Package: CNVRanger
Version: 1.3.3
Title: Summarization and expression/phenotype association of CNV ranges
Author: Ludwig Geistlinger [aut, cre], Vinicius Henrique da Silva [aut],
    Marcel Ramos [ctb], Levi Waldron [ctb]
Maintainer: Ludwig Geistlinger <ludwig.geistlinger@sph.cuny.edu>
Depends: GenomicRanges, RaggedExperiment
Imports: 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, curatedTCGAData, ensembldb, grid, knitr, regioneR,
        rmarkdown
Description: 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.
License: Artistic-2.0
BugReports: https://github.com/waldronlab/CNVRanger/issues
Encoding: UTF-8
VignetteBuilder: knitr
biocViews: CopyNumberVariation, DifferentialExpression, GeneExpression,
        GenomeWideAssociation, GenomicVariation, Microarray, RNASeq,
        SNP
RoxygenNote: 7.0.0
git_url: https://git.bioconductor.org/packages/CNVRanger
git_branch: master
git_last_commit: 93b1be4
git_last_commit_date: 2019-12-03
Date/Publication: 2019-12-03
NeedsCompilation: no
Packaged: 2019-12-04 04:45:51 UTC; biocbuild
Built: R 4.0.0; ; 2019-12-04 13:08:26 UTC; unix
