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Rmmquant

RNA-Seq multi-mapping Reads Quantification Tool

Bioconductor version: 3.23 · Package version: 1.30.0

RNA-Seq is currently used routinely, and it provides accurate information on gene transcription. However, the method cannot accurately estimate duplicated genes expression. Several strategies have been previously used, but all of them provide biased results. With Rmmquant, if a read maps at different positions, the tool detects that the corresponding genes are duplicated; it merges the genes and creates a merged gene. The counts of ambiguous reads is then based on the input genes and the merged genes. Rmmquant is a drop-in replacement of the widely used tools findOverlaps and featureCounts that handles multi-mapping reads in an unabiased way.

Installation

if (!require("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("Rmmquant")

Details

MaintainerZytnicki Matthias <matthias.zytnicki@inra.fr>
AuthorZytnicki Matthias [aut, cre]
LicenseGPL-3
System RequirementsC++11
Downloads rank441
Source branchRELEASE_3_23
biocViewsGeneExpression, Software, Transcription

Documentation

Download

Follow the installation instructions to use this package in your R session.

Source packageRmmquant_1.30.0.tar.gz
Windows binary (x86_64)Rmmquant_1.30.0.zip
macOS binary (arm64)Rmmquant_1.30.0.tgz
macOS binary (x86_64)Rmmquant_1.30.0.tgz
Dependencies

Depends: R (>= 3.6)

Imports: Rcpp (>= 0.12.8), methods, S4Vectors, GenomicRanges, SummarizedExperiment, devtools, TBX20BamSubset, TxDb.Mmusculus.UCSC.mm9.knownGene, org.Mm.eg.db, DESeq2, apeglm, BiocStyle

LinkingTo: Rcpp

Suggests: knitr, rmarkdown, testthat