A stability property of the Ewens sampling formula

1983 ◽  
Vol 20 (3) ◽  
pp. 449-459 ◽  
Author(s):  
Stanley Sawyer

An error bound for convergence to the Ewens sampling formula is given where the population size or mutation rate may vary from generation to generation, or the population is not yet at equilibrium. An application is given to a model of Hartl and Campbell about selectively-equivalent subtypes within a class of deleterious alleles, and a theorem is proven showing that the size of the deleterious class stays within bounds sufficient to apply the first result. Generalizations are discussed.

1983 ◽  
Vol 20 (03) ◽  
pp. 449-459
Author(s):  
Stanley Sawyer

An error bound for convergence to the Ewens sampling formula is given where the population size or mutation rate may vary from generation to generation, or the population is not yet at equilibrium. An application is given to a model of Hartl and Campbell about selectively-equivalent subtypes within a class of deleterious alleles, and a theorem is proven showing that the size of the deleterious class stays within bounds sufficient to apply the first result. Generalizations are discussed.


1995 ◽  
Vol 32 (03) ◽  
pp. 609-622 ◽  
Author(s):  
Paul Joyce

Under the assumptions of the neutral infinite alleles model, K (the total number of alleles present in a sample) is sufficient for estimating θ (the mutation rate). This is a direct result of the Ewens sampling formula, which gives a consistent, asymptotically normal estimator for θ based on K. It is shown that the same estimator used to estimate θ under neutrality is consistent and asymptotically normal, even when the assumption of selective neutrality is violated.


1995 ◽  
Vol 32 (3) ◽  
pp. 609-622 ◽  
Author(s):  
Paul Joyce

Under the assumptions of the neutral infinite alleles model, K (the total number of alleles present in a sample) is sufficient for estimating θ (the mutation rate). This is a direct result of the Ewens sampling formula, which gives a consistent, asymptotically normal estimator for θ based on K. It is shown that the same estimator used to estimate θ under neutrality is consistent and asymptotically normal, even when the assumption of selective neutrality is violated.


Genetics ◽  
1994 ◽  
Vol 136 (4) ◽  
pp. 1475-1480 ◽  
Author(s):  
H A Orr ◽  
S P Otto

Abstract Explanations of the evolution of diploidy have focused on the advantages gained from masking deleterious alleles. Recent theory has shown, however, that masking does not always provide an advantage to diploidy and would never favor diploidy in predominantly asexual organisms. We explore a neglected alternative theory which posits that, by doubling the genome size, diploids double the rate at which favorable mutations arise. Consequently, the rate of adaptation in diploids is presumed to be faster than in haploids. The rate of adaptation, however, depends not only on the rate of appearance of new favorable mutations but also on the rate at which these mutations are incorporated (which depends on the population size and on the dominance of favorable mutations). We show that, in both asexuals and sexuals, doubling the mutation rate via diploidy often does not accelerate the rate of adaptation. Indeed, under many conditions, diploidy slows adaptation.


Genetics ◽  
1994 ◽  
Vol 136 (2) ◽  
pp. 685-692 ◽  
Author(s):  
Y X Fu

Abstract A new estimator of the essential parameter theta = 4Ne mu from DNA polymorphism data is developed under the neutral Wright-Fisher model without recombination and population subdivision, where Ne is the effective population size and mu is the mutation rate per locus per generation. The new estimator has a variance only slightly larger than the minimum variance of all possible unbiased estimators of the parameter and is substantially smaller than that of any existing estimator. The high efficiency of the new estimator is achieved by making full use of phylogenetic information in a sample of DNA sequences from a population. An example of estimating theta by the new method is presented using the mitochondrial sequences from an American Indian population.


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