MMAPPR2 maps mutations resulting from pooled RNA-seq data from the F2 cross of forward genetic screens. Its predecessor is described in a paper published in Genome Research (Hill et al. 2013). MMAPPR2 accepts aligned BAM files as well as a reference genome as input, identifies loci of high sequence disparity between the control and mutant RNA sequences, predicts variant effects using Ensembl's Variant Effect Predictor, and outputs a ranked list of candidate mutations.
Package details |
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Bioconductor views | DNASeq PooledScreens RNASeq VariantDetection |
Maintainer | |
License | GPL-3 |
Version | 0.99.22 |
URL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613585/ https://github.com/kjohnsen/MMAPPR2 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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