copy number polymorphic genomic regions.
Synonyms: CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data
Resource Type: software resource
Defining Citation: PMID:23646200
Keywords: standalone software, illumina, unix/linux, mac os x, windows, r, clustering., copy number variation, coverage, linkage disequilibrium, snp, sequencing
Availability: Free, Available for download, Freely available
Resource Name: CNVrd2
Resource ID: SCR_001723
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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
