[ 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
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- 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
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- dep: libgcc-s1 (>= 3.0) [除 armel, armhf]
- GCC 支持库
- dep: libgcc-s1 (>= 3.5) [armel, armhf]
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- dep: libhts3 (>= 1.10)
- 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 (>= 5.2)
- GNU 标准 C++ 库,第3版
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- dep: r-base-core
- GNU R core of statistical computation and graphics system
下载 vt
硬件架构 | 软件包大小 | 安装后大小 | 文件 |
---|---|---|---|
amd64 | 756.2 kB | 2,565.0 kB | [文件列表] |
arm64 | 624.3 kB | 2,241.0 kB | [文件列表] |
armel | 604.2 kB | 2,152.0 kB | [文件列表] |
armhf | 624.4 kB | 1,524.0 kB | [文件列表] |
i386 | 763.0 kB | 2,776.0 kB | [文件列表] |
mips64el | 576.1 kB | 3,225.0 kB | [文件列表] |
mipsel | 580.6 kB | 2,977.0 kB | [文件列表] |
ppc64el | 693.5 kB | 2,833.0 kB | [文件列表] |
s390x | 638.5 kB | 2,533.0 kB | [文件列表] |