存在外部协变量的基于树的定量性状映射。

Pub Date : 2016-12-01 DOI:10.1515/sagmb-2015-0107
Katherine L Thompson, Catherine R Linnen, Laura Kubatko
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引用次数: 2

摘要

生物学和生物医学科学的中心目标是确定形态和行为特征变异的分子基础。在过去的十年中,测序技术的改进以及关联作图方法的积极发展使得将单核苷酸多态性(snp)与数量性状联系起来成为可能。然而,现有方法的一个主要限制是,它们往往无法考虑复杂的,但生物学上现实的情况。先前的研究表明,利用每个SNP内部的进化史来估计随机抽样个体之间的协方差结构可以提高关联映射方法的性能。在这里,我们提出了一种方法,可以用于分析各种数据类型,例如包括外部协变量的数据,同时考虑snp之间的进化史,提供比现有方法的优势。现有的方法要么在计算成本上这样做,要么不能完全模拟这些关系。考虑到SNPs之间的大范围关系,所提出的方法在计算上是可行的,并且被SNPs之间的进化史所告知。我们表明,在复杂数据集的分析中加入近似协方差结构可以提高定量性状映射的性能,并将所提出的方法应用于鹿鼠数据。
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Tree-based quantitative trait mapping in the presence of external covariates.

A central goal in biological and biomedical sciences is to identify the molecular basis of variation in morphological and behavioral traits. Over the last decade, improvements in sequencing technologies coupled with the active development of association mapping methods have made it possible to link single nucleotide polymorphisms (SNPs) and quantitative traits. However, a major limitation of existing methods is that they are often unable to consider complex, but biologically-realistic, scenarios. Previous work showed that association mapping method performance can be improved by using the evolutionary history within each SNP to estimate the covariance structure among randomly-sampled individuals. Here, we propose a method that can be used to analyze a variety of data types, such as data including external covariates, while considering the evolutionary history among SNPs, providing an advantage over existing methods. Existing methods either do so at a computational cost, or fail to model these relationships altogether. By considering the broad-scale relationships among SNPs, the proposed approach is both computationally-feasible and informed by the evolutionary history among SNPs. We show that incorporating an approximate covariance structure during analysis of complex data sets increases performance in quantitative trait mapping, and apply the proposed method to deer mice data.

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