scholarly journals Variance and limiting distribution of coalescence times in a diploid model of a consanguineous population

Author(s):  
Alissa L. Severson ◽  
Shai Carmi ◽  
Noah A. Rosenberg
2020 ◽  
Author(s):  
Alissa L. Severson ◽  
Shai Carmi ◽  
Noah A. Rosenberg

AbstractRecent modeling studies interested in runs of homozygosity (ROH) and identity by descent (IBD) have sought to connect these properties of genomic sharing to pairwise coalescence times. Here, we examine a variety of features of pairwise coalescence times in models that consider consanguinity. In particular, we extend a recent diploid analysis of mean coalescence times for lineage pairs within and between individuals in a consanguineous population to derive the variance of coalescence times, studying its dependence on the frequency of consanguinity and the kinship coefficient of consanguineous relationships. We also introduce a separation-of-time-scales approach that treats consanguinity models analogously to mathematically similar phenomena such as partial selfing, using this approach to obtain coalescence-time distributions. This approach shows that the consanguinity model behaves similarly to a standard coalescent, scaling population size by a factor 1 − 3c, where c represents the kinship coefficient of a randomly chosen mating pair. It provides the explanation for an earlier result describing mean coalescence time in the consanguinity model in terms of c. The results extend the potential to make predictions about ROH and IBD in relation to demographic parameters of diploid populations.


2021 ◽  
Vol 73 (1) ◽  
pp. 62-67
Author(s):  
Ibrahim A. Ahmad ◽  
A. R. Mugdadi

For a sequence of independent, identically distributed random variable (iid rv's) [Formula: see text] and a sequence of integer-valued random variables [Formula: see text], define the random quantiles as [Formula: see text], where [Formula: see text] denote the largest integer less than or equal to [Formula: see text], and [Formula: see text] the [Formula: see text]th order statistic in a sample [Formula: see text] and [Formula: see text]. In this note, the limiting distribution and its exact order approximation are obtained for [Formula: see text]. The limiting distribution result we obtain extends the work of several including Wretman[Formula: see text]. The exact order of normal approximation generalizes the fixed sample size results of Reiss[Formula: see text]. AMS 2000 subject classification: 60F12; 60F05; 62G30.


Genetics ◽  
2002 ◽  
Vol 162 (2) ◽  
pp. 987-991 ◽  
Author(s):  
Gilean A T McVean

Abstract The degree of association between alleles at different loci, or linkage disequilibrium, is widely used to infer details of evolutionary processes. Here I explore how associations between alleles relate to properties of the underlying genealogy of sequences. Under the neutral, infinite-sites assumption I show that there is a direct correspondence between the covariance in coalescence times at different parts of the genome and the degree of linkage disequilibrium. These covariances can be calculated exactly under the standard neutral model and by Monte Carlo simulation under different demographic models. I show that the effects of population growth, population bottlenecks, and population structure on linkage disequilibrium can be described through their effects on the covariance in coalescence times.


Genetics ◽  
1998 ◽  
Vol 150 (3) ◽  
pp. 1187-1198 ◽  
Author(s):  
Mikkel H Schierup ◽  
Xavier Vekemans ◽  
Freddy B Christiansen

Abstract Expectations for the time scale and structure of allelic genealogies in finite populations are formed under three models of sporophytic self-incompatibility. The models differ in the dominance interactions among the alleles that determine the self-incompatibility phenotype: In the SSIcod model, alleles act codominantly in both pollen and style, in the SSIdom model, alleles form a dominance hierarchy, and in SSIdomcod, alleles are codominant in the style and show a dominance hierarchy in the pollen. Coalescence times of alleles rarely differ more than threefold from those under gametophytic self-incompatibility, and transspecific polymorphism is therefore expected to be equally common. The previously reported directional turnover process of alleles in the SSIdomcod model results in coalescence times lower and substitution rates higher than those in the other models. The SSIdom model assumes strong asymmetries in allelic action, and the most recessive extant allele is likely to be the most recent common ancestor. Despite these asymmetries, the expected shape of the allele genealogies does not deviate markedly from the shape of a neutral gene genealogy. The application of the results to sequence surveys of alleles, including interspecific comparisons, is discussed.


Genetics ◽  
1998 ◽  
Vol 150 (1) ◽  
pp. 449-458 ◽  
Author(s):  
Patrick C Phillips ◽  
Norman A Johnson

Abstract Synthetic lethals are variants at different loci that have little or no effect on viability singly but cause lethality in combination. The importance of synthetic lethals and, more generally, of synthetic deleterious loci (SDL) has been controversial. Here, we derive the expected frequencies for SDL under a mutation-selection balance for the complete haploid model and selected cases of the diploid model. We have also obtained simple approximations that demonstrate good fit to exact solutions based on numerical iterations. In the haploid case, equilibrium frequencies of carrier haplotypes (individuals with only a single mutation) are comparable to analogous single-locus results, after allowing for the effects of linkage. Frequencies in the diploid case, however, are much higher and more comparable to the square root of the single-locus results. In particular, when selection operates only on the double-mutant homozygote and linkage is not too tight, the expected frequency of the carriers is approximately the quartic root of the ratio between the mutation rate and the selection coefficient of the synthetics. For a reasonably wide set of models, the frequencies of carriers can be on the order of a few percent. The equilibrium frequencies of these deleterious alleles can be relatively high because, with SDL, both dominance and epistasis act to shield carriers from exposure to selection. We also discuss the possible role of SDL in maintaining genetic variation and in hybrid breakdown.


1993 ◽  
Vol 30 (02) ◽  
pp. 438-445
Author(s):  
R. M. Phatarfod

There are a number of cases in the theories of queues and dams where the limiting distribution of the pertinent processes is geometric with a modified initial term — herein called zero-modified geometric (ZMG). The paper gives a unified treatment of the various cases considered hitherto and some others by using a duality relation between random walks with impenetrable and with absorbing barriers, and deriving the probabilities of absorption by using Waldian identities. Thus the method enables us to distinguish between those cases where the limiting distribution would be ZMG and those where it would not.


1978 ◽  
Vol 15 (3) ◽  
pp. 645-649 ◽  
Author(s):  
Svante Janson

This paper gives an elementary proof that, under some general assumptions, the number of parts a convex set in Rd is divided into by a set of independent identically distributed hyperplanes is asymptotically normally distributed. An example is given where the distribution of hyperplanes is ‘too singular' to satisfy the assumptions, and where a different limiting distribution appears.


1996 ◽  
Vol 28 (2) ◽  
pp. 331-331
Author(s):  
Richard Cowan ◽  
Simone Chen

Consider a connected planar graph. A bounded face is said to be of type k, or is called a k-face, if the boundary of that face contains k edges. Under various natural rules for randomly dividing bounded faces by the addition of new edges, we investigate the limiting distribution of face type as the number of divisions increases.


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