How to Install and Uninstall trimmomatic Package on Ubuntu 20.10 (Groovy Gorilla)

Last updated: May 17,2024

1. Install "trimmomatic" package

Please follow the guidelines below to install trimmomatic on Ubuntu 20.10 (Groovy Gorilla)

$ sudo apt update $ sudo apt install trimmomatic

2. Uninstall "trimmomatic" package

Please follow the guidance below to uninstall trimmomatic on Ubuntu 20.10 (Groovy Gorilla):

$ sudo apt remove trimmomatic $ sudo apt autoclean && sudo apt autoremove

3. Information about the trimmomatic package on Ubuntu 20.10 (Groovy Gorilla)

Package: trimmomatic
Architecture: all
Version: 0.39+dfsg-1
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: 785
Depends: libjbzip2-java, default-jre
Filename: pool/universe/t/trimmomatic/trimmomatic_0.39+dfsg-1_all.deb
Size: 757492
MD5sum: de22b413dc5667b2f195bd37905eb987
SHA1: d80bb8f06a0a54e4c56d849653ea0d6edc0f86a2
SHA256: 6da915fa4372f7864f782be2454fd86668b522f877ba8b91f3c2674c560ff9de
SHA512: aa55103a09959a8e26d3c992ccbf390e865cc90a3c9081e0d2641d94c02f825a92bbaf53a0180de9eceda0bc79372cffa708e597ab54c997838f90ad75edf935
Homepage: http://www.usadellab.org/cms/index.php?page=trimmomatic
Description-en: flexible read trimming tool for Illumina NGS data
Trimmomatic performs a variety of useful trimming tasks for illumina
paired-end and single ended data.The selection of trimming steps and
their associated parameters are supplied on the command line.
.
The current trimming steps are:
* ILLUMINACLIP: Cut adapter and other illumina-specific sequences from
the read.
* SLIDINGWINDOW: Perform a sliding window trimming, cutting once thes
average quality within the window falls below a threshold.
* LEADING: Cut bases off the start of a read, if below a threshold quality
* TRAILING: Cut bases off the end of a read, if below a threshold quality
* CROP: Cut the read to a specified length
* HEADCROP: Cut the specified number of bases from the start of the read
* MINLENGTH: Drop the read if it is below a specified length
* TOPHRED33: Convert quality scores to Phred-33
* TOPHRED64: Convert quality scores to Phred-64
It works with FASTQ (using phred + 33 or phred + 64 quality scores,
depending on the Illumina pipeline used), either uncompressed or
gzipp'ed FASTQ. Use of gzip format is determined based on the .gz
extension.
Description-md5: fb8a901542618dcc98ce51bd3dfb107e