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线粒体错配分析对突变过程不敏感。

Mitochondrial mismatch analysis is insensitive to the mutational process.

作者信息

Rogers A R, Fraley A E, Bamshad M J, Watkins W S, Jorde L B

机构信息

Department of Anthropology, University of Utah, Salt Lake City 84112, USA.

出版信息

Mol Biol Evol. 1996 Sep;13(7):895-902. doi: 10.1093/molbev/13.7.895.

Abstract

Mismatch distributions are histograms showing the pattern of nucleotide (or restriction) site differences between pairs of individuals in a sample. They can be used to test hypotheses about the history of population size and subdivision (if selective neutrality is assumed) or about selection (if a constant population size is assumed). Previous work has assumed that mutations never strike the same site twice, an assumption that is called the model of infinite sites. Fortunately, the results are surprisingly robust even when this assumption is violated. We show here that (1) confidence regions inferred using the infinite-sites model differ little from those inferred using a model of finite sites with uniform site-specific mutation rates, and (2) even when site-specific mutation rates follow a gamma distribution, confidence regions are little changed until the gamma shape parameter falls well below its plausible range, to roughly 0.01. In addition, we evaluate and reject the proposition that mismatch waves are produced by pooling data from several subdivisions of a structured population.

摘要

错配分布是一种直方图,展示了样本中个体对之间核苷酸(或限制性)位点差异的模式。它们可用于检验关于种群大小历史和细分情况的假设(如果假设为选择性中性),或关于选择的假设(如果假设种群大小恒定)。先前的研究假设突变不会两次击中同一位点,这一假设被称为无限位点模型。幸运的是,即使违背这一假设,结果仍出人意料地稳健。我们在此表明:(1)使用无限位点模型推断出的置信区间与使用具有均匀位点特异性突变率的有限位点模型推断出的置信区间差异不大;(2)即使位点特异性突变率遵循伽马分布,在伽马形状参数降至其合理范围以下很远,大致为0.01之前,置信区间变化很小。此外,我们评估并否定了错配波是由合并结构化种群的几个细分数据产生的这一观点。

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