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

Last updated: November 06,2024

1. Install "python3-geneimpacts" package

Please follow the guidelines below to install python3-geneimpacts on Ubuntu 21.10 (Impish Indri)


    
        
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                sudo apt update
            
                    
    
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                sudo apt install
            
                        
                python3-geneimpacts
            
                    
    
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2. Uninstall "python3-geneimpacts" package

This is a short guide on how to uninstall python3-geneimpacts on Ubuntu 21.10 (Impish Indri):


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

Package: python3-geneimpacts
Architecture: all
Version: 0.3.7-3
Priority: optional
Section: universe/python
Source: python-geneimpacts
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 90
Depends: python3:any
Recommends: snpeff, bcftools
Filename: pool/universe/p/python-geneimpacts/python3-geneimpacts_0.3.7-3_all.deb
Size: 33544
MD5sum: 0ba80e0e440c4de9ecd1747ce92595b3
SHA1: b7614652df84a8844403c53064ebc1b4d30b0265
SHA256: 70315dd0962a1b3a55588393d5d955bf66f1b14b9c98f0f487d1edd759dec880
SHA512: a178b864f59ccac211926d3c0b1ace4c2ddfc517636ca889ffe8adb02c818c5495e6f9eea5641fa9fc37202f0c04d0a0209e959a05e76d2ffd9e67df481c31e4
Homepage: https://github.com/brentp/geneimpacts
Description-en: wraps command line tools to assess variants in gene sequences
Interpersonal differences in DNA is responsible for variations in
response to external stimuli, the efficiency of metabolism or
may even cause what is referenced as a genetic disorder.
.
A range of tools have been created to predict the importance of
differences (polymorphisms) in genetic sequences at single nucleotides,
SNPs. This Python class wraps and represents findings provided by any
of the tools snpEff, VEP and BCFT.
Description-md5: 5aa691288383fd64ae986ad138293a4c