arXiv:2410.13178cs.LGcs.AI2024-10ICLR被引 2

GeSubNet通过融合基因网络与患者数据,精准构建疾病亚型特异的基因互作图谱。

GeSubNet: Gene Interaction Inference for Disease Subtype Network Generation

  • 分步学习:从表达谱聚类亚型,用GNN捕获先验互作,再联合优化生成亚型特异性网络。
  • 在4个癌症数据集上,图评估指标平均提升20%以上,最高达56.6%。
  • 可识别83%概率影响患者分布的亚型特异基因,适合精准医疗研究者使用。

从知识库中提取基因功能网络面临疾病网络与亚型特异性变异不匹配的挑战。现有统计和深度学习方法难以有效整合数据库中的基因互作知识或显式学习亚型特异性互作。为解决此问题,我们提出GeSubNet,一种能预测基因互作并区分不同疾病亚型的统一表征学习框架。该框架包含三个模块:首先,深度生成模型从患者基因表达谱中学习不同疾病亚型;其次,图神经网络捕获来自知识库的先验基因网络表征,确保物理互作准确性;最后,通过结合推断损失与患者分离损失,利用图生成能力融合双重视觉,精炼学习到的表征。GeSubNet在四个癌症数据集上,四种图评估指标的平均提升分别为30.6%、21.0%、20.1%和56.6%。此外,我们进行生物模拟实验,评估超过11,000个候选基因中选定基因对亚型或患者分布的影响。结果表明,生成的网络有83%的可能性识别出影响患者分布转移的亚型特异基因。

原文摘要 · Abstract (English)

Retrieving gene functional networks from knowledge databases presents a challenge due to the mismatch between disease networks and subtype-specific variations. Current solutions, including statistical and deep learning methods, often fail to effectively integrate gene interaction knowledge from databases or explicitly learn subtype-specific interactions. To address this mismatch, we propose GeSubNet, which learns a unified representation capable of predicting gene interactions while distinguishing between different disease subtypes. Graphs generated by such representations can be considered subtype-specific networks. GeSubNet is a multi-step representation learning framework with three modules: First, a deep generative model learns distinct disease subtypes from patient gene expression profiles. Second, a graph neural network captures representations of prior gene networks from knowledge databases, ensuring accurate physical gene interactions. Finally, we integrate these two representations using an inference loss that leverages graph generation capabilities, conditioned on the patient separation loss, to refine subtype-specific information in the learned representation. GeSubNet consistently outperforms traditional methods, with average improvements of 30.6%, 21.0%, 20.1%, and 56.6% across four graph evaluation metrics, averaged over four cancer datasets. Particularly, we conduct a biological simulation experiment to assess how the behavior of selected genes from over 11,000 candidates affects subtypes or patient distributions. The results show that the generated network has the potential to identify subtype-specific genes with an 83% likelihood of impacting patient distribution shifts.

基因网络疾病亚型图神经网络精准医疗

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