biology/subread - The NetBSD Packages Collection

High-performance read alignment, quantification and mutation discovery

The Subread package comprises a suite of software programs for
processing next-gen sequencing read data including:

    Subread: a general-purpose read aligner which can align both
    genomic DNA-seq and RNA-seq reads. It can also be used to
    discover genomic mutations including short indels and structural
    variants.

    Subjunc: a read aligner developed for aligning RNA-seq reads
    and for the detection of exon-exon junctions. Gene fusion events
    can be detected as well.

    featureCounts: a software program developed for counting
    reads to genomic features such as genes, exons, promoters and
    genomic bins.

    Sublong: a long-read aligner that is designed based on
    seed-and-vote.

    exactSNP: a SNP caller that discovers SNPs by testing signals
    against local background noises.

Build dependencies

pkgtools/mktools devel/gmake pkgtools/cwrappers

Runtime dependencies

(none)

Binary packages

OSArchitectureVersion
(none)

Binary packages can be installed with the high-level tool pkgin (which can be installed with pkg_add) or pkg_add(1) (installed by default). The NetBSD packages collection is also designed to permit easy installation from source.

Available build options

(none)

Known vulnerabilities

The pkg_admin audit command locates any installed package which has been mentioned in security advisories as having vulnerabilities.

Please note the vulnerabilities database might not be fully accurate, and not every bug is exploitable with every configuration.


Problem reports, updates or suggestions for this package should be reported with send-pr.