fluentGenomics
A plyranges and tximeta workflow
Bioconductor version: 3.23 · Package version: 1.24.0
An extended workflow using the plyranges and tximeta packages for fluent genomic data analysis. Use tximeta to correctly import RNA-seq transcript quantifications and summarize them to gene counts for downstream analysis. Use plyranges for clearly expressing operations over genomic coordinates and to combine results from differential expression and differential accessibility analyses.
Installation
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("fluentGenomics") Details
| Maintainer | Stuart Lee <stuart.andrew.lee@gmail.com> |
| Author | Stuart Lee [aut, cre] (ORCID: <https://orcid.org/0000-0003-1179-8436>), Michael Love [aut, ctb] |
| License | MIT + file LICENSE |
| URL | https://github.com/sa-lee/fluentGenomics |
| Bug Reports | https://github.com/sa-lee/fluentGenomics/issues |
| Downloads rank | 74 |
| Source branch | RELEASE_3_23 |
| biocViews | BasicWorkflow, GeneExpressionWorkflow, Workflow |
Download
Dependencies
Depends: R (>= 4.0)
Imports: plyranges (>= 1.7.7), dplyr, SummarizedExperiment, readr, stats, utils
Suggests: knitr, rmarkdown, bookdown, rappdirs, BiocFileCache, DESeq2, limma, ggplot2, tidyr, tximeta (>= 1.4.2), macrophage (>= 1.2.0)