How to Install and Uninstall pirs-examples Package on Ubuntu 21.10 (Impish Indri)

Last updated: April 19,2024

1. Install "pirs-examples" package

Please follow the guidelines below to install pirs-examples on Ubuntu 21.10 (Impish Indri)

$ sudo apt update $ sudo apt install pirs-examples

2. Uninstall "pirs-examples" package

This tutorial shows how to uninstall pirs-examples on Ubuntu 21.10 (Impish Indri):

$ sudo apt remove pirs-examples $ sudo apt autoclean && sudo apt autoremove

3. Information about the pirs-examples package on Ubuntu 21.10 (Impish Indri)

Package: pirs-examples
Architecture: all
Version: 2.0.2+dfsg-9
Priority: optional
Section: universe/science
Source: pirs
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 1913
Filename: pool/universe/p/pirs/pirs-examples_2.0.2+dfsg-9_all.deb
Size: 1945376
MD5sum: 0e7c8c9a228cfd5a733b81066e6cdb21
SHA1: 2bcce6e14d489484f1ec8d66867d41f69ba6733d
SHA256: 798e0803cb581a862c097b7d42ea59a9f74534c337800d59a2a2381b592f803d
SHA512: ff3b8ab27db85a7be691c8fd31502bfad4c038e389e1383d02887b1f2391ba720bfb6da1eea356b7247ccd242567cb0e260f752429c23339490dc669a9ede88d
Homepage: https://github.com/galaxy001/pirs
Description-en: profile basd Illumina pair-end Reads Simulator (example data)
The program pIRS can be used for simulating Illumina PE reads, with a
series of characters generated by Illumina sequencing platform, such as
insert size distribution, sequencing error(substitution, insertion,
deletion), quality score and GC content-coverage bias.
.
The insert size follows a normal distribution, so users should set the
mean value and standard deviation. Usually the standard deviation is set
as 1/20 of the mean value. The normal distribution by Box-Muller method
is simulated.
.
The program simulates sequencing error, quality score and GC content-
coverage bias according to the empirical distribution profile. Some
default profiles counted from lots of real sequencing data are provided.
.
To simulate reads from diploid genome, users should simulate the diploid
genome sequence firstly by setting the ratio of heterozygosis SNP,
heterozygosis InDel and structure variation.
.
This package contains some example data.
Description-md5: 68f36220abe2489f38bb06b1e2f43810