Fusion of Quality Evaluation Metrics and Convolutional Neural Network Representations for ROI Filtering in LC–MS

人工智能 卷积神经网络 计算机科学 假阳性悖论 假阳性率 模式识别(心理学) 感兴趣区域 机器学习 数据挖掘
作者
Hailiang Zhang,Zhenbo Xu,Xiaqiong Fan,Yue Wang,Qiong Yang,Jinyu Sun,Ming Wen,Xiao Kang,Zhimin Zhang,Hongmei Lü
出处
期刊:Analytical Chemistry [American Chemical Society]
被引量:6
标识
DOI:10.1021/acs.analchem.2c01398
摘要

Region of interest (ROI) extraction is a fundamental step in analyzing metabolomic datasets acquired by liquid chromatography–mass spectrometry (LC–MS). However, noises and backgrounds in LC–MS data often affect the quality of extracted ROIs. Therefore, developing effective ROI evaluation algorithms is necessary to eliminate false positives meanwhile keep the false-negative rate as low as possible. In this study, a deep fused filter of ROIs (dffROI) was proposed to improve the accuracy of ROI extraction by combining the handcrafted evaluation metrics with convolutional neural network (CNN)-learned representations. To evaluate the performance of dffROI, dffROI was compared with peakonly (CNN-learned representation) and five handcrafted metrics on three LC–MS datasets and a gas chromatography–mass spectrometry (GC–MS) dataset. Results show that dffROI can achieve higher accuracy, better true-positive rate, and lower false-positive rate. Its accuracy, true-positive rate, and false-positive rate are 0.9841, 0.9869, and 0.0186 on the test set, respectively. The classification error rate of dffROI (1.59%) is significantly reduced compared with peakonly (2.73%). The model-agnostic feature importance demonstrates the necessity of fusing handcrafted evaluation metrics with the convolutional neural network representations. dffROI is an automatic, robust, and universal method for ROI filtering by virtue of information fusion and end-to-end learning. It is implemented in Python programming language and open-sourced at https://github.com/zhanghailiangcsu/dffROI under BSD License. Furthermore, it has been integrated into the KPIC2 framework previously proposed by our group to facilitate real metabolomic LC–MS dataset analysis.

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