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CNVRanger

Summarization and expression/phenotype association of CNV ranges

Bioconductor version: 3.24 · Package version: 1.29.4

Other Bioconductor versions

devel is the development version; release is the current stable one.

3.24 (devel), 3.23 (release)

The CNVRanger package implements a comprehensive tool suite for CNV analysis. This includes functionality for summarizing individual CNV calls across a population, assessing overlap with functional genomic regions, and association analysis with gene expression and quantitative phenotypes.

DOI: 10.18129/B9.bioc.CNVRanger

Installation

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

BiocManager::install("CNVRanger")

Details

MaintainerLudwig Geistlinger <ludwig.geistlinger@gmail.com>
AuthorLudwig Geistlinger [aut, cre] (ORCID: <https://orcid.org/0000-0002-2495-5464>), Vinicius Henrique da Silva [aut], Marcel Ramos [ctb] (ORCID: <https://orcid.org/0000-0002-3242-0582>), Levi Waldron [ctb] (ORCID: <https://orcid.org/0000-0003-2725-0694>)
LicenseArtistic-2.0
Bug Reportshttps://github.com/waldronlab/CNVRanger/issues
Source branchdevel
Build report Bioconductor build system, r-universe
biocViewsCopyNumberVariation, DifferentialExpression, GeneExpression, GenomeWideAssociation, GenomicVariation, Microarray, RNASeq, SNP, Software
Package Short Url https://bioconductor.org/packages/CNVRanger/

Citation

From within R, enter citation("CNVRanger"):

Ludwig Geistlinger, Vinicius Henrique da Silva. CNVRanger: Summarization and expression/phenotype association of CNV ranges. doi:10.18129/B9.bioc.CNVRanger, R package version 1.29.4, https://bioconductor.org/packages/CNVRanger.

Generated from the package metadata; it may differ from the package's own citation.

Documentation

Download

Follow the installation instructions to use this package in your R session.

Source packageCNVRanger_1.29.4.tar.gz
Windows binary (x86_64)CNVRanger_1.29.4.zip
macOS binary (arm64)CNVRanger_1.29.4.tgz
macOS binary (x86_64)CNVRanger_1.29.4.tgz
Dependencies

Depends: GenomicRanges, RaggedExperiment

Imports: BiocGenerics, BiocParallel, GDSArray, GenomeInfoDb, IRanges, S4Vectors, SNPRelate, SummarizedExperiment, data.table, edgeR, gdsfmt, grDevices, lattice, limma, methods, plyr, qqman, rappdirs, reshape2, stats, utils

Suggests: AnnotationHub, BSgenome.Btaurus.UCSC.bosTau6.masked, BiocStyle, ComplexHeatmap, Gviz, MultiAssayExperiment, TCGAutils, TxDb.Hsapiens.UCSC.hg19.knownGene, curatedTCGAData, ensembldb, grid, knitr, org.Hs.eg.db, regioneR, rmarkdown, statmod