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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
Availability: Free, Available for download, Freely available
Resource Name: ExomeDepth
Resource ID: SCR_002663
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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
The data sets included in this resource are published in Kravitz et al, 2012. Distinct roles for direct and indirect pathway striatal neurons in reinforcement (Nat. Neurosci).
