wip/subread 2.1.0 NetBSD

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.