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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Classification of high-speed gas chromatography-mass spectrometry data by principal component analysis coupled with piecewise alignment and feature selection
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Classification of high-speed gas chromatography-mass spectrometry data by principal component analysis coupled with piecewise alignment and feature selection

机译:主成分分析结合分段比对和特征选择对高速气相色谱-质谱数据进行分类

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摘要

A useful methodology is introduced for the analysis of data obtained via gas chromatography with mass spectrometry (GC-MS) utilizing a complete mass spectrum at each retention time interval in which a mass spectrum was collected. Principal component analysis (PCA) with preprocessing by both piecewise retention time alignment and analysis of variance (ANOVA) feature selection is applied to all mass channels collected. The methodology involves concatenating all concurrently measured individual m/z chromatograms from m/z 20 to 120 for each GC-MS separation into a row vector. All of the sample row vectors are incorporated into a matrix where each row is a sample vector. This matrix is piecewise aligned and reduced by ANOVA feature selection. Application of the preprocessing steps (retention time alignment and feature selection) to all mass channels collected during the chromatographic separation allows considerably more selective chemical information to be incorporated in the PCA classification, and is the primary novelty of the report. This methodology is objective and requires no knowledge of the specific analytes of interest, as in selective ion monitoring (SIM), and does not restrict the mass spectral data used, as in both SIM and total ion current (TIC) methods. Significantly, the methodology allows for the classification of data with low resolution in the chromatographic dimension because of the added selectivity from the complete mass spectral dimension. This allows for the successful classification of data over significantly decreased chromatographic separation times, since high-speed separations can be employed. The methodology is demonstrated through the analysis of a set of four differing gasoline samples that serve as model complex samples. For comparison, the gasoline samples are analyzed by GC-MS over both 10-min and 10-s separation times. The successfully classified 10-min GC-MS TIC data served as the benchmark analysis to compare to the 10-s data. When only alignment and feature selection was applied to the 10-s gasoline separations using GC-MS TIC data, PCA failed. PCA was successful for 10-s gasoline separations when the methodology was applied with all the m/z information. With ANOVA feature selection, chromatographic regions with Fisher ratios greater than 1500 were retained in a new matrix and subjected to PCA yielding successful classification for the 10-s separations. (c) 2006 Elsevier B.V. All rights reserved.
机译:引入了一种有用的方法,用于分析通过质谱联用气相色谱(GC-MS)获得的数据,该方法在收集质谱的每个保留时间间隔使用完整质谱。通过分段保留时间对齐和方差分析(ANOVA)特征选择进行预处理的主成分分析(PCA)应用于所有收集的质量通道。该方法包括将每次GC-MS分离的所有同时测量的m / z色谱图(从m / z 20到120)串联到行向量中。所有样本行向量都合并到一个矩阵中,其中每一行都是一个样本向量。该矩阵分段对齐,并通过ANOVA特征选择进行缩小。将预处理步骤(保留时间对齐和特征选择)应用于色谱分离过程中收集的所有质量通道,可以将更具选择性的化学信息纳入PCA分类,这是该报告的主要新颖之处。这种方法是客观的,不需要像选择性离子监测(SIM)中那样了解感兴趣的特定分析物,也不会像SIM和总离子流(TIC)方法中那样限制使用的质谱数据。值得注意的是,由于从完整的质谱图中增加了选择性,因此该方法可以对色谱图中的低分辨率数据进行分类。由于可以采用高速分离,因此可以在大大减少的色谱分离时间上成功分类数据。通过分析一组四个不同的汽油样品作为模型复杂样品,证明了该方法。为了进行比较,在10分钟和10秒的分离时间内通过GC-MS分析了汽油样品。成功分类的10分钟GC-MS TIC数据用作基准分析,以与10s数据进行比较。当仅使用GC-MS TIC数据将对齐和特征选择应用于10秒钟汽油分离时,PCA失败。当该方法与所有m / z信息一起应用时,PCA成功地完成了10秒汽油分离。通过ANOVA特征选择,费舍尔比率大于1500的色谱区域将保留在新的基质中,并进行PCA处理,可成功分类10 s分离。 (c)2006 Elsevier B.V.保留所有权利。

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