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And you probably know that most population genetic things that we want to measure are transformations of allele frequency, like heterozygosity.
Most population genetic and phylogeographic investigations produce large, complex data sets.
In most population genetic models, the population size refers to the sum of all individuals at a particular time.
Thus, analysis with population genetic methods in this system may be more appropriate than in other model systems since most population genetic models assume these characteristics and are sensitive to even slight violations.
Second, most population genetic parameters are sensitive to sample size.
We conclude that any reduction in malaria transmission left most population genetic parameters unchanged.
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Recall that the Hardy-Weinberg law, the starting point for most population-genetic analysis, was derived under the assumption of random mating.
Yet the ascertainment of the samples differs from most population-genetic studies which collect individuals who live in the same local region as their ancestors.
To date, most population-genetic studies of marine protists have focussed on a relatively small number of ecologically or economically important species such as harmful algae, coccolithophores and diatoms [e.g. [9],[16],[17],[14],[15], [ 16], [17]].
We first use a coalescent framework to generate datasets assuming no or different levels of heterochrony and contrast most classical population genetic statistics.
Most recent population genetic studies have utilized non-coding nuclear markers such as microsatellites or nuclear length variants such as amplified fragment length polymorphisms [ 15- 17, 19].
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