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From these studies an approximate time of divergence from the common ancestor of all modern human populations can be calculated.
It is clear that the variation in spindle organization in the bryophytes arose after divergence from the common ancestor.
It is also likely that they may possess different effective population size after the divergence from the common ancestor.
After divergence from the common ancestor, P. furiosus became adapted to the conditions of shallow water, whereas P. horikoshii and P. abyssi ancestor presumably remained in deep seas.
Bayesian and maximum likelihood phylogenies were in general agreement on systematic relationships and confirmed several 'orthology sets' of genes retained since divergence from the common ancestor.
By contrast, the observation that duplicated AtMYBs are orthologs of a single GmMYB gene suggested that the AtMYBs also experienced duplications after the divergence from the common ancestor.
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Under the MC model, the branches have the same length (1 1 ratio) because the divergence time from the common ancestor is obviously the same for both sister genomes.
We are interested in substitutions that occurred in the reference species since its divergence from the last common ancestor with the comparison species for example, on the human lineage after its last common ancestor with chimpanzee.
This indicates the divergence from the latest common ancestor of dermatophytes was later than the Aspergillus- Penicillium group.
Alternatively, the BCNV WWAV TAMV trichotomy may be the result of an essentially simultaneous divergence from the last common ancestor of the three North American arenaviruses.
This suggests that the innovation of RNA editing in dinoflagellates likely occurred after divergence from the alveolate common ancestor (fig. 3).
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