パッケージ: libvcflib-tools (1.0.2+dfsg-2)
libvcflib-tools に関するリンク
Debian の資源:
libvcflib ソースパッケージをダウンロード:
- [libvcflib_1.0.2+dfsg-2.dsc]
- [libvcflib_1.0.2+dfsg.orig.tar.xz]
- [libvcflib_1.0.2+dfsg-2.debian.tar.xz]
メンテナ:
外部の資源:
- ホームページ [github.com]
類似のパッケージ:
C++ library for parsing and manipulating VCF files (tools)
The Variant Call Format (VCF) is a flat-file, tab-delimited textual format intended to concisely describe reference-indexed variations between individuals. VCF provides a common interchange format for the description of variation in individuals and populations of samples, and has become the defacto standard reporting format for a wide array of genomic variant detectors.
vcflib provides methods to manipulate and interpret sequence variation as it can be described by VCF. It is both:
* an API for parsing and operating on records of genomic variation as it can be described by the VCF format, * and a collection of command-line utilities for executing complex manipulations on VCF files.
This package contains several tools using the library.
その他の libvcflib-tools 関連パッケージ
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- dep: libc6 (>= 2.29)
- GNU C ライブラリ: 共有ライブラリ
以下のパッケージによって提供される仮想パッケージでもあります: libc6-udeb
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- dep: libfastahack0 (>= 1.0.0+dfsg)
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- GCC 共有ライブラリ
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- dep: libsmithwaterman0 (>= 0.0+git20160702.2610e25)
- determine similar regions between two strings or genomic sequences (lib)
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- dep: libstdc++6 (>= 5.2)
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- dep: libtabixpp0 (>= 1.0.0)
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- dep: libvcflib1 (>= 1.0.2+dfsg)
- C++ library for parsing and manipulating VCF files
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- dep: r-base-core
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- dep: r-cran-ggplot2
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- dep: r-cran-gridbase
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