从SNP等位基因频率估计协方差结构

IF 0.9 4区 数学 Q3 Mathematics
J. van Waaij, Zilong Li, C. Wiuf
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引用次数: 1

摘要

摘要:本文提出了两个新的统计量V´$\hat{V}$和S´$\hat{S}$,用于从SNP频率数据中分离相关种群的种群历史。如果种群与树相关,我们通过理论手段和模拟表明,与标准统计(如观察到的f2统计矩阵(种群对之间的距离))相比,新的统计能够正确地识别树的根。统计量V´$\hat{V}$是通过对所有snp进行平均得到的(类似于标准统计量)。它的期望是观察到的总体SNP频率的真实协方差矩阵,由具有相同条目的矩阵抵消。相比之下,统计S´$\hat{S}$被放在贝叶斯上下文中,并通过对SNP进行平均来获得,这样每个SNP只使用一次。因此,它利用了snp对的联合分布。此外,我们还提供了一些关于新旧统计及其相互关系的新颖数学结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimation of the covariance structure from SNP allele frequencies
Abstract We propose two new statistics, V ̂ $\hat{V}$ and S ̂ $\hat{S}$ , to disentangle the population history of related populations from SNP frequency data. If the populations are related by a tree, we show by theoretical means as well as by simulation that the new statistics are able to identify the root of a tree correctly, in contrast to standard statistics, such as the observed matrix of F 2-statistics (distances between pairs of populations). The statistic V ̂ $\hat{V}$ is obtained by averaging over all SNPs (similar to standard statistics). Its expectation is the true covariance matrix of the observed population SNP frequencies, offset by a matrix with identical entries. In contrast, the statistic S ̂ $\hat{S}$ is put in a Bayesian context and is obtained by averaging over pairs of SNPs, such that each SNP is only used once. It thus makes use of the joint distribution of pairs of SNPs. In addition, we provide a number of novel mathematical results about old and new statistics, and their mutual relationship.
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来源期刊
CiteScore
1.20
自引率
11.10%
发文量
8
审稿时长
6-12 weeks
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
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