Package: Rariant
Type: Package
Title: Identification and Assessment of Single Nucleotide Variants
        through Shifts in Non-Consensus Base Call Frequencies
Version: 1.20.0
Author: Julian Gehring, Simon Anders, Bernd Klaus
Maintainer: Julian Gehring <jg-bioc@gmx.com>
Imports: methods, BiocGenerics, S4Vectors, IRanges, GenomeInfoDb,
        ggbio, ggplot2, exomeCopy, SomaticSignatures, Rsamtools, shiny,
        VGAM, dplyr, reshape2
Depends: R (>= 3.0.2), GenomicRanges, VariantAnnotation
Suggests: h5vcData, testthat, knitr, optparse,
        BSgenome.Hsapiens.UCSC.hg19
Description: The 'Rariant' package identifies single nucleotide variants from sequencing data based on the difference of binomially distributed mismatch rates between matched samples.
VignetteBuilder: knitr
Encoding: UTF-8
ByteCompile: TRUE
License: GPL-3
URL: https://github.com/juliangehring/Rariant
BugReports: https://support.bioconductor.org
LazyLoad: yes
biocViews: Sequencing, StatisticalMethod, GenomicVariation,
        SomaticMutation, VariantDetection, Visualization
git_url: https://git.bioconductor.org/packages/Rariant
git_branch: RELEASE_3_9
git_last_commit: 3b91ad3
git_last_commit_date: 2019-05-02
Date/Publication: 2019-05-02
NeedsCompilation: no
Packaged: 2019-05-03 03:15:22 UTC; biocbuild
Built: R 3.6.0; ; 2019-05-03 14:13:58 UTC; windows
