The Metabolomics Core Laboratory, Center of Genomic Medicine, National Taiwan University, No. 1 Sec. 4, Roosevelt Road, Taipei, Taiwan, 106.
J Mass Spectrom. 2013 Feb;48(2):234-42. doi: 10.1002/jms.3154.
Liquid Chromatography-Time of Flight Mass Spectrometry has become an important technique for toxicological screening and metabolomics. We describe TIPick a novel algorithm that accurately and sensitively detects target compounds in biological samples. TIPick comprises two main steps: background subtraction and peak picking. By subtracting a blank chromatogram, TIPick eliminates chemical signals of blank injections and reduces false positive results. TIPick detects peaks by calculating the S(CC(INI)) values of extracted ion chromatograms (EICs) without considering peak shapes, and it is able to detect tailing and fronting peaks. TIPick also uses duplicate injections to enhance the signals of the peaks and thus improve the peak detection power. Commonly seen split peaks caused by either saturation of the mass spectrometer detector or a mathematical background subtraction algorithm can be resolved by adjusting the mass error tolerance of the EICs and by comparing the EICs before and after background subtraction. The performance of TIPick was tested in a data set containing 297 standard mixtures; the recall, precision and F-score were 0.99, 0.97 and 0.98, respectively. TIPick was successfully used to construct and analyze the NTU MetaCore metabolomics chemical standards library, and it was applied for toxicological screening and metabolomics studies.
液相色谱 - 飞行时间质谱已成为毒理学筛选和代谢组学的重要技术。我们描述了一种新颖的算法 TIPick,该算法可以准确且敏感地检测生物样品中的目标化合物。TIPick 包括两个主要步骤:背景减除和峰提取。通过减去空白色谱图,TIPick 消除了空白进样的化学信号,减少了假阳性结果。TIPick 通过计算提取离子色谱图(EIC)的 S(CC(INI)) 值来检测峰,而不考虑峰形,并且能够检测到拖尾和前沿峰。TIPick 还使用重复进样来增强峰的信号,从而提高峰检测能力。通常由于质谱仪检测器的饱和或数学背景减除算法引起的分裂峰,可以通过调整 EIC 的质量误差容限并比较背景减除前后的 EIC 来解决。TIPick 的性能在包含 297 个标准混合物的数据集进行了测试;召回率、精度和 F 分数分别为 0.99、0.97 和 0.98。TIPick 成功用于构建和分析 NTU MetaCore 代谢组学化学标准库,并应用于毒理学筛选和代谢组学研究。