Log message:
biology/subread: Alignment, quantification, SNPs

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.