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G(ST) and its relatives do not measure differentiation

机译:G(ST)及其亲属无法衡量差异

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G(ST) and its relatives are often interpreted as measures of differentiation between subpopulations, with values near zero supposedly indicating low differentiation. However, G(ST) necessarily approaches zero when gene diversity is high, even if subpopulations are completely differentiated, and it is not monotonic with increasing differentiation. Likewise, when diversity is equated with heterozygosity, standard similarity measures formed by taking the ratio of mean within-subpopulation diversity to total diversity necessarily approach unity when diversity is high, even if the subpopulations are completely dissimilar (no shared alleles). None of these measures can be interpreted as measures of differentiation or similarity. The derivations of these measures contain two subtle misconceptions which cause their paradoxical behaviours. Conclusions about population differentiation, gene flow, relatedness, and conservation priority will often be wrong when based on these fixation indices or similarity measures. These are not statistical issues; the problems persist even when true population frequencies are used in the calculations. Recent advances in the mathematics of diversity identify the misconceptions, and yield mathematically consistent descriptive measures of population structure which eliminate the paradoxes produced by standard measures. These measures can be directly related to the migration and mutation rates of the finite-island model.
机译:G(ST)及其近亲通常被解释为亚群之间差异的量度,据称接近零的值表示较低的差异。但是,即使亚群完全分化,当基因多样性很高时,G(ST)也必定接近零,并且随着分化的增加,它不是单调的。同样,当多样性等同于杂合性时,即使子群体完全不同(没有共享等位基因),当多样性高时,通过采用平均亚种群内多样性与总多样性之比形成的标准相似性度量也必须趋于统一。这些措施都不能解释为区分或相似性的措施。这些措施的推导包含两个细微的误解,这些误解导致了它们的悖论行为。当基于这些固定指标或相似性度量时,关于种群分化,基因流动,相关性和保护优先级的结论通常是错误的。这些不是统计问题;即使在计算中使用了真实的人口频率,问题仍然存在。多样性数学的最新进展发现了误解,并产生了数学上一致的人口结构描述性测度,从而消除了标准测度产生的悖论。这些措施可以直接与有限岛模型的迁移和突变率相关。

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