How to Install and Uninstall mosdepth-examples Package on Ubuntu 22.04 LTS (Jammy Jellyfish)

Last updated: May 08,2024

1. Install "mosdepth-examples" package

Please follow the instructions below to install mosdepth-examples on Ubuntu 22.04 LTS (Jammy Jellyfish)

$ sudo apt update $ sudo apt install mosdepth-examples

2. Uninstall "mosdepth-examples" package

In this section, we are going to explain the necessary steps to uninstall mosdepth-examples on Ubuntu 22.04 LTS (Jammy Jellyfish):

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

3. Information about the mosdepth-examples package on Ubuntu 22.04 LTS (Jammy Jellyfish)

Package: mosdepth-examples
Architecture: all
Version: 0.3.2+ds-1
Multi-Arch: foreign
Priority: optional
Section: universe/science
Source: mosdepth
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 1038
Filename: pool/universe/m/mosdepth/mosdepth-examples_0.3.2+ds-1_all.deb
Size: 1034760
MD5sum: 53d13aa68cb93f3018db08bd6b6e7131
SHA1: 092639896ffe6cbf08031da04c8c879f24619ca0
SHA256: f7a71c4514bc04875f2a3d2341c8c4f753a91e27bbdb8488feb7dcf4f7d4d5cc
SHA512: 617cd0a400f62616fd8e234592c3856693b0d4627c807a4840bee63533e68368e46763d170fb106832acc8e1ecf774112219bf1d4a521f24af9aa7f2b5622e64
Homepage: https://github.com/brentp/mosdepth
Description-en: Test data for mosdepth
Many small reads are produced by high-throughput "next generation"
sequencing technologies. The final sequence is derived from how
these reads are overlapping towards a consensus.
The more reads are covering/confirming parts of a nucleotide seq,
the higher the confidence is. Too many reads would be indicative
of e.g. repeats in the genome.
.
mosdepth can output:
* per-base depth about 2x as fast samtools depth--about 25 minutes
of CPU time for a 30X genome.
* mean per-window depth given a window size--as would be used for
CNV calling.
* the mean per-region given a BED file of regions.
* a distribution of proportion of bases covered at or above a given
threshold for each chromosome and genome-wide.
* quantized output that merges adjacent bases as long as they fall
in the same coverage bins e.g. (10-20)
* threshold output to indicate how many bases in each region are
covered at the given thresholds.
when appropriate, the output files are bgzipped and indexed for ease
of use.
.
This package contains a test data set as well as sample scripts
running some test suite provided by Debian also as autopkgtest.
Description-md5: 898808e2e4cef87b5990e435edecc708