Convergence time to the Ewens sampling formula in the infinite alleles Moran model

2009 ◽  
Vol 60 (2) ◽  
pp. 189-206 ◽  
Author(s):  
Joseph C. Watkins
1990 ◽  
Vol 22 (01) ◽  
pp. 1-24 ◽  
Author(s):  
S. N. Ethier

We discuss two formulations of the infinitely-many-neutral-alleles diffusion model that can be used to study the ages of alleles. The first one, which was introduced elsewhere, assumes values in the set of probability distributions on the set of alleles, and the ages of the alleles can be inferred from its sample paths. We illustrate this approach by proving a result of Watterson and Guess regarding the probability that the most frequent allele is oldest. The second diffusion model, which is new, assumes values in the set of probability distributions on the set of pairs (x, a), where x is an allele and a is its age. We illustrate this second approach by proving an extension of the Ewens sampling formula to age-ordered samples due to Donnelly and Tavaré.


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.


2010 ◽  
Vol 47 (03) ◽  
pp. 732-751 ◽  
Author(s):  
Sabin Lessard

Recurrence equations for the number of types and the frequency of each type in a random sample drawn from a finite population undergoing discrete, nonoverlapping generations and reproducing according to the Cannings exchangeable model are deduced under the assumption of a mutation scheme with infinitely many types. The case of overlapping generations in discrete time is also considered. The equations are developed for the Wright-Fisher model and the Moran model, and extended to the case of the limit coalescent with nonrecurrent mutation as the population size goes to ∞ and the mutation rate to 0. Computations of the total variation distance for the distribution of the number of types in the sample suggest that the exact Moran model provides a better approximation for the sampling formula under the exact Wright-Fisher model than the Ewens sampling formula in the limit of the Kingman coalescent with nonrecurrent mutation. On the other hand, this model seems to provide a good approximation for a Λ-coalescent with nonrecurrent mutation as long as the probability of multiple mergers and the mutation rate are small enough.


This paper is concerned with models for the genetic variation of a sample of gametes from a large population. The need for consistency between different sample sizes limits the mathematical possibilities to what are here called ‘partition structures Distinctive among them is the structure described by the Ewens sampling formula, which is shown to enjoy a characteristic property of non-interference between the different alleles. This characterization explains the robustness of the Ewens formula when neither selection nor recurrent mutation is significant, although different structures arise from selective and ‘charge-state’ models


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