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Mining for Peaks in LC-HRMS Datasets Using Finnee – A Case Study with Exhaled Breath Condensates from Healthy, Asthmatic, and COPD Patients

机译:使用Finnee挖掘LC-HRMS数据集中的峰 - 以健康,哮喘和COPD患者呼出呼吸凝聚物的案例研究

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摘要

Separation techniques hyphenated to high-resolution mass spectrometry are essential in untargeted metabolomic analyses. Due to the complexity and size of the resulting data, analysts rely on computer-assisted tools to mine for features that may represent a chromatographic signal. However, this step remains problematic, and a high number of false positives are often obtained. This work reports a novel approach where each step is carefully controlled to decrease the likelihood of errors. Datasets are first corrected for baseline drift and background noise before the MS scans are converted from profile to centroid. A new alignment strategy that includes purity control is introduced, and features are quantified using the original data with scans recorded as profile, not the extracted features. All the algorithms used in this work are part of the Finnee Matlab toolbox that is freely available. The approach was validated using metabolites in exhaled breath condensates to differentiate individuals diagnosed with asthma from patients with chronic obstructive pulmonary disease. With this new pipeline, twice as many markers were found with Finnee in comparison to XCMS-online, and nearly 50% more than with MS-Dial, two of the most popular freeware for untargeted metabolomics analysis.
机译:连字符为高分辨率质谱法的分离技术对于未确定的代谢分析是必不可少的。由于所得数据的复杂性和大小,分析师依赖于可以代表色谱信号的计算机辅助工具来挖掘。然而,该步骤仍然存在问题,通常获得大量的误报。这项工作报告了一种新的方法,其中仔细控制每个步骤以降低错误的可能性。在MS扫描从配置文件转换为质心转换之前,首先纠正基线漂移和背景噪声的数据集。引入了包括纯度控制的新的对齐策略,并且使用扫描记录为简档的原始数据量化功能,而不是提取的功能。这项工作中使用的所有算法都是Finnee Matlab工具箱的一部分,可自由使用。使用呼出的呼吸凝聚物中的代谢物验证了该方法,以区分患有慢性阻塞性肺病患者患有哮喘的个体。使用这一新的管道,与XCMS-Online相比,使用Fin2的标记的两倍,并且比MS-Dial的近50%,两个最流行的自由软件用于未确定的代谢组科分析。

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