[ Bron: vt ]
Pakket: vt-examples (0.57721+ds-3)
Verwijzigingen voor vt-examples
Debian bronnen:
Het bronpakket vt downloaden:
Beheerders:
Externe bronnen:
- Homepage [genome.sph.umich.edu]
Vergelijkbare pakketten:
toolset for short variant discovery in genetic sequence data (examples)
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.
This package contains some example data.
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- enh: vt
- toolset for short variant discovery in genetic sequence data