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
| Maintainer | Stevie Pederson <stephen.pederson.au@gmail.com> |
| Author | Stevie Pederson [aut, cre] (ORCID: <https://orcid.org/0000-0001-8197-3303>) |
| License | GPL-3 |
| URL | https://github.com/smped/transmogR |
| Bug Reports | https://github.com/smped/transmogR/issues |
| Downloads rank | 185 |
| Source branch | RELEASE_3_23 |
| biocViews | Alignment, GenomicVariation, Sequencing, Software, TranscriptomeVariant, VariantAnnotation |
Documentation
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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)