How to Install and Uninstall libvcflib2 Package on Kali Linux

Last updated: June 25,2024

1. Install "libvcflib2" package

Learn how to install libvcflib2 on Kali Linux

$ sudo apt update $ sudo apt install libvcflib2

2. Uninstall "libvcflib2" package

In this section, we are going to explain the necessary steps to uninstall libvcflib2 on Kali Linux:

$ sudo apt remove libvcflib2 $ sudo apt autoclean && sudo apt autoremove

3. Information about the libvcflib2 package on Kali Linux

Package: libvcflib2
Source: libvcflib
Version: 1.0.9+dfsg1-3
Installed-Size: 498
Maintainer: Debian Med Packaging Team
Architecture: amd64
Depends: libc6 (>= 2.33), libdisorder0 (>= 0.0.2), libfastahack0 (>= 0.0+git20160702.bbc645f), libgcc-s1 (>= 3.3.1), libsmithwaterman0 (>= 0.0+git20160702.2610e25), libstdc++6 (>= 13.1), libtabixpp0 (>= 1.0.0), libwfa2-0 (>= 2.3.3)
Size: 187976
SHA256: b2e5a28e51e6132aa5b8166e53c6391388c946f04a3f98a96b5b5ce06626d8fa
SHA1: 908faea3daed9e6a81c3852012eee025f2f2e287
MD5sum: d9d18b2fd84a4183d219e5ed07f6deac
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:
Multi-Arch: same
Homepage: https://github.com/vcflib/vcflib
Section: libs
Priority: optional
Filename: pool/main/libv/libvcflib/libvcflib2_1.0.9+dfsg1-3_amd64.deb