How to Install and Uninstall python3-htseq Package on Ubuntu 21.10 (Impish Indri)

Last updated: May 21,2024

1. Install "python3-htseq" package

Please follow the step by step instructions below to install python3-htseq on Ubuntu 21.10 (Impish Indri)


    
        
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                sudo apt update
            
                    
    
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            $
        

        
            
                sudo apt install
            
                        
                python3-htseq
            
                    
    
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2. Uninstall "python3-htseq" package

Please follow the guidance below to uninstall python3-htseq on Ubuntu 21.10 (Impish Indri):


    
        
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                sudo apt remove
            
                        
                python3-htseq
            
                    
    
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                sudo apt autoclean && sudo apt autoremove
            
                    
    
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3. Information about the python3-htseq package on Ubuntu 21.10 (Impish Indri)

Package: python3-htseq
Architecture: amd64
Version: 0.13.5-1
Priority: optional
Section: universe/python
Source: htseq
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 787
Provides: python-htseq
Depends: python3 (<< 3.10), python3 (>= 3.9~), python3-numpy, python3-pysam, python3:any, libc6 (>= 2.14), libgcc-s1 (>= 3.0), libstdc++6 (>= 5)
Breaks: python-htseq (<= 0.9.1)
Filename: pool/universe/h/htseq/python3-htseq_0.13.5-1_amd64.deb
Size: 220948
MD5sum: 4434d33300210ce195da4f542ee999c0
SHA1: f9631c77040357e2a46ae3c60efe0e1bfac27982
SHA256: 50d28f804a120a6a1b542640959f230fe99abbd938045ce4c7b5007a5c7f6d3b
SHA512: 41a719bae3afdad3cd96cf8fb7bbe8be7c34201bb4457f1d4e94dac240c350f777e16e6a1a4dfe3e8f061af8cce6db77cf33427580e1c2ed69b8588b16ff6f14
Homepage: https://www-huber.embl.de/users/anders/HTSeq/doc/overview.html
Description-en: Python3 high-throughput genome sequencing read analysis utilities
HTSeq can be used to performing a number of common analysis tasks
when working with high-throughput genome sequencing reads:
.
* Getting statistical summaries about the base-call quality scores to
study the data quality.
* Calculating a coverage vector and exporting it for visualization in
a genome browser.
* Reading in annotation data from a GFF file.
* Assigning aligned reads from an RNA-Seq experiments to exons and
genes.
.
This package contains the Python 3 module.
Description-md5: ffe5034bc59f88e9b8ed360ec7976622