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URL: http://cran.r-project.org/web/packages/ExomeDepth/
Proper Citation: ExomeDepth (RRID:SCR_002663)
Description: Software that calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
Resource Type: software resource
Defining Citation: PMID:22942019
Keywords: software package, unix/linux, mac os x, windows, r, bio.tools
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