用多图证据融合提升癌症基因识别准确率
Soft-Evidence Fused Graph Neural Network for Cancer Driver Gene Identification across Multi-View Biological Graphs
- 各生物图作为独立证据源,决策层融合
- 新方法在3个数据集上超越现有最佳
- 适合做癌症基因发现的科研人员
识别癌症驱动基因(CDGs)对于理解癌症机制和开发靶向治疗至关重要。图神经网络(GNN)近期被用于捕捉生物互作网络中的模式以识别CDGs。然而,多数基于GNN的方法仅依赖单一蛋白质-蛋白质互作(PPI)网络,忽略了其他生物网络的互补信息。部分研究通过特征一致性约束对齐多网络特征以学习统一基因表示,但此类表示层面融合常假设网络间关系一致,可能忽略网络异质性并引入冲突信息。为此,我们提出软证据融合图神经网络(SEFGNN),一种在决策层实现跨多网络CDG识别的新框架。SEFGNN将每个生物网络视为独立证据源,利用德普斯特-谢弗理论(DST)进行不确定性感知融合。为缓解DST可能导致的过度自信问题,我们进一步引入软证据平滑(SES)模块,在保持判别性能的同时提升排序稳定性。在三个癌症数据集上的实验表明,SEFGNN持续优于当前最优基线,并展现出发现新CDGs的强大潜力。
原文摘要 · Abstract (English)
Identifying cancer driver genes (CDGs) is essential for understanding cancer mechanisms and developing targeted therapies. Graph neural networks (GNNs) have recently been employed to identify CDGs by capturing patterns in biological interaction networks. However, most GNN-based approaches rely on a single protein-protein interaction (PPI) network, ignoring complementary information from other biological networks. Some studies integrate multiple networks by aligning features with consistency constraints to learn unified gene representations for CDG identification. However, such representation-level fusion often assumes congruent gene relationships across networks, which may overlook network heterogeneity and introduce conflicting information. To address this, we propose Soft-Evidence Fusion Graph Neural Network (SEFGNN), a novel framework for CDG identification across multiple networks at the decision level. Instead of enforcing feature-level consistency, SEFGNN treats each biological network as an independent evidence source and performs uncertainty-aware fusion at the decision level using Dempster-Shafer Theory (DST). To alleviate the risk of overconfidence from DST, we further introduce a Soft Evidence Smoothing (SES) module that improves ranking stability while preserving discriminative performance. Experiments on three cancer datasets show that SEFGNN consistently outperforms state-of-the-art baselines and exhibits strong potential in discovering novel CDGs.
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