用组学数据应用多个端点的比较测试。

IF 0.9 4区 数学 Q3 Mathematics
Marco Marozzi
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引用次数: 2

摘要

在生物医学研究中,基因组学、蛋白质组学和代谢组学等“组学”领域通常分析多个端点。针对低维数据设计的传统方法在分析高维数据时要么表现不佳,要么不适用,因为高维数据的维度通常与受试者的数量相似,甚至远远大于受试者的数量。数百(或数千)个端点之间复杂的生化相互作用反映为复杂的依赖关系。本文的目的是提出非常适合分析组学数据的测试,因为它们不需要正态性假设,对于小样本量,在端点之间存在复杂依赖关系的情况下,以及当端点数量远远大于受试者数量时,它们也很强大。证明了试验的无偏性和一致性,并对试验的规模和效力进行了数值评价。结果表明,基于非参数组合点间距离检验的方法是非常有效的。讨论了基因组学和代谢组学的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tests for comparison of multiple endpoints with application to omics data.

In biomedical research, multiple endpoints are commonly analyzed in "omics" fields like genomics, proteomics and metabolomics. Traditional methods designed for low-dimensional data either perform poorly or are not applicable when analyzing high-dimensional data whose dimension is generally similar to, or even much larger than, the number of subjects. The complex biochemical interplay between hundreds (or thousands) of endpoints is reflected by complex dependence relations. The aim of the paper is to propose tests that are very suitable for analyzing omics data because they do not require the normality assumption, are powerful also for small sample sizes, in the presence of complex dependence relations among endpoints, and when the number of endpoints is much larger than the number of subjects. Unbiasedness and consistency of the tests are proved and their size and power are assessed numerically. It is shown that the proposed approach based on the nonparametric combination of dependent interpoint distance tests is very effective. Applications to genomics and metabolomics are discussed.

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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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