[ ソース: vt ]
パッケージ: vt-examples (0.57721+ds-3)
vt-examples に関するリンク
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外部の資源:
- ホームページ [genome.sph.umich.edu]
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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.
その他の vt-examples 関連パッケージ
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- enh: vt
- toolset for short variant discovery in genetic sequence data