The 'Rariant' package identifies single nucleotide variants from sequencing data based on the difference of binomially distributed mismatch rates between matched samples.
|Author||Julian Gehring, Simon Anders, Bernd Klaus (EMBL Heidelberg)|
|Bioconductor views||GenomicVariation Sequencing SomaticMutation StatisticalMethod VariantDetection Visualization|
|Maintainer||Julian Gehring <firstname.lastname@example.org>|
|Package repository||View on GitHub|
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