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[ Bron: vt  ]

Pakket: vt (0.57721+ds-3)

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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.

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s390x 638,5 kB2.533,0 kB [overzicht]