可解释性
人工智能
可视化
计算机科学
人工神经网络
机器学习
癌细胞系
虚拟筛选
药物反应
数量结构-活动关系
传感器融合
特征(语言学)
融合
图形
模式识别(心理学)
药品
药物发现
变压器
药物靶点
信息融合
分子描述符
数据可视化
随机森林
计算模型
回归
数据挖掘
推车
作者
Zhihan Liu,Kairui Lyu,Ya Li,Xinghui Sun,Xin Gao,Bin Yu
标识
DOI:10.1021/acs.jmedchem.5c03438
摘要
Cancer drug response prediction is crucial for precision medicine, as it can improve treatment outcomes and reduce medical costs. However, existing models often ignore the geometric features of drug molecules and their interactions with cancer cells. To address this, this study proposes a multiomics fusion model named MTEGDRP. The model uses a transformer to extract high-level features from drug and cell data, as well as their interactions, while an equivariant graph neural network captures the spatial structure of drugs. In regression tasks, MTEGDRP performs better than current state-of-the-art methods. Ablation studies show that multiomics integration and molecular spatial information are effective. Visualization of the feature weights provides interpretability for the model. With its excellent prediction performance, MTEGDRP shows great potential as a useful tool for guiding anticancer drug design in precision medicine.
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