The Meaning and Measure of Concordance Factors in Phylogenomics.

IF 11 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Robert Lanfear, Matthew W Hahn
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引用次数: 0

Abstract

As phylogenomic datasets have grown in size, researchers have developed new ways to measure biological variation and to assess statistical support for specific branches. Larger datasets have more sites and loci and therefore less sampling variance. While we can more accurately measure the mean signal in these datasets, lower sampling variance is often reflected in uniformly high measures of branch support-such as the bootstrap and posterior probability-limiting their utility. Larger datasets have also revealed substantial biological variation in the topologies found across individual loci, such that the single species tree inferred by most phylogenetic methods represents a limited summary of the data for many purposes. In contrast to measures of statistical support, the degree of underlying topological variation among loci should be approximately constant regardless of the size of the dataset. "Concordance factors" (CFs) and similar statistics have therefore become increasingly important tools in phylogenetics. In this review, we explain why CFs should be thought of as descriptors of topological variation rather than as measures of statistical support, and argue that they provide important information about the predictive power of the species tree not contained in measures of support. We review a growing suite of statistics for measuring concordance, compare them in a common framework that reveals their interrelationships, and demonstrate how to calculate them using an example from birds. We also discuss how measures of topological variation might change in the future as we move beyond estimating a single "tree of life" toward estimating the myriad evolutionary histories underlying genomic variation.

系统发生组学中一致性因子的意义和测量方法。
随着系统发生组数据集规模的不断扩大,研究人员开发出了衡量生物变异和评估特定分支统计支持度的新方法。较大的数据集拥有更多的位点和位点,因此取样方差较小。虽然我们可以更准确地测量这些数据集中的平均信号,但较低的取样方差往往反映在较高的分支支持度量上,如自举法(bootstrap)和后验概率(posterior probability),从而限制了它们的效用。较大的数据集也揭示了单个位点拓扑结构的巨大生物差异,因此大多数系统发育方法推断出的单一物种树在很多情况下只能代表数据的有限总结。与统计支持度相比,无论数据集的大小如何,基因位点间基本拓扑结构的变化程度应大致恒定。因此,"一致性因子 "和类似的统计量已成为系统发生学中越来越重要的工具。在这篇综述中,我们解释了为什么应将协整因子视为拓扑变异的描述符而不是统计支持度量,并认为协整因子提供了支持度量中未包含的有关物种树预测能力的重要信息。我们回顾了越来越多的测量一致性的统计方法,在一个共同的框架内对它们进行了比较,揭示了它们之间的相互关系,并以鸟类为例演示了如何计算它们。我们还讨论了拓扑变异的测量方法在未来可能发生的变化,因为我们已经从估算单一的 "生命之树 "转向估算基因组变异背后的无数进化历史。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular biology and evolution
Molecular biology and evolution 生物-进化生物学
CiteScore
19.70
自引率
3.70%
发文量
257
审稿时长
1 months
期刊介绍: Molecular Biology and Evolution Journal Overview: Publishes research at the interface of molecular (including genomics) and evolutionary biology Considers manuscripts containing patterns, processes, and predictions at all levels of organization: population, taxonomic, functional, and phenotypic Interested in fundamental discoveries, new and improved methods, resources, technologies, and theories advancing evolutionary research Publishes balanced reviews of recent developments in genome evolution and forward-looking perspectives suggesting future directions in molecular evolution applications.
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