DOI: 10.18129/B9.bioc.CrispRVariants    

This is the development version of CrispRVariants; for the stable release version, see CrispRVariants.

Tools for counting and visualising mutations in a target location

Bioconductor version: Development (3.7)

CrispRVariants provides tools for analysing the results of a CRISPR-Cas9 mutagenesis sequencing experiment, or other sequencing experiments where variants within a given region are of interest. These tools allow users to localize variant allele combinations with respect to any genomic location (e.g. the Cas9 cut site), plot allele combinations and calculate mutation rates with flexible filtering of unrelated variants.

Author: Helen Lindsay [aut, cre]

Maintainer: Helen Lindsay <helen.lindsay at>

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biocViews CRISPR, DataRepresentation, GeneticVariability, GenomicVariation, Software, VariantDetection, Visualization
Version 1.7.4
In Bioconductor since BioC 3.3 (R-3.3) (2 years)
License GPL-2
Depends R (>= 3.4), ggplot2 (>= 2.2.0)
Imports AnnotationDbi, BiocParallel, Biostrings, methods, GenomeInfoDb, GenomicAlignments, GenomicRanges, grDevices, grid, gridExtra, IRanges, reshape2, Rsamtools, S4Vectors(>= 0.9.38), utils
Suggests BiocStyle, gdata, GenomicFeatures, knitr, rmarkdown, rtracklayer, sangerseqR, testthat, VariantAnnotation
Depends On Me
Imports Me
Suggests Me
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