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[ Source: minimap2  ]

Package: minimap2 (2.24+dfsg-3 and others)

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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.

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Download minimap2

Download for all available architectures
Architecture Version Package Size Installed Size Files
amd64 2.24+dfsg-3+b1 377.2 kB498.0 kB [list of files]
arm64 2.24+dfsg-3+b1 369.0 kB510.0 kB [list of files]
armel 2.24+dfsg-3+b1 386.7 kB545.0 kB [list of files]
armhf 2.24+dfsg-3+b1 388.1 kB477.0 kB [list of files]
i386 2.24+dfsg-3+b1 384.2 kB525.0 kB [list of files]
mips64el 2.24+dfsg-3+b1 402.3 kB582.0 kB [list of files]
mipsel 2.24+dfsg-3+b1 412.6 kB645.0 kB [list of files]
ppc64el 2.24+dfsg-3+b1 389.0 kB574.0 kB [list of files]
s390x 2.24+dfsg-3+b1 389.4 kB567.0 kB [list of files]