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T. Maruyama (1970)
Analysis of population structure. I. One-dimensional stepping-stone models of finite length.Annals of human genetics, 34 2
T. Maruyama (1970)
Rate of decrease of genetic variability in a subdivided populationBiometrika, 57
T. Maruyama (1970)
Stepping stone models of finite lengthAdvances in Applied Probability, 2
T. Maruyama (1970)
On the rate of decrease of heterozygosity in circular stepping stone models of populations.Theoretical population biology, 1 1
Cedric Smith (1969)
Local fluctuations in gene frequenciesAnnals of Human Genetics, 32
R. Lewontin, J. Hubby (1966)
A molecular approach to the study of genic heterozygosity in natural populations. II. Amount of variation and degree of heterozygosity in natural populations of Drosophila pseudoobscura.Genetics, 54 2
M. Kimura, T. Maruyama (1971)
Pattern of neutral polymorphism in a geographically structured population.Genetical research, 18 2
M. Kimura, J. Crow (1964)
THE NUMBER OF ALLELES THAT CAN BE MAINTAINED IN A FINITE POPULATION.Genetics, 49
M. Kimura (1953)
'Stepping stone' model of population, 3
(1948)
Les mathhat iques de l’hdr4ditd
Harris (1966)
Enzyme polymorphisms in man.Proceedings of the Royal Society
H. Harris (1966)
C. Genetics of Man Enzyme polymorphisms in manProceedings of the Royal Society of London. Series B. Biological Sciences, 164
James Crow, Takeo Maruyama (1971)
The number of neutral alleles maintained in a finite, geographically structured population.Theoretical population biology, 2 4
T. Maruyama (1971)
Speed of Gene Substitution in a Geographically Structured PopulationThe American Naturalist, 105
A. Robertson (1964)
The effect of non-random mating within inbred lines on the rate of inbreedingGenetics Research, 5
N. Jacobson (1951)
Lectures In Abstract Algebra
Britain Analysis of population structure 11. Two-dimensional stepping stone models of finite length and other geographically structured populations* BY TAKE0 MARUYAMA National Institute of Genetics, Mishivnu, Japan 1. INTRODUCTION AND MODELS Many human populations as well as other animal and plant populations are divided into colonies (villages).These colonies are usually distributed geographically on a plane, and the size of a colony may be small in the sense that the random drift may cause appreciable variation in the gene frequency among colonies. Usually these colonies constituting a population are not completely separated but there are some exchanges among them, and the closer two colonies are geographically the more exchanges there are. Therefore genetical similarity between colonies is a function of their distance and, of course, of the migration rate. Strictly speaking real population structure may be too complicated to be handled mathematically. However, the stepping stone model of a population structure proposed by Kimura (1953) is a mathematically tractable approximation to real situations. The population consists of colonies, each located at a gridpoint of 2-dimensional integer lattice. All colonies have equal and finite size ( N ) which does not vary in time. We use (i,j)to denote the position
Annals of Human Genetics – Wiley
Published: Oct 1, 1971
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