Prochlorococcus have low global mutation rate and small effective population size

Author(s):  
Zhuoyu Chen ◽  
Xiaojun Wang ◽  
Yu Song ◽  
Qinglu Zeng ◽  
Yao Zhang ◽  
...  
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.


2009 ◽  
Vol 11 (2) ◽  
pp. 539-546 ◽  
Author(s):  
Sanne Boessenkool ◽  
Bastiaan Star ◽  
Philip J. Seddon ◽  
Jonathan M. Waters

Genetics ◽  
1997 ◽  
Vol 146 (4) ◽  
pp. 1489-1499 ◽  
Author(s):  
Yun-Xin Fu

A coalescent theory for a sample of DNA sequences from a partially selfing diploid population and an algorithm for simulating such samples are developed in this article. Approximate formulas are given for the expectation and the variance of the number of segregating sites in a sample of k sequences from n individuals. Several new estimators of the important parameters θ = 4Nμ and the selfing rate s, where N and μ are, respectively, the effective population size and the mutation rate per sequence per generation, are proposed and their sampling properties are studied.


Genetics ◽  
1977 ◽  
Vol 85 (2) ◽  
pp. 331-337
Author(s):  
Wen-Hsiung Li

ABSTRACT Watterson's (1975) formula for the steady-state distribution of the number of nucleotide differences between two randomly chosen cistrons in a finite population has been extended to transient states. The rate for the mean of this distribution to approach its equilibrium value is 1/2 N and independent of mutation rate, but that for the variance is dependent on mutation rate, where N denotes the effective population size. Numerical computations show that if the heterozygosity (i.e., the probability that two cistrons are different) is low, say of the order of 0.1 or less, the probability that two cistrons differ at two or more nucleotide sites is less than 10 percent of the heterozygosity, whereas this probability may be as high as 50 percent of the heterozygosity if the heterozygosity is 0.5. A simple estimate for the mean number (d) of site differences between cistrons is d = h/(1 - h) where h is the heterozygosity. At equilibrium, the probability that two cistrons differ by more than one site is equal to h  2, the square of heterozygosity.


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