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首页> 外文期刊>Clinical proteomics. >A simpler method of preprocessing MALDI-TOF MS data for differential biomarker analysis: Stem cell and melanoma cancer studies
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A simpler method of preprocessing MALDI-TOF MS data for differential biomarker analysis: Stem cell and melanoma cancer studies

机译:预处理MALDI-TOF MS数据以进行差异生物标志物分析的更简单方法:干细胞和黑色素瘤癌症研究

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摘要

Introduction. Raw spectral data from matrix-assisted laser desorption/ionisation time-of-flight (MALDI-TOF) with MS profiling techniques usually contains complex information not readily providing biological insight into disease. The association of identified features within raw data to a known peptide is extremely difficult. Data preprocessing to remove uncertainty characteristics in the data is normally required before performing any further analysis. This study proposes an alternative yet simple solution to preprocess raw MALDI-TOF-MS data for identification of candidate marker ions. Two in-house MALDI-TOF-MS data sets from two different sample sources (melanoma serum and cord blood plasma) are used in our study. Method. Raw MS spectral profiles were preprocessed using the proposed approach to identify peak regions in the spectra. The preprocessed data was then analysed using bespoke machine learning algorithms for data reduction and ion selection. Using the selected ions, an ANN-based predictive model was constructed to examine the predictive power of these ions for classification. Results: Our model identified 10 candidate marker ions for both data sets. These ion panels achieved over 90% classification accuracy on blind validation data. Receiver operating characteristics analysis was performed and the area under the curve for melanoma and cord blood classifiers was 0.991 and 0.986, respectively. Conclusion: The results suggest that our data preprocessing technique removes unwanted characteristics of the raw data, while preserving the predictive components of the data. Ion identification analysis can be carried out using MALDI-TOF-MS data with the proposed data preprocessing technique coupled with bespoke algorithms for data reduction and ion selection.
机译:介绍。利用质谱分析技术从基质辅助的激光解吸/电离飞行时间(MALDI-TOF)获得的原始光谱数据通常包含复杂的信息,无法轻易提供对疾病的生物学见解。将原始数据中的已识别特征与已知肽关联非常困难。在执行任何进一步分析之前,通常需要对数据进行预处理以消除数据中的不确定性特征。这项研究提出了一种替代性但简单的解决方案,用于对原始MALDI-TOF-MS数据进行预处理,以识别候选标记离子。在我们的研究中,使用了来自两个不同样品来源(黑色素瘤血清和脐带血浆)的两个内部MALDI-TOF-MS数据集。方法。使用建议的方法对原始质谱图谱进行预处理,以识别质谱图中的峰区域。然后使用定制的机器学习算法对预处理的数据进行分析,以进行数据缩减和离子选择。使用选定的离子,构建了基于ANN的预测模型,以检查这些离子用于分类的预测能力。结果:我们的模型为两个数据集确定了10个候选标记离子。这些离子板在盲验证数据上达到了90%以上的分类精度。进行受试者工作特征分析,黑色素瘤和脐血分类器的曲线下面积分别为0.991和0.986。结论:结果表明,我们的数据预处理技术可以删除原始数据的有害特征,同时保留数据的预测成分。可以使用MALDI-TOF-MS数据,结合所提出的数据预处理技术和定制算法进行数据还原和离子选择,从而进行离子鉴定分析。

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