How to Install and Uninstall artfastqgenerator Package on Ubuntu 21.04 (Hirsute Hippo)

Last updated: November 25,2024

1. Install "artfastqgenerator" package

Learn how to install artfastqgenerator on Ubuntu 21.04 (Hirsute Hippo)


    
        
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                sudo apt update
            
                    
    
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                sudo apt install
            
                        
                artfastqgenerator
            
                    
    
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2. Uninstall "artfastqgenerator" package

This guide let you learn how to uninstall artfastqgenerator on Ubuntu 21.04 (Hirsute Hippo):


    
        
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                sudo apt remove
            
                        
                artfastqgenerator
            
                    
    
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                sudo apt autoclean && sudo apt autoremove
            
                    
    
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3. Information about the artfastqgenerator package on Ubuntu 21.04 (Hirsute Hippo)

Package: artfastqgenerator
Architecture: all
Version: 0.0.20150519-4
Priority: optional
Section: universe/science
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 56
Depends: default-jre
Filename: pool/universe/a/artfastqgenerator/artfastqgenerator_0.0.20150519-4_all.deb
Size: 40620
MD5sum: b90d601555405961f435e595148394f1
SHA1: 41e2f05a69962a9c8c6e5e2afe02c5fe71d4b162
SHA256: fdf87f1db6ed9dc01d55fcc41d919500407b85ba6ad75f12369ae92277356d0d
SHA512: 0cc0d235af7b4edb01e2b918beb09409fff27121daaf043a3481bad6bca58b3e934037dd02d65b7db49af6fbf595697da05aaf6e4b6f339d2e21579e08abb502
Homepage: https://sourceforge.net/projects/artfastqgen/
Description-en: outputs artificial FASTQ files derived from a reference genome
ArtificialFastqGenerator takes the reference genome (in FASTA format) as
input and outputs artificial FASTQ files in the Sanger format. It can
accept Phred base quality scores from existing FASTQ files, and use them
to simulate sequencing errors. Since the artificial FASTQs are derived
from the reference genome, the reference genome provides a gold-standard
for calling variants (Single Nucleotide Polymorphisms (SNPs) and
insertions and deletions (indels)). This enables evaluation of a Next
Generation Sequencing (NGS) analysis pipeline which aligns reads to the
reference genome and then calls the variants.
Description-md5: 46c5205dd3fb030f1a4090e0bf9cf921