How to Install and Uninstall libvcflib1 Package on Kali Linux
Last updated: November 05,2024
Deprecated! Installation of this package may no longer be supported.
1. Install "libvcflib1" package
Please follow the guidelines below to install libvcflib1 on Kali Linux
$
sudo apt update
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$
sudo apt install
libvcflib1
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2. Uninstall "libvcflib1" package
Learn how to uninstall libvcflib1 on Kali Linux:
$
sudo apt remove
libvcflib1
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the libvcflib1 package on Kali Linux
Package: libvcflib1
Source: libvcflib
Version: 1.0.3+dfsg-1
Installed-Size: 417
Maintainer: Debian Med Packaging Team
Architecture: amd64
Depends: libc6 (>= 2.29), libdisorder0 (>= 0.0.2), libfastahack0 (>= 0.0+git20160702.bbc645f), libgcc-s1 (>= 3.0), libsmithwaterman0 (>= 0.0+git20160702.2610e25), libstdc++6 (>= 11), libtabixpp0 (>= 1.0.0)
Size: 152300
SHA256: f35abd921415dcf6ba85cdb5a18a9d917f0b8074e48a8e9031001e25b87d445c
SHA1: 8fadc94318119ab4a2eaa9fae30c3d54d7112d50
MD5sum: 579917343f4310792529f726fe9d11f8
Description: C++ library for parsing and manipulating VCF files
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.
Description-md5: 4a37be6058b4cb297a5550cbccc89a50
Multi-Arch: same
Homepage: https://github.com/vcflib/vcflib
Tag: role::shared-lib
Section: libs
Priority: optional
Filename: pool/main/libv/libvcflib/libvcflib1_1.0.3+dfsg-1_amd64.deb
Source: libvcflib
Version: 1.0.3+dfsg-1
Installed-Size: 417
Maintainer: Debian Med Packaging Team
Architecture: amd64
Depends: libc6 (>= 2.29), libdisorder0 (>= 0.0.2), libfastahack0 (>= 0.0+git20160702.bbc645f), libgcc-s1 (>= 3.0), libsmithwaterman0 (>= 0.0+git20160702.2610e25), libstdc++6 (>= 11), libtabixpp0 (>= 1.0.0)
Size: 152300
SHA256: f35abd921415dcf6ba85cdb5a18a9d917f0b8074e48a8e9031001e25b87d445c
SHA1: 8fadc94318119ab4a2eaa9fae30c3d54d7112d50
MD5sum: 579917343f4310792529f726fe9d11f8
Description: C++ library for parsing and manipulating VCF files
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.
Description-md5: 4a37be6058b4cb297a5550cbccc89a50
Multi-Arch: same
Homepage: https://github.com/vcflib/vcflib
Tag: role::shared-lib
Section: libs
Priority: optional
Filename: pool/main/libv/libvcflib/libvcflib1_1.0.3+dfsg-1_amd64.deb