Recently I needed to investigate sequence conservation for a project, and found that there was no easy-to-use script to generate conservation scores for a list of sequences.
The code is posted as a gist here: https://gist.github.com/atc3/f0260a99c5328a12f4b6fbbe65beec83, as a python function and a CSV file for the PET91 substitution matrix (Thanks to @ACRMGroup for digitizing it).
The conservation function I’m using is the “Valdar conservation score” described in Valdar and Thornton, 2001. It’s written from scratch and validated by checking the output on the same set of sequences when compared to the same Valdar score generated in SnapGene Viewer. Input a list of aligned sequences (I’m using Clustal Omega for multiple sequence alignment), and the function returns a list of conservation scores - one for each base in the alignment. The score is scaled from 0 to 1, where 0 is not conserved at all, and 1 is perfectly conserved.
I’ve split up the code into some general parts so it should be simple to use a different substitution matrix (BLOSUM, etc) or a different amino acid similarity function entirely.
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