Estimating effective population size from temporally spaced samples with a novel, efficient maximum-likelihood algorithm
The effective population size [Formula: see text] is a key parameter in population genetics and evolutionary biology, as it quantifies the expected distribution of changes in allele frequency due to genetic drift. Several methods of estimating [Formula: see text] have been described, the most direct...
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Veröffentlicht in: | Genetics (Austin) 2015-05, Vol.200 (1), p.285-293 |
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Sprache: | eng |
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Zusammenfassung: | The effective population size [Formula: see text] is a key parameter in population genetics and evolutionary biology, as it quantifies the expected distribution of changes in allele frequency due to genetic drift. Several methods of estimating [Formula: see text] have been described, the most direct of which uses allele frequencies measured at two or more time points. A new likelihood-based estimator [Formula: see text] for contemporary effective population size using temporal data is developed in this article. The existing likelihood methods are computationally intensive and unable to handle the case when the underlying [Formula: see text] is large. This article tries to work around this problem by using a hidden Markov algorithm and applying continuous approximations to allele frequencies and transition probabilities. Extensive simulations are run to evaluate the performance of the proposed estimator [Formula: see text], and the results show that it is more accurate and has lower variance than previous methods. The new estimator also reduces the computational time by at least 1000-fold and relaxes the upper bound of [Formula: see text] to several million, hence allowing the estimation of larger [Formula: see text]. Finally, we demonstrate how this algorithm can cope with nonconstant [Formula: see text] scenarios and be used as a likelihood-ratio test to test for the equality of [Formula: see text] throughout the sampling horizon. An R package "NB" is now available for download to implement the method described in this article. |
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ISSN: | 1943-2631 0016-6731 1943-2631 |
DOI: | 10.1534/genetics.115.174904 |