svaNUMT
NUMT detection from structural variant calls
Bioconductor version: 3.23 · Package version: 1.18.0
svaNUMT contains functions for detecting NUMT events from structural variant calls. It takes structural variant calls in GRanges of breakend notation and identifies NUMTs by nuclear-mitochondrial breakend junctions. The main function reports candidate NUMTs if there is a pair of valid insertion sites found on the nuclear genome within a certain distance threshold. The candidate NUMTs are reported by events.
Installation
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("svaNUMT") Details
| Maintainer | Ruining Dong <lnyidrn@gmail.com> |
| Author | Ruining Dong [aut, cre] (ORCID: <https://orcid.org/0000-0003-1433-0484>) |
| License | GPL-3 + file LICENSE |
| Bug Reports | https://github.com/PapenfussLab/svaNUMT/issues |
| Downloads rank | 261 |
| Source branch | RELEASE_3_23 |
| biocViews | Annotation, DataImport, Genetics, Sequencing, Software, VariantAnnotation |
Documentation
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Dependencies
Depends: GenomicRanges, rtracklayer, VariantAnnotation, StructuralVariantAnnotation, BiocGenerics, Biostrings, R (>= 4.0)
Imports: assertthat, stringr, dplyr, methods, rlang, S4Vectors, Seqinfo, GenomeInfoDb, GenomicFeatures, pwalign
Suggests: TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome.Hsapiens.UCSC.hg19, ggplot2, devtools, testthat (>= 2.1.0), roxygen2, knitr, readr, plyranges, circlize, IRanges, SummarizedExperiment, rmarkdown