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Step 3. Construction of the phylogenetic tree Distance methods
Step 3. Construction of the phylogenetic tree Distance methods

... P = the fraction of sequence positions differing by a transition Q = the fraction of sequence positions differing by a transversion. ...
Chapter 20 Questions
Chapter 20 Questions

... Suppose that species 1 and species 3 have similar appearances but very divergent gene sequences. Species 2 and species 3 have very different appearances but similar gene sequences. Which pair of species is more likely to be closely related: 1 and 2, or 2 and 3? Explain. ...
3000_2013_1e
3000_2013_1e

... • when and how were complex eyes evolved? in what species are they lost? are the genes required to develop eyes still there? can they be expressed in different ways? ...
tree
tree

... • Can only work for pairs of sequences that are similar enough to be aligned • All base changes are considered equal • Insertion/deletions are generally given a larger weight than replacements (gap penalties). • Possible to correct for multiple substitutions at a single site, which is common in dist ...
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Maximum parsimony (phylogenetics)

In phylogenetics, maximum parsimony is an optimality criterion under which the phylogenetic tree that minimizes the total number of character-state changes is to be preferred. Under the maximum-parsimony criterion, the optimal tree will minimize the amount of homoplasy (i.e., convergent evolution, parallel evolution, and evolutionary reversals). In other words, under this criterion, the shortest possible tree that explains the data is considered best. The principle is akin to Occam's razor, which states that—all else being equal—the simplest hypothesis that explains the data should be selected. Some of the basic ideas behind maximum parsimony were presented by James S. Farris in 1970 and Walter M. Fitch in 1971.Maximum parsimony is an intuitive and simple criterion, and it is popular for this reason. However, although it is easy to score a phylogenetic tree (by counting the number of character-state changes), there is no algorithm to quickly generate the most-parsimonious tree. Instead, the most-parsimonious tree must be found in ""tree space"" (i.e., amongst all possible trees). For a small number of taxa (i.e., less than nine) it is possible to do an exhaustive search, in which every possible tree is scored, and the best one is selected. For nine to twenty taxa, it will generally be preferable to use branch-and-bound, which is also guaranteed to return the best tree. For greater numbers of taxa, a heuristic search must be performed.Because the most-parsimonious tree is always the shortest possible tree, this means that—in comparison to the ""true"" tree that actually describes the evolutionary history of the organisms under study—the ""best"" tree according to the maximum-parsimony criterion will often underestimate the actual evolutionary change that has occurred. In addition, maximum parsimony is not statistically consistent. That is, it is not guaranteed to produce the true tree with high probability, given sufficient data. As demonstrated in 1978 by Joe Felsenstein, maximum parsimony can be inconsistent under certain conditions, such as long-branch attraction.
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