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  2. Tajima's D - Wikipedia

    en.wikipedia.org/wiki/Tajima's_D

    Tajima's D is a population genetic test statistic created by and named after the Japanese researcher Fumio Tajima. [1] Tajima's D is computed as the difference between two measures of genetic diversity: the mean number of pairwise differences and the number of segregating sites, each scaled so that they are expected to be the same in a neutrally evolving population of constant size.

  3. Ka/Ks ratio - Wikipedia

    en.wikipedia.org/wiki/Ka/Ks_ratio

    Thus "long branches" in a dN/dS analysis can lead to underestimates of both dN and dS, and the longer the branch, the harder it is to correct for the introduced noise. [3] Of course, the ancestral sequence is usually unknown, and two lineages being compared will have been evolving in parallel since their last common ancestor.

  4. Fumio Tajima - Wikipedia

    en.wikipedia.org/wiki/Fumio_Tajima

    Fumio Tajima was born in Ōkawa, in Japan's Fukuoka prefecture, in 1951. [1] [2] He graduated from high school in 1970, completed his undergraduate degree at Kyushu University in 1976, and received a Master's degree from the same institution in 1978. [3]

  5. Infinite sites model - Wikipedia

    en.wikipedia.org/wiki/Infinite_sites_model

    The four gamete rule can be applied to the data to ensure that they do not violate the model assumption of no recombination. [ 4 ] The mutation rate ( θ {\displaystyle \theta } ) can be estimated as follows, where μ ∗ {\displaystyle \mu ^{*}} is the number of mutations found within a randomly selected DNA sequence (per generation), N e ...

  6. Allele frequency spectrum - Wikipedia

    en.wikipedia.org/wiki/Allele_frequency_spectrum

    The allele frequency spectrum can be written as the vector = (,,,,), where is the number of observed sites with derived allele frequency .In this example, the observed allele frequency spectrum is (,,,,), due to four instances of a single observed derived allele at a particular SNP loci, two instances of two derived alleles, and so on.

  7. Models of DNA evolution - Wikipedia

    en.wikipedia.org/wiki/Models_of_DNA_evolution

    By expressing models in terms of the instantaneous rates of change we can avoid estimating a large numbers of parameters for each branch on a phylogenetic tree (or each comparison if the analysis involves many pairwise sequence comparisons). The models described on this page describe the evolution of a single site within a set of sequences.

  8. Population genomics - Wikipedia

    en.wikipedia.org/wiki/Population_genomics

    Population genomics is the large-scale comparison of DNA sequences of populations. Population genomics is a neologism that is associated with population genetics.Population genomics studies genome-wide effects to improve our understanding of microevolution so that we may learn the phylogenetic history and demography of a population.

  9. Fay and Wu's H - Wikipedia

    en.wikipedia.org/wiki/Fay_and_Wu's_H

    Fay and Wu's H is a statistical test created by and named after two researchers Justin Fay and Chung-I Wu. [1] The purpose of the test is to distinguish between a DNA sequence evolving randomly ("neutrally") and one evolving under positive selection.