[ 源代码： vt ]
软件包：vt（0.57721+ds-3）
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.
其他与 vt 有关的软件包
|
|
|
|
-
- dep: libc6 (>= 2.29)
- GNU C 语言运行库：共享库
同时作为一个虚包由这些包填实： libc6-udeb
-
- dep: libgcc-s1 (>= 3.0)
- GCC 支持库
-
- dep: libhts3 (>= 1.10)
- C library for high-throughput sequencing data formats
-
- dep: libpcre2-8-0 (>= 10.22)
- New Perl Compatible Regular Expression Library- 8 bit runtime files
-
- dep: libstdc++6 (>= 5.2)
- GNU 标准 C++ 库，第3版
-
- dep: r-base-core
- GNU R core of statistical computation and graphics system