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Basically, the whole algorthm is independent of sequence type if a proper pairwise alignment algorithm and score is used. Therefore, it should be possible to run the same algorithm with protein sequences. I expect it to be somewhat slower than for nucleotide sequences because we cannot use the ultra-fast edit-score alignment algorithm in SeqAn.
The text was updated successfully, but these errors were encountered:
Basically, the whole algorthm is independent of sequence type if a proper pairwise alignment algorithm and score is used. Therefore, it should be possible to run the same algorithm with protein sequences. I expect it to be somewhat slower than for nucleotide sequences because we cannot use the ultra-fast edit-score alignment algorithm in SeqAn.
The text was updated successfully, but these errors were encountered: