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The term paraphyly, or paraphyletic, derives from the two Ancient Greek words παρά (pará), meaning "beside, near", and φῦλον (phûlon), meaning "genus, species", [2] [3] and refers to the situation in which one or several monophyletic subgroups of organisms (e.g., genera, species) are left apart from all other descendants of a unique common ancestor.
These relationships are determined by phylogenetic inference methods that focus on observed heritable traits, such as DNA sequences, protein amino acid sequences, or morphology. The result of such an analysis is a phylogenetic tree—a diagram containing a hypothesis of relationships that reflects the evolutionary history of a group of ...
The result of these analyses is a phylogeny (also known as a phylogenetic tree) – a diagrammatic hypothesis about the history of the evolutionary relationships of a group of organisms. [6] Phylogenetic analyses have become central to understanding biodiversity, evolution, ecological genetics and genomes.
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It is a group of techniques within the larger fields of phylogenetics and genomics. Phylogenomics draws information by comparing entire genomes, or at least large portions of genomes. [3] Phylogenetics compares and analyzes the sequences of single genes, or a small number of genes, as well as many other types of data.
The science that tries to reconstruct phylogenetic trees and thus discover clades is called phylogenetics or cladistics, the latter term coined by Ernst Mayr (1965), derived from "clade". The results of phylogenetic/cladistic analyses are tree-shaped diagrams called cladograms; they, and all their branches, are phylogenetic hypotheses. [12]
Bayesian inference was introduced into molecular phylogenetics in the 1990s by three independent groups: Bruce Rannala and Ziheng Yang in Berkeley, [1] [2] Bob Mau in Madison, [3] and Shuying Li in University of Iowa, [4] the last two being PhD students at the time.
Symmetry invariants are non-phylogenetic in nature; they take on the expected value of zero regardless of the tree topology. However, it is possible to determine whether a particular multiple sequence alignment fits the Jukes-Cantor model of evolution (i.e., by testing whether the site patterns of the appropriate types are present in equal numbers).