Artifact minimap2_2.24+dfsg-3+b1_arm64

Metadata
deb_control_files:
- control
- md5sums
deb_fields:
  Architecture: arm64
  Depends: libc6 (>= 2.34), zlib1g (>= 1:1.1.4)
  Description: |-
    versatile pairwise aligner for genomic and spliced nucleotide sequences
     Minimap2 is a versatile sequence alignment program that aligns DNA or
     mRNA sequences against a large reference database. Typical use cases
     include: (1) mapping PacBio or Oxford Nanopore genomic reads to the
     human genome; (2) finding overlaps between long reads with error rate up
     to ~15%; (3) splice-aware alignment of PacBio Iso-Seq or Nanopore cDNA
     or Direct RNA reads against a reference genome; (4) aligning Illumina
     single- or paired-end reads; (5) assembly-to-assembly alignment; (6) full-
     genome alignment between two closely related species with divergence
     below ~15%.
     .
     For ~10kb noisy reads sequences, minimap2 is tens of times faster than
     mainstream long-read mappers such as BLASR, BWA-MEM, NGMLR and GMAP. It
     is more accurate on simulated long reads and produces biologically
     meaningful alignment ready for downstream analyses. For >100bp Illumina
     short reads, minimap2 is three times as fast as BWA-MEM and Bowtie2, and
     as accurate on simulated data. Detailed evaluations are available from
     the minimap2 paper or the preprint.
  Homepage: https://github.com/lh3/minimap2
  Installed-Size: '510'
  Maintainer: Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org>
  Package: minimap2
  Priority: optional
  Section: science
  Source: minimap2 (2.24+dfsg-3)
  Version: 2.24+dfsg-3+b1
srcpkg_name: minimap2
srcpkg_version: 2.24+dfsg-3

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