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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
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.pdf
Vignettes: Errors
Introduction

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 form https://CRAN.R-project.org/package=varitas to link to this page.

These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
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