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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

MaintainerRuining Dong <lnyidrn@gmail.com>
AuthorRuining Dong [aut, cre] (ORCID: <https://orcid.org/0000-0003-1433-0484>)
LicenseGPL-3 + file LICENSE
Bug Reportshttps://github.com/PapenfussLab/svaNUMT/issues
Downloads rank261
Source branchRELEASE_3_23
biocViewsAnnotation, 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