I was wondering how I might be able to use the BioPython package to extract nucleotide frequencies over an aligned set of sequences. Does anybody know how I might be able to do this? I am assuming that I have aligned sequences, including the appropriate spacers at places where base pair deletions have occurred.
Is there a single function in the BioPython package that allows me to do that? I've tried browsing through the API, but I haven't been able to find anything. (It might be I'm not looking at it correctly, or that the terminology used is different, perhaps?)
2 answers
did you tried this Bio.Align.AlignInfo.Summary Calculate summary info about the alignment.
This class should be used to caclculate information summarizing the results of an alignment. This may either be straight consensus info or more complicated things.
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