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The evolutionary genetic distances (expressed in terms of the number of differences per 100 bases or amino acids, including length polymorphisms) between every pair of sequences in a multiple alignment were generated using the DISTMAT program accessible at http://hpc.ilri.cgiar.org/emboss/ [36].
Thus, all sequences in the resulted multiple alignment were less than 65% identical with each other.
Nonconserved regions in each multiple alignment were removed using an in-house script.
Values for multiple alignment were gap opening penalty 15, gap extension penalty 0.3, and delay divergent sequences 25%.
A few manual adjustments to the multiple alignment were made before running Gblocks, which yielded 1,679 positions.
After gap removal all families with less than 25% or more than 98% identical nucleotide positions in the multiple alignment were filtered out.
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The goal of multiple alignment is to align sequences according to their evolutionary relationships.
For each DNA sequence, a multiple alignment was created by Clustal W Thompsonn et al. 1994).
Multiple alignment was constructed with CLUSTALW [26].
A multiple alignment was achieved within each GH family.
Multiple alignment was done with ClustalX2 under default settings.
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