How to Install and Uninstall python-htseq Package on Ubuntu 16.04 LTS (Xenial Xerus)

Last updated: November 07,2024

1. Install "python-htseq" package

This tutorial shows how to install python-htseq on Ubuntu 16.04 LTS (Xenial Xerus)


    
        
            $
        

        
            
                sudo apt update
            
                    
    
    Copied


    
        
            $
        

        
            
                sudo apt install
            
                        
                python-htseq
            
                    
    
    Copied

2. Uninstall "python-htseq" package

Please follow the step by step instructions below to uninstall python-htseq on Ubuntu 16.04 LTS (Xenial Xerus):


    
        
            $
        

        
            
                sudo apt remove
            
                        
                python-htseq
            
                    
    
    Copied


    
        
            $
        

        
            
                sudo apt autoclean && sudo apt autoremove
            
                    
    
    Copied

3. Information about the python-htseq package on Ubuntu 16.04 LTS (Xenial Xerus)

Package: python-htseq
Priority: optional
Section: universe/python
Installed-Size: 660
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Architecture: amd64
Source: htseq
Version: 0.5.4p3-2
Depends: python (>= 2.7), python (<< 2.8), python:any (>= 2.7.1-0ubuntu2), libc6 (>= 2.14), libgcc1 (>= 1:4.1.1), libstdc++6 (>= 4.1.1)
Filename: pool/universe/h/htseq/python-htseq_0.5.4p3-2_amd64.deb
Size: 203960
MD5sum: c6a08a6f6b15732218521c923c668504
SHA1: 9421082d51fea58c0f5f30e312a2fc7fa0b9798f
SHA256: 9713af0d370c120ec06c8a15d8937c3252f8aecdc6a91a5f56b9fc3f86af04c3
Description-en: 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.
Description-md5: a43a27b81784df2c65d60fc408d9aa0b
Homepage: http://www-huber.embl.de/users/anders/HTSeq/doc/overview.html
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Origin: Ubuntu