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Novel probabilistic models of spatial genetic ancestry with applications to stratification correction in genome-wide association studies

机译:空间遗传学的新型概率模型及其在全基因组关联研究中的分层校正中的应用

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摘要

>Motivation: Genetic variation in human populations is influenced by geographic ancestry due to spatial locality in historical mating and migration patterns. Spatial population structure in genetic datasets has been traditionally analyzed using either model-free algorithms, such as principal components analysis (PCA) and multidimensional scaling, or using explicit spatial probabilistic models of allele frequency evolution. We develop a general probabilistic model and an associated inference algorithm that unify the model-based and data-driven approaches to visualizing and inferring population structure. Our spatial inference algorithm can also be effectively applied to the problem of population stratification in genome-wide association studies (GWAS), where hidden population structure can create fictitious associations when population ancestry is correlated with both the genotype and the trait. >Results: Our algorithm Geographic Ancestry Positioning (GAP) relates local genetic distances between samples to their spatial distances, and can be used for visually discerning population structure as well as accurately inferring the spatial origin of individuals on a two-dimensional continuum. On both simulated and several real datasets from diverse human populations, GAP exhibits substantially lower error in reconstructing spatial ancestry coordinates compared to PCA. We also develop an association test that uses the ancestry coordinates inferred by GAP to accurately account for ancestry-induced correlations in GWAS. Based on simulations and analysis of a dataset of 10 metabolic traits measured in a Northern Finland cohort, which is known to exhibit significant population structure, we find that our method has superior power to current approaches. >Availability and Implementation: Our software is available at . >Contacts: or >Supplementary information: are available at Bioinformatics online.
机译:>动机:由于历史交配和迁移方式的空间局限性,人类遗传变异受地理背景的影响。传统上,已经使用无模型算法(例如主成分分析(PCA)和多维缩放)或使用等位基因频率进化的显式空间概率模型来分析遗传数据集中的空间种群结构。我们开发了一个通用的概率模型和相关的推理算法,以统一基于模型和数据驱动的方法来可视化和推断总体结构。我们的空间推断算法也可以有效地应用于全基因组关联研究(GWAS)中的人口分层问题,其中,当人口谱系与基因型和性状相关时,隐藏的人口结构可以创建虚拟关联。 >结果:我们的算法“地理祖先定位”(GAP)将样本之间的局部遗传距离与它们的空间距离相关联,可用于视觉上辨别种群结构以及准确推断两个个体的空间起源维连续体。与PCA相比,在来自不同人群的模拟数据集和一些实际数据集上,GAP在重构空间祖先坐标时表现出明显较低的误差。我们还开发了一种关联测试,该测试使用GAP推断的祖先坐标来准确说明GWAS中由祖先引起的相关性。基于对在北部芬兰队列中测量的10个代谢性状的数据集的模拟和分析,已知该数据集显示出重要的种群结构,我们发现我们的方法比当前方法更具优势。 >可用性和实施​​:我们的软件可从访问。 >联系人:或>补充信息:可从生物信息学在线获得。

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