How to Install and Uninstall artfastqgenerator-examples Package on Ubuntu 20.10 (Groovy Gorilla)
Last updated: December 26,2024
1. Install "artfastqgenerator-examples" package
Please follow the guidelines below to install artfastqgenerator-examples on Ubuntu 20.10 (Groovy Gorilla)
$
sudo apt update
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$
sudo apt install
artfastqgenerator-examples
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2. Uninstall "artfastqgenerator-examples" package
Please follow the guidelines below to uninstall artfastqgenerator-examples on Ubuntu 20.10 (Groovy Gorilla):
$
sudo apt remove
artfastqgenerator-examples
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the artfastqgenerator-examples package on Ubuntu 20.10 (Groovy Gorilla)
Package: artfastqgenerator-examples
Architecture: all
Version: 0.0.20150519-3
Priority: optional
Section: universe/science
Source: artfastqgenerator
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 1271
Filename: pool/universe/a/artfastqgenerator/artfastqgenerator-examples_0.0.20150519-3_all.deb
Size: 1292620
MD5sum: fbb1eb265e0b1c12b8f40fe4ed8bf373
SHA1: 62e4692842d1b6a94fd43dc783e55d29c2183315
SHA256: 8adf2e260f52f7dc9c9fc082d582afbd38b5db7ccc1dbdbf95697aa8cf51f752
SHA512: 16328a648da9f1a30c84409733f766ed2a764884e10d7d7efcdcd3db28c5f6ebdcb216ecdd713bd482c450436f40bbd67ffe2de8f6c894c28d83db9aad2eea78
Homepage: https://sourceforge.net/projects/artfastqgen/
Description-en: ou7puts artificial FASTQ files derived from a reference genome (examples)
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 example data for artfastqgenerator.
Description-md5: d7d2bac937254bc53677ebfece5aeb33
Architecture: all
Version: 0.0.20150519-3
Priority: optional
Section: universe/science
Source: artfastqgenerator
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 1271
Filename: pool/universe/a/artfastqgenerator/artfastqgenerator-examples_0.0.20150519-3_all.deb
Size: 1292620
MD5sum: fbb1eb265e0b1c12b8f40fe4ed8bf373
SHA1: 62e4692842d1b6a94fd43dc783e55d29c2183315
SHA256: 8adf2e260f52f7dc9c9fc082d582afbd38b5db7ccc1dbdbf95697aa8cf51f752
SHA512: 16328a648da9f1a30c84409733f766ed2a764884e10d7d7efcdcd3db28c5f6ebdcb216ecdd713bd482c450436f40bbd67ffe2de8f6c894c28d83db9aad2eea78
Homepage: https://sourceforge.net/projects/artfastqgen/
Description-en: ou7puts artificial FASTQ files derived from a reference genome (examples)
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 example data for artfastqgenerator.
Description-md5: d7d2bac937254bc53677ebfece5aeb33