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varitas: Variant Calling in Targeted Analysis Sequencing Data

Multi-caller variant analysis pipeline for targeted analysis sequencing (TAS) data. Features a modular, automated workflow that can start with raw reads and produces a user-friendly PDF summary and a spreadsheet containing consensus variant information.

Version:0.0.2
Imports:stringr,dplyr,yaml,openxlsx,VennDiagram,assertthat,magrittr, tools, utils,tidyr,doParallel,foreach
Suggests:testthat,knitr,rmarkdown,futile.logger
Published:2020-11-14
DOI:10.32614/CRAN.package.varitas
Author:Adam Mills [aut, cre], Erle Holgersen [aut], Ros Cutts [aut], Syed Haider [aut]
Maintainer:Adam Mills <Adam.Mills at icr.ac.uk>
License:GPL-2
NeedsCompilation:no
SystemRequirements:perl, bedtools (>=2.27.1), bwa
Materials:NEWS
CRAN checks:varitas results

Documentation:

Reference manual:varitas.html ,varitas.pdf
Vignettes:Errors (source,R code)
Introduction (source,R code)

Downloads:

Package source: varitas_0.0.2.tar.gz
Windows binaries: r-devel:varitas_0.0.2.zip, r-release:varitas_0.0.2.zip, r-oldrel:varitas_0.0.2.zip
macOS binaries: r-release (arm64):varitas_0.0.2.tgz, r-oldrel (arm64):varitas_0.0.2.tgz, r-release (x86_64):varitas_0.0.2.tgz, r-oldrel (x86_64):varitas_0.0.2.tgz
Old sources: varitas archive

Linking:

Please use the canonical formhttps://CRAN.R-project.org/package=varitasto link to this page.


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