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transmogR

Modify a set of reference sequences using a set of variants

Bioconductor version: 3.23 · Package version: 1.8.1

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.

Installation

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

BiocManager::install("transmogR")

Details

MaintainerStevie Pederson <stephen.pederson.au@gmail.com>
AuthorStevie Pederson [aut, cre] (ORCID: <https://orcid.org/0000-0001-8197-3303>)
LicenseGPL-3
URLhttps://github.com/smped/transmogR
Bug Reportshttps://github.com/smped/transmogR/issues
Downloads rank185
Source branchRELEASE_3_23
biocViewsAlignment, GenomicVariation, Sequencing, Software, TranscriptomeVariant, VariantAnnotation

Documentation

Download

Dependencies

Depends: R (>= 4.1.0), Biostrings, GenomicRanges

Imports: BSgenome, data.table, Seqinfo, GenomicFeatures, ggplot2 (>= 4.0.0), IRanges, jsonlite, matrixStats, methods, parallel, patchwork, scales, stats, S4Vectors, SummarizedExperiment, VariantAnnotation

Suggests: BiocStyle, BSgenome.Hsapiens.UCSC.hg38, edgeR, extraChIPs, InteractionSet, knitr, readr, rmarkdown, rtracklayer, SimpleUpset, testthat (>= 3.0.0)