The scientific study of short- and long-term changes in the size and age composition of populations and the processes driving these changes.

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Linkage disequilibrium with $n_l$ loci $n_a$ alleles

Linkage disequilibrium $\left(D\right)$ for two bi-allelic loci is defined as: $$D=X_{11}X_{22} - X_{12}X_{21}$$ , where $X_{11}$, $X_{12}$, $X_{21}$, X$_{22}$ are the frequencies of the haplotypes ...
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Effective population size and overlapping generations

From this book; If generations overlap, then the effective population size $N_e$ does not equal the population size $N$. I know mathematical formulations in order to find the effective population ...
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Selection on linked loci in a diploid population

Let’s consider two linked loci $A$ and $B$ that are both bi-allelic. In consequence, we have four different possible haplotypes $A_1B_1$, $A_1B_2$, $A_2B_1$, $A_2B_2$, which frequencies are $X_1$, ...
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Linkage disequilibrium, genetic drift and fitness variance

The very first two sentences of the abstract of this article is: "In finite populations subject to selection, genetic drift generates negative linkage disequilibrium, on average, even if selection ...
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90 views

Population genetics and the fitness probability distribution. Why is the arithmetic mean all we need?

When recording change in allele frequency in diploid, bi-allelic, infinite and panmixic population we usually use this kind of equation: $\delta_p = \frac{p * q *( p (w11 - w12) + q * (w12 - ...
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Why did the yeast rise?

Here are the notes I made for an experiment I was doing (I didn't put it here as it is too long) (please ignore the numbers at the end of the pdf file) The graph looks like this: As you see on ...
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47 views

Heterozygosity and overdominance

Consider $m$ loci with heterozygote advantage (overdominance) such that the fitness of the two homozygotes is $1-\frac{s}{2}$ and the fitness of the heterozygotes is $1+\frac{s}{2}$, where $s>0$. ...