Rariant: Identification and Assessment of Single Nucleotide Variants through Shifts in Non-Consensus Base Call Frequencies
Version 1.12.0

The 'Rariant' package identifies single nucleotide variants from sequencing data based on the difference of binomially distributed mismatch rates between matched samples.

Package details

AuthorJulian Gehring, Simon Anders, Bernd Klaus
Bioconductor views GenomicVariation Sequencing SomaticMutation StatisticalMethod VariantDetection Visualization
MaintainerJulian Gehring <jg-bioc@gmx.com>
LicenseGPL-3
Version1.12.0
URL https://github.com/juliangehring/Rariant
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R:
source("https://bioconductor.org/biocLite.R")
biocLite("Rariant")

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Rariant documentation built on May 31, 2017, 11 a.m.