Package: geneAttribution
Type: Package
Title: Identification of candidate genes associated with genetic
        variation
Version: 1.38.0
Date: 2025-07-24
Author: Arthur Wuster
Maintainer: Arthur Wuster <wustera@gene.com>
Description: Identification of the most likely gene or genes through
        which variation at a given genomic locus in the human genome
        acts. The most basic functionality assumes that the closer gene
        is to the input locus, the more likely the gene is to be
        causative. Additionally, any empirical data that links genomic
        regions to genes (e.g. eQTL or genome conformation data) can be
        used if it is supplied in the UCSC .BED file format.
License: Artistic-2.0
biocViews: SNP, GenePrediction, GenomeWideAssociation,
        VariantAnnotation, GenomicVariation
Imports: utils, GenomicRanges, org.Hs.eg.db, BiocGenerics, Seqinfo,
        GenomicFeatures, IRanges, rtracklayer
Suggests: TxDb.Hsapiens.UCSC.hg38.knownGene,
        TxDb.Hsapiens.UCSC.hg19.knownGene, knitr, rmarkdown, testthat
RoxygenNote: 5.0.1
VignetteBuilder: knitr
Config/pak/sysreqs: make libbz2-dev liblzma-dev libpng-dev libxml2-dev
        libssl-dev xz-utils zlib1g-dev
Repository: Bioconductor 3.23
Date/Publication: 2026-04-28 12:44:06 UTC
RemoteUrl: https://github.com/bioc/geneAttribution
RemoteRef: RELEASE_3_23
RemoteSha: 73393b236e25d5a9b05a298c5c5a3737da30d0a1
NeedsCompilation: no
Packaged: 2026-10-03 07:27:23 UTC; root