Biosystems Data Analysis, Swammerdam Institute for Life Sciences, University of Amsterdam, The Netherlands.
Anal Chem. 2011 May 1;83(9):3267-74. doi: 10.1021/ac102374c. Epub 2011 Mar 10.
In the field of metabolomics, hundreds of metabolites are measured simultaneously by analytical platforms such as gas chromatography/mass spectrometry (GC/MS), liquid chromatography/mass spectrometry (LC/MS) and NMR to obtain their concentration levels in a reliable way. Analytical repeatability (intrabatch precision) is a common figure of merit for the measurement error of metabolites repeatedly measured in one batch on one platform. This measurement error, however, is not constant as its value may depend on the concentration level of the metabolite. Moreover, measurement errors may be correlated between metabolites. In this work, we introduce new figures of merit for comprehensive measurements that can detect these nonconstant correlated errors. Furthermore, for the metabolomics case we identified that these nonconstant correlated errors can result from sample instability between repeated analyses, instrumental noise generated by the analytical platform, or bias that results from data pretreatment.
在代谢组学领域,通过气相色谱/质谱(GC/MS)、液相色谱/质谱(LC/MS)和 NMR 等分析平台可以同时测量数百种代谢物,以可靠的方式获得它们的浓度水平。分析重复性(批内精密度)是在同一平台上对一批中重复测量的代谢物的测量误差的常用度量标准。然而,这种测量误差并不是恒定的,因为它的值可能取决于代谢物的浓度水平。此外,代谢物之间的测量误差可能是相关的。在这项工作中,我们引入了新的综合测量的度量标准,可以检测这些非恒定相关的误差。此外,对于代谢组学案例,我们发现这些非恒定相关的误差可能是由于重复分析之间的样本不稳定、分析平台产生的仪器噪声或数据预处理产生的偏差所致。