パッケージ: minimap2 (2.24+dfsg-3 など)
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.
その他の minimap2 関連パッケージ
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- dep: libc6 (>= 2.34)
- GNU C ライブラリ: 共有ライブラリ
以下のパッケージによって提供される仮想パッケージでもあります: libc6-udeb
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- dep: zlib1g (>= 1:1.1.4)
- 圧縮ライブラリ - ランタイム
minimap2 のダウンロード
アーキテクチャ | バージョン | パッケージサイズ | インストールサイズ | ファイル |
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amd64 | 2.24+dfsg-3+b1 | 377.2 kB | 498.0 kB | [ファイル一覧] |
arm64 | 2.24+dfsg-3+b1 | 369.0 kB | 510.0 kB | [ファイル一覧] |
armel | 2.24+dfsg-3+b1 | 386.7 kB | 545.0 kB | [ファイル一覧] |
armhf | 2.24+dfsg-3+b1 | 388.1 kB | 477.0 kB | [ファイル一覧] |
i386 | 2.24+dfsg-3+b1 | 384.2 kB | 525.0 kB | [ファイル一覧] |
mips64el | 2.24+dfsg-3+b1 | 402.3 kB | 582.0 kB | [ファイル一覧] |
mipsel | 2.24+dfsg-3+b1 | 412.6 kB | 645.0 kB | [ファイル一覧] |
ppc64el | 2.24+dfsg-3+b1 | 389.0 kB | 574.0 kB | [ファイル一覧] |
s390x | 2.24+dfsg-3+b1 | 389.4 kB | 567.0 kB | [ファイル一覧] |