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[ Source: vt  ]

Paketti: vt (0.57721+ds-3 ja muut)

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toolset for short variant discovery in genetic sequence data

vt is a variant tool set that discovers short variants from Next Generation Sequencing data.

Vt-normalize is a tool to normalize representation of genetic variants in the VCF. Variant normalization is formally defined as the consistent representation of genetic variants in an unambiguous and concise way. In vt a simple general algorithm to enforce this is implemented.

Muut pakettiin vt liittyvät paketit

  • depends
  • recommends
  • suggests
  • enhances

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Arkkitehtuuri Versio Paketin koko Koko asennettuna Tiedostot
s390x 0.57721+ds-3+b1 757.8 kt2,834.0 kt [tiedostoluettelo]