The latent roots of certain Markov chains arising in genetics: A new approach, I. Haploid models

1974 ◽  
Vol 6 (2) ◽  
pp. 260-290 ◽  
Author(s):  
C. Cannings

Haploid models of genetic drift in populations of constant size are considered. Generalizations of the models of Moran and Wright have been developed by Karlin and McGregor (for multiple alleles and non-overlapping generations), by Chia and Watterson (for two alleles and overlapping or non-overlapping generations) and by Chia (for multiple alleles and overlapping or non-overlapping generations), using conditioned branching processes. A new approach is developed which contains the models mentioned above and provides simpler expressions for the latent roots. A greater dependence between the birth events and death events can be permitted, and non-independent mutations treated.


1974 ◽  
Vol 6 (02) ◽  
pp. 260-290 ◽  
Author(s):  
C. Cannings

Haploid models of genetic drift in populations of constant size are considered. Generalizations of the models of Moran and Wright have been developed by Karlin and McGregor (for multiple alleles and non-overlapping generations), by Chia and Watterson (for two alleles and overlapping or non-overlapping generations) and by Chia (for multiple alleles and overlapping or non-overlapping generations), using conditioned branching processes. A new approach is developed which contains the models mentioned above and provides simpler expressions for the latent roots. A greater dependence between the birth events and death events can be permitted, and non-independent mutations treated.



1975 ◽  
Vol 7 (02) ◽  
pp. 264-282 ◽  
Author(s):  
C. Cannings

The method developed for the treatment of the classical drift models of Wright and Moran, and their generalizations, in Cannings (1974) are extended to more complex haploid models. The possibility of subdivision of the population, as for migration models and age-structured models, is incorporated. Models with variable size or reproductive structure determined by another Markov chain are analysed.



1975 ◽  
Vol 7 (2) ◽  
pp. 264-282 ◽  
Author(s):  
C. Cannings

The method developed for the treatment of the classical drift models of Wright and Moran, and their generalizations, in Cannings (1974) are extended to more complex haploid models. The possibility of subdivision of the population, as for migration models and age-structured models, is incorporated. Models with variable size or reproductive structure determined by another Markov chain are analysed.



1991 ◽  
Vol 110 (3) ◽  
pp. 545-558 ◽  
Author(s):  
J. D. Biggins ◽  
N. H. Bingham

The occurrence of certain ‘near-constancy phenomena’ in some aspects of the theory of (simple) branching processes forms the background for the work below. The problem arises out of work by Karlin and McGregor [8, 9]. A detailed study of the theoretical and numerical aspects of the Karlin–McGregor near-constancy phenomenon was given by Dubuc[7], and considered further by Bingham[4]. We give a new approach which simplifies and generalizes the results of these authors. The primary motivation for doing this was the recent work of Barlow and Perkins [3], who observed near-constancy in a framework not immediately covered by the results then known.



1978 ◽  
Vol 1 (6) ◽  
pp. 341-343
Author(s):  
Wolfgang J. Bühler


1975 ◽  
Vol 25 (2) ◽  
pp. 89-94 ◽  
Author(s):  
Edward Pollak ◽  
Barry C. Arnold

SUMMARYThe distribution of visits to a particular gene frequency in a finite population of size N with non-overlapping generations is derived. It is shown, by using well-known results from the theory of finite Markov chains, that all such distributions are geometric, with parameters dependent only on the set of bij's, where bij is the mean number of visits to frequency j/2N, given initial frequency i/2N. The variance of such a distribution does not agree with the value suggested by the diffusion method. An improved approximation is derived.



1973 ◽  
Vol 10 (03) ◽  
pp. 659-665
Author(s):  
Donald C. Raffety

R-positivity theory for Markov chains is used to obtain results for random environment branching processes whose environment random variables are independent and identically distributed and whose environmental extinction probabilities are equal. For certain processes whose eventual extinction is almost sure, it is shown that the distribution of population size conditioned by non-extinction at time n tends to a left eigenvector of the transition matrix. Limiting values of other conditional probabilities are given in terms of this left eigenvector and it is shown that the probability of non-extinction at time n approaches zero geometrically as n approaches ∞. Analogous results are obtained for processes whose extinction is not almost sure.



1987 ◽  
Vol 1 (3) ◽  
pp. 251-264 ◽  
Author(s):  
Sheldon M. Ross

In this paper we propose a new approach for estimating the transition probabilities and mean occupation times of continuous-time Markov chains. Our approach is to approximate the probability of being in a state (or the mean time already spent in a state) at time t by the probability of being in that state (or the mean time already spent in that state) at a random time that is gamma distributed with mean t.



1973 ◽  
Vol 10 (3) ◽  
pp. 659-665 ◽  
Author(s):  
Donald C. Raffety

R-positivity theory for Markov chains is used to obtain results for random environment branching processes whose environment random variables are independent and identically distributed and whose environmental extinction probabilities are equal. For certain processes whose eventual extinction is almost sure, it is shown that the distribution of population size conditioned by non-extinction at time n tends to a left eigenvector of the transition matrix. Limiting values of other conditional probabilities are given in terms of this left eigenvector and it is shown that the probability of non-extinction at time n approaches zero geometrically as n approaches ∞. Analogous results are obtained for processes whose extinction is not almost sure.



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