Inferring demographic and selective histories from population genomic data using a 2-step approach in species with coding-sparse genomes: an application to human data.

IF 2.2 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2025-04-17 DOI:10.1093/g3journal/jkaf019
Vivak Soni, Jeffrey D Jensen
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Abstract

The demographic history of a population, and the distribution of fitness effects (DFE) of newly arising mutations in functional genomic regions, are fundamental factors dictating both genetic variation and evolutionary trajectories. Although both demographic and DFE inference has been performed extensively in humans, these approaches have generally either been limited to simple demographic models involving a single population, or, where a complex population history has been inferred, without accounting for the potentially confounding effects of selection at linked sites. Taking advantage of the coding-sparse nature of the genome, we propose a 2-step approach in which coalescent simulations are first used to infer a complex multi-population demographic model, utilizing large non-functional regions that are likely free from the effects of background selection. We then use forward-in-time simulations to perform DFE inference in functional regions, conditional on the complex demography inferred and utilizing expected background selection effects in the estimation procedure. Throughout, recombination and mutation rate maps were used to account for the underlying empirical rate heterogeneity across the human genome. Importantly, within this framework it is possible to utilize and fit multiple aspects of the data, and this inference scheme represents a generalized approach for such large-scale inference in species with coding-sparse genomes.

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利用编码稀疏基因组物种的两步方法从种群基因组数据推断人口统计学和选择历史:在人类数据中的应用。
种群的人口历史和功能基因组区域新突变的适应度效应(DFE)分布是决定遗传变异和进化轨迹的基本因素。尽管人口统计学和DFE推断已经在人类中得到了广泛的应用,但这些方法通常要么局限于涉及单个种群的简单人口统计学模型,要么局限于推断出复杂的种群历史,而没有考虑到连锁位点选择的潜在混淆效应。利用基因组的编码稀疏特性,我们提出了一种两步方法,首先使用聚结模拟来推断复杂的多种群人口模型,利用可能不受背景选择影响的大型非功能区。然后,我们使用前向实时模拟在功能区进行DFE推断,条件是推断出复杂的人口统计数据,并在估计过程中利用预期的背景选择效应。在整个过程中,重组和突变率图被用来解释人类基因组中潜在的经验率异质性。重要的是,在这个框架内,可以利用和拟合数据的多个方面,并且该推理方案代表了在编码稀疏基因组的物种中进行这种大规模推理的通用方法。
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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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