首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Detection of batch effects in liquid chromatography-mass spectrometry metabolomic data using guided principal component analysis
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Detection of batch effects in liquid chromatography-mass spectrometry metabolomic data using guided principal component analysis

机译:引导主成分分析法检测液相色谱-质谱代谢组学数据中的批次效应

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摘要

Metabolomics based on liquid chromatography-mass spectrometry (LC-MS) is a powerful tool for studying dynamic responses of biological systems to different physiological or pathological conditions. Differences in the instrumental response within and between batches introduce unwanted and uncontrolled data variation that should be removed to extract useful information. This work exploits a recently developed method for the identification of batch effects in high throughput genomic data based on the calculation of a δ statistic through principal component analysis (PCA) and guided PCA. Its applicability to LC-MS metabolomic data was tested on two real examples. The first example involved the repeated analysis of 42 plasma samples and 6 blanks in three independent batches, and the second data set involved the analysis of 101 plasma and 18 blank samples in a single batch with a total runtime of 50 h. The first and second data set were used to evaluate between and within-batch effects using the δ statistic, respectively. Results obtained showed the usefulness of using the δ statistic together with other approaches such as summary statistics of peak intensity distributions, PCA scores plots or the monitoring of IS peak intensities. to detect and identify instrumental instabilities in LC-MS.
机译:基于液相色谱-质谱(LC-MS)的代谢组学是研究生物系统对不同生理或病理条件的动态响应的强大工具。批次之间以及批次之间仪器响应的差异会引入不必要的和不受控制的数据变化,应将其删除以提取有用的信息。这项工作基于通过主成分分析(PCA)和指导的PCA计算δ统计量,利用一种最新开发的方法来识别高通量基因组数据中的批次效应。在两个真实的实例上测试了它对LC-MS代谢组学数据的适用性。第一个示例涉及三个独立批次中的42个血浆样品和6个空白样品的重复分析,第二个数据集涉及单个批次中101个血浆和18个空白样品的分析,总运行时间为50小时。第一和第二数据集分别用于使用δ统计量评估批间效应和批内效应。获得的结果表明,将δ统计量与其他方法(例如峰强度分布的摘要统计,PCA得分图或IS峰强度的监测)一起使用是有用的。以检测和识别LC-MS中的仪器不稳定性。

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