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transmogR
This is the released version of transmogR; for the devel version, see transmogR.
Modify a set of reference sequences using a set of variants
Bioconductor version: Release (3.22)
transmogR provides the tools needed to crate a new reference genome or reference transcriptome, using a set of variants. Variants can be any combination of SNPs, Insertions and Deletions. The intended use-case is to enable creation of variant-modified reference transcriptomes for incorporation into transcriptomic pseudo-alignment workflows, such as salmon.
Author: Stevie Pederson [aut, cre] ORCID iD ORCID: 0000-0001-8197-3303
Maintainer: Stevie Pederson <stephen.pederson.au at gmail.com>
citation("transmogR")):
Installation
To install this package, start R (version "4.5") and enter:
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("transmogR")
For older versions of R, please refer to the appropriate Bioconductor release.
Documentation
To view documentation for the version of this package installed in your system, start R and enter:
browseVignettes("transmogR")
Details
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Package Archives
Follow Installation instructions to use this package in your R session.