Package: vt-examples (0.57721+ds-3)
Links for vt-examples
Download Source Package vt:
- Debian Med Packaging Team (Mail Archive)
- Antoni Villalonga
- Homepage [genome.sph.umich.edu]
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.
Other Packages Related to vt-examples
- enh: vt
- toolset for short variant discovery in genetic sequence data