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The average divergence between these STs was approximately 0.5%, and the maximum divergence, between STs 1850 and 1223, was 0.94%.
As the clustering threshold increases up to the maximum divergence between alleles, oversplit allelic clusters are collapsed, decreasing the proportion of 1-haplotype clusters, with a concomitant increase in 2-haplotype clusters.
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In the present work, we perform a theoretical analysis of the focusing properties of neutron beams, and validate them using a combination of Monte-Carlo simulations and Particle Swarm Optimisations (PSOs), where there is a close correspondence between the maximum divergence of the beam and the shape of the guide.
The maximum divergence in these estimations was observed between the topologies obtaining after leaving out the Cryptotis (9 Ma) and Otisorex (3.5 Ma) calibration points, respectively.
The maximum divergence of nucleotide sequences in lineage 2 (18.9%) was between a bird isolate from Madagascar AnMg 798 and several South African isolates from humans and mosquitoes.
The average nucleotide divergence between orthologous genes in MSHR1132 and typical S. aureus is approximately sevenfold greater than the maximum divergence observed in this species to date.
The maximum half angle of rotation is the maximum divergence in one direction from the midline.
The minimum divergence among MOTU exceeded the maximum divergence of 2.9% within MOTU.
This suggests minimum and maximum divergence between F. orientalis and F. sylvatica of about 1.7 million and 5.74 million years BP (Table 2).
When simulations were started using maximum divergence between chromosome arrangements (i.e. each chromosome arrangement was fixed for a different allele), differences were either non-significant or there was higher genetic diversity in the inverted chromosomes.
Pair-wise FST values among these four sub-populations indicated maximum divergence between indica and japonica (FST = 0.89) and minimum between aromatics and japonica (0.28) (see Additional file 5).
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