[ 原始碼： vt ]
套件：vt（0.57721+ds-3 以及其他的）
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.
其他與 vt 有關的套件
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- dep: libc6 (>= 2.34)
- GNU C 函式庫：共用函式庫
同時作為一個虛擬套件由這些套件填實： libc6-udeb
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- dep: libgcc-s1 (>= 3.0)
- GCC 支援函式庫
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- dep: libhts3t64 (>= 1.17)
- C library for high-throughput sequencing data formats
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- dep: libpcre2-8-0 (>= 10.22)
- New Perl Compatible Regular Expression Library- 8 bit runtime files
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- dep: libstdc++6 (>= 13.1)
- GNU Standard C++ Library v3
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- dep: r-base-core
- GNU R core of statistical computation and graphics system