ExomeDepth: Calls Copy Number Variants from Targeted Sequence Data

Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders. The method is presented in details in Plagnol et al (2012) <https://pubmed.ncbi.nlm.nih.gov/22942019/>.

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Package details

AuthorVincent Plagnol [aut, cre], Gerard Jungman [ctb] (Author of included GSL fragments), Brian Gough [ctb] (Author of included GSL fragments), Jorma O Tahtinen [ctb] (Author of included GSL fragments), Gert Van den Eynde [ctb] (Author of included GSL fragments)
MaintainerVincent Plagnol <vincent.plagnol@gmail.com>
Package repositoryView on CRAN
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ExomeDepth documentation built on Nov. 3, 2022, 5:05 p.m.