[ 原始碼： vt ]
套件：vt-examples（0.57721+ds-3）
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.
其他與 vt-examples 有關的套件
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- enh: vt
- toolset for short variant discovery in genetic sequence data