Paket: vt (0.57721+ds-3 och andra)

[ Källkod: vt  ]

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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Hämta vt

Hämtningar för alla tillgängliga arkitekturer

Arkitektur	Version	Paketstorlek	Installerad storlek	Filer
armhf	0.57721+ds-3+b1	657,9 kbyte	1.661,0 kbyte	[filförteckning]