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The best evolutionary model for each of the selected partitions was simultaneously estimated in the same software.
The best evolutionary model for each of the sequenced genes were the six parameter general time reversible (GTR) model of nucleotide substitution (nst = 6, rates = invgamma).
The best evolutionary model for sequences derived from each patient included a class allowing for positively selected codons (ω>1) in 18 of the 22 analyzed patients (Table 3).
Version 3.06 of Modeltest [25] was used in conjunction with PAUP* 4.0 [26] to estimate the best evolutionary model for the construction of each maximum likelihood (ML) tree using the Akaike Information Criterion [27].
The best evolutionary model for the ML analysis was selected by the ProtTest [ 52].
ProtTest 2.4 (Abascal et al. 2005) was used to select the best evolutionary model for our data.
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The best evolutionary models for the analyzed amino-acids data set were rtREV based on the Akaike Information Criterion (AIC) [ 68] and Blosum62 based on Bayesian Information Criterion (BIC) [ 69].
The best evolutionary model of nucleotide substitution was determined using jModelTest 0.1.1 [ 102].
The best evolutionary model determined for the sequences was TrN + I + G.
The best evolutionary model was estimated for each alignment using MEGA5 software [ 67].
For both the 12S and 16S datasets, the best evolutionary model was GTR+I+G, whereas for the cytB fragment, it was TIM2+I+G.
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