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ExomeDepth  

Calls Copy Number Variants from Targeted Sequence Data
View on CRAN: Click here


Download and install ExomeDepth package within the R console
Install from CRAN:
install.packages("ExomeDepth")

Install from Github:
library("remotes")
install_github("cran/ExomeDepth")

Install by package version:
library("remotes")
install_version("ExomeDepth", "1.1.16")



Attach the package and use:
library("ExomeDepth")
Maintained by
Vincent Plagnol
[Scholar Profile | Author Map]
All associated links for this package
First Published: 2022-11-03
Latest Update:
Description:
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) .
How to cite:
Vincent Plagnol (2022). ExomeDepth: Calls Copy Number Variants from Targeted Sequence Data. R package version 1.1.16, https://cran.r-project.org/web/packages/ExomeDepth. Accessed 21 Sep. 2026.
Previous versions and publish date:
1.1.16 (2022-11-03 17:00), (2026-07-09 08:03)
Other packages that cited ExomeDepth R package
View ExomeDepth citation profile
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