人工神经网络
人工智能
计算机科学
机器学习
多层感知器
贝叶斯概率
适用范围
贝叶斯网络
随机森林
化学信息学
不确定度量化
贝叶斯推理
朴素贝叶斯分类器
概率逻辑
贝叶斯定理
推论
支持向量机
模式识别(心理学)
试验装置
数据挖掘
高斯过程
预处理器
超参数
预测建模
特征(语言学)
偏最小二乘回归
交叉验证
统计模型
过度拟合
Probit模型
逻辑回归
作者
Karla Mosquera Jami,Lenin Ramírez-Cando
标识
DOI:10.1093/toxsci/kfag147
摘要
Nanoparticle cytotoxicity prediction remains challenging due to the complex interplay of physicochemical properties and experimental conditions, compounded by the critical need for uncertainty quantification in safety assessments. Here, we present a hybrid computational framework integrating Quantitative Structure-Activity Relationship (QSAR) feature engineering with Bayesian Neural Networks (BNNs) to predict metallic nanoparticle toxicity while explicitly quantifying predictive uncertainty. Using a curated dataset of 1,363 experimental records (25 nanoparticle formulations) from multiple in vitro studies, with every model evaluated on formulations unseen during training, we implemented a three-stage pipeline: (i) domain-guided preprocessing with multicollinearity assessment, (ii) benchmarking of deterministic classifiers (Random Forest, SVM, Multi-Layer Perceptron and three simpler models), and (iii) variational Bayesian inference for probabilistic classification. In repeated formulation-grouped cross-validation Random Forest discriminated best (ROC-AUC = 0.974), followed by logistic regression (0.967), which was better calibrated on held-out formulations (ECE 0.046 versus 0.130). The BNN discriminated well (ROC-AUC = 0.979) but underestimated toxicity at the 0.5 threshold (recall 0.520), while providing individual prediction uncertainty estimates from the variational posterior. Predictive uncertainty identified most misclassified predictions (AUROC = 0.92) but did not rise for samples outside the training descriptor space, which were detected by leverage. Dual-criterion applicability domain filtering (leverage and uncertainty thresholds) retained 44.2% of test samples (52 of the 125 toxic ones), achieving 0.942 recall and a 0.058 false negative rate, and flagged the remaining 55.8% for confirmatory testing. Impact statement: uncertainty-aware models evaluated on unseen formulations can separate nanoparticle cytotoxicity predictions usable for screening from those that require confirmatory testing.
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