How to Install and Uninstall blixem Package on Kali Linux

Last updated: October 05,2024

1. Install "blixem" package

Please follow the steps below to install blixem on Kali Linux


    
        
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                sudo apt update
            
                    
    
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                sudo apt install
            
                        
                blixem
            
                    
    
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2. Uninstall "blixem" package

This is a short guide on how to uninstall blixem on Kali Linux:


    
        
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                sudo apt remove
            
                        
                blixem
            
                    
    
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                sudo apt autoclean && sudo apt autoremove
            
                    
    
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3. Information about the blixem package on Kali Linux

Package: blixem
Source: seqtools (4.44.1+dfsg-7)
Version: 4.44.1+dfsg-7+b2
Installed-Size: 2248
Maintainer: Debian Med Packaging Team
Architecture: amd64
Depends: libc6 (>= 2.34), libcairo2 (>= 1.2.4), libcurl4 (>= 7.16.2), libgbtools0 (>= 4.44.1+dfsg), libgcc-s1 (>= 3.0), libglib2.0-0 (>= 2.35.9), libgtk2.0-0 (>= 2.14.0), libpango-1.0-0 (>= 1.14.0), libsqlite3-0 (>= 3.5.9), libstdc++6 (>= 5.2)
Size: 1390900
SHA256: 610fdeb040d5f5f80710bdb296a7f75414e370811be0b064a0d583d3292ddedb
SHA1: fbf2fdd8221d8d62132824e54000e971f205cb5c
MD5sum: fe7794da144213b142e47706071c96fb
Description: interactive browser of sequence alignments
Blixem is an interactive browser of sequence alignments that have been
stacked up in a "master-slave" multiple alignment; it is not a 'true'
multiple alignment but a 'one-to-many' alignment.
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* Overview section showing the positions of genes and alignments around
the alignment window
* Detail section showing the actual alignment of protein or nucleotide
sequences to the genomic DNA sequence.
* View alignments against both strands of the reference sequence.
* View sequences in nucleotide or protein mode; in protein mode, Blixem
will display the three-frame translation of the reference sequence.
* Residues are highlighted in different colours depending on whether
they are an exact match, conserved substitution or mismatch.
* Gapped alignments are supported, with insertions and deletions being
highlighted in the match sequence.
* Matches can be sorted and filtered.
* SNPs and other variations can be highlighted in the reference
sequence.
* Poly(A) tails can be displayed and poly(A) signals highlighted in the
reference sequence.
Description-md5:
Homepage: https://www.sanger.ac.uk/science/tools/seqtools
Tag: uitoolkit::gtk
Section: science
Priority: optional
Filename: pool/main/s/seqtools/blixem_4.44.1+dfsg-7+b2_amd64.deb