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[ Source: vt  ]

Package: 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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Architecture Package Size Installed Size Files
amd64 756.2 kB2,565.0 kB [list of files]
arm64 624.3 kB2,241.0 kB [list of files]
armel 604.2 kB2,152.0 kB [list of files]
armhf 624.4 kB1,524.0 kB [list of files]
i386 763.0 kB2,776.0 kB [list of files]
mips64el 576.1 kB3,225.0 kB [list of files]
mipsel 580.6 kB2,977.0 kB [list of files]
ppc64el 693.5 kB2,833.0 kB [list of files]
s390x 638.5 kB2,533.0 kB [list of files]