How to Install and Uninstall artfastqgenerator-doc Package on Ubuntu 20.10 (Groovy Gorilla)
Last updated: February 08,2025
1. Install "artfastqgenerator-doc" package
Please follow the steps below to install artfastqgenerator-doc on Ubuntu 20.10 (Groovy Gorilla)
$
sudo apt update
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$
sudo apt install
artfastqgenerator-doc
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2. Uninstall "artfastqgenerator-doc" package
This is a short guide on how to uninstall artfastqgenerator-doc on Ubuntu 20.10 (Groovy Gorilla):
$
sudo apt remove
artfastqgenerator-doc
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the artfastqgenerator-doc package on Ubuntu 20.10 (Groovy Gorilla)
Package: artfastqgenerator-doc
Architecture: all
Version: 0.0.20150519-3
Priority: optional
Section: universe/doc
Source: artfastqgenerator
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 525
Filename: pool/universe/a/artfastqgenerator/artfastqgenerator-doc_0.0.20150519-3_all.deb
Size: 40432
MD5sum: f54002051fc542debbb11074e7d33413
SHA1: 23f16fcd85e9e1207afa2426efe94536a89d2b5b
SHA256: ad089558d2a1242effed24989b284d631c5baa98491be0c5d43654b925fb88f9
SHA512: 77317108803851dbb4e20d0fefe484d8877b6f9791a7822f7c99e7a1fbc4a8dc2bba589618c4054b83f3a79b8f5968105ba9526172c76da5f0179578c140a2b0
Homepage: https://sourceforge.net/projects/artfastqgen/
Description-en: outputs artificial FASTQ files derived from a reference genome (doc)
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.
.
This package contains the Java API documentation for artfastqgenerator.
Description-md5: a4aad7fd5379ce482d945d65185407e3
Architecture: all
Version: 0.0.20150519-3
Priority: optional
Section: universe/doc
Source: artfastqgenerator
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 525
Filename: pool/universe/a/artfastqgenerator/artfastqgenerator-doc_0.0.20150519-3_all.deb
Size: 40432
MD5sum: f54002051fc542debbb11074e7d33413
SHA1: 23f16fcd85e9e1207afa2426efe94536a89d2b5b
SHA256: ad089558d2a1242effed24989b284d631c5baa98491be0c5d43654b925fb88f9
SHA512: 77317108803851dbb4e20d0fefe484d8877b6f9791a7822f7c99e7a1fbc4a8dc2bba589618c4054b83f3a79b8f5968105ba9526172c76da5f0179578c140a2b0
Homepage: https://sourceforge.net/projects/artfastqgen/
Description-en: outputs artificial FASTQ files derived from a reference genome (doc)
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.
.
This package contains the Java API documentation for artfastqgenerator.
Description-md5: a4aad7fd5379ce482d945d65185407e3