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定量代谢组学中的样本归一化方法。

Sample normalization methods in quantitative metabolomics.

作者信息

Wu Yiman, Li Liang

机构信息

Department of Chemistry, University of Alberta, Edmonton, AB, T6G2G2, Canada.

Department of Chemistry, University of Alberta, Edmonton, AB, T6G2G2, Canada.

出版信息

J Chromatogr A. 2016 Jan 22;1430:80-95. doi: 10.1016/j.chroma.2015.12.007. Epub 2015 Dec 10.

Abstract

To reveal metabolomic changes caused by a biological event in quantitative metabolomics, it is critical to use an analytical tool that can perform accurate and precise quantification to examine the true concentration differences of individual metabolites found in different samples. A number of steps are involved in metabolomic analysis including pre-analytical work (e.g., sample collection and storage), analytical work (e.g., sample analysis) and data analysis (e.g., feature extraction and quantification). Each one of them can influence the quantitative results significantly and thus should be performed with great care. Among them, the total sample amount or concentration of metabolites can be significantly different from one sample to another. Thus, it is critical to reduce or eliminate the effect of total sample amount variation on quantification of individual metabolites. In this review, we describe the importance of sample normalization in the analytical workflow with a focus on mass spectrometry (MS)-based platforms, discuss a number of methods recently reported in the literature and comment on their applicability in real world metabolomics applications. Sample normalization has been sometimes ignored in metabolomics, partially due to the lack of a convenient means of performing sample normalization. We show that several methods are now available and sample normalization should be performed in quantitative metabolomics where the analyzed samples have significant variations in total sample amounts.

摘要

在定量代谢组学中,为揭示生物事件引起的代谢组学变化,使用一种能够进行准确且精确量化的分析工具来检测不同样本中单个代谢物的真实浓度差异至关重要。代谢组学分析涉及多个步骤,包括分析前工作(如样本采集和存储)、分析工作(如样本分析)和数据分析(如特征提取和量化)。其中每一步都可能对定量结果产生重大影响,因此都应谨慎进行。在这些步骤中,不同样本之间代谢物的总样本量或浓度可能存在显著差异。因此,减少或消除总样本量变化对单个代谢物定量的影响至关重要。在本综述中,我们阐述了样本归一化在分析流程中的重要性,重点关注基于质谱(MS)的平台,讨论了文献中最近报道的一些方法,并对它们在实际代谢组学应用中的适用性进行了评论。样本归一化在代谢组学中有时会被忽视,部分原因是缺乏进行样本归一化的便捷方法。我们表明,现在有几种方法可用,并且在被分析样本的总样本量存在显著差异的定量代谢组学中应进行样本归一化。

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