A novel method to accurately calculate statistical significance of local similarity analysis for high-throughput time series.

IF 0.9 4区 数学 Q3 Mathematics
Fang Zhang, Ang Shan, Yihui Luan
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引用次数: 2

Abstract

In recent years, a large number of time series microbial community data has been produced in molecular biological studies, especially in metagenomics. Among the statistical methods for time series, local similarity analysis is used in a wide range of environments to capture potential local and time-shifted associations that cannot be distinguished by traditional correlation analysis. Initially, the permutation test is popularly applied to obtain the statistical significance of local similarity analysis. More recently, a theoretical method has also been developed to achieve this aim. However, all these methods require the assumption that the time series are independent and identically distributed. In this paper, we propose a new approach based on moving block bootstrap to approximate the statistical significance of local similarity scores for dependent time series. Simulations show that our method can control the type I error rate reasonably, while theoretical approximation and the permutation test perform less well. Finally, our method is applied to human and marine microbial community datasets, indicating that it can identify potential relationship among operational taxonomic units (OTUs) and significantly decrease the rate of false positives.

一种精确计算高通量时间序列局部相似度统计显著性的新方法。
近年来,分子生物学特别是宏基因组学研究中产生了大量的时间序列微生物群落数据。在时间序列的统计方法中,局部相似度分析用于广泛的环境中,以捕获传统相关分析无法区分的潜在局部关联和时移关联。最初,人们普遍采用排列检验来获得局部相似性分析的统计显著性。最近,也发展了一种理论方法来实现这一目标。然而,所有这些方法都要求假设时间序列是独立的和同分布的。在本文中,我们提出了一种新的基于移动块自举的方法来近似依赖时间序列的局部相似分数的统计显著性。仿真结果表明,该方法能较好地控制第一类错误率,而理论逼近和排列测试的效果较差。最后,将该方法应用于人类和海洋微生物群落数据集,结果表明该方法可以识别出操作分类单元(otu)之间的潜在关系,并显著降低了误报率。
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
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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