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

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 <[email protected]>
URL https://github.com/juliangehring/Rariant
Package repositoryView on Bioconductor
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Rariant documentation built on May 6, 2019, 3:05 a.m.