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用于预测人类癌症中合成致死性的图上下文注意力网络。

Graph contextualized attention network for predicting synthetic lethality in human cancers.

作者信息

Long Yahui, Wu Min, Liu Yong, Zheng Jie, Kwoh Chee Keong, Luo Jiawei, Li Xiaoli

机构信息

College of Computer Science and Electronic Engineering, Hunan University, Changsha 410000, China.

School of Computer Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.

出版信息

Bioinformatics. 2021 Aug 25;37(16):2432-2440. doi: 10.1093/bioinformatics/btab110.

Abstract

MOTIVATION

Synthetic Lethality (SL) plays an increasingly critical role in the targeted anticancer therapeutics. In addition, identifying SL interactions can create opportunities to selectively kill cancer cells without harming normal cells. Given the high cost of wet-lab experiments, in silico prediction of SL interactions as an alternative can be a rapid and cost-effective way to guide the experimental screening of candidate SL pairs. Several matrix factorization-based methods have recently been proposed for human SL prediction. However, they are limited in capturing the dependencies of neighbors. In addition, it is also highly challenging to make accurate predictions for new genes without any known SL partners.

RESULTS

In this work, we propose a novel graph contextualized attention network named GCATSL to learn gene representations for SL prediction. First, we leverage different data sources to construct multiple feature graphs for genes, which serve as the feature inputs for our GCATSL method. Second, for each feature graph, we design node-level attention mechanism to effectively capture the importance of local and global neighbors and learn local and global representations for the nodes, respectively. We further exploit multi-layer perceptron (MLP) to aggregate the original features with the local and global representations and then derive the feature-specific representations. Third, to derive the final representations, we design feature-level attention to integrate feature-specific representations by taking the importance of different feature graphs into account. Extensive experimental results on three datasets under different settings demonstrated that our GCATSL model outperforms 14 state-of-the-art methods consistently. In addition, case studies further validated the effectiveness of our proposed model in identifying novel SL pairs.

AVAILABILITYAND IMPLEMENTATION

Python codes and dataset are freely available on GitHub (https://github.com/longyahui/GCATSL) and Zenodo (https://zenodo.org/record/4522679) under the MIT license.

SUPPLEMENTARY INFORMATION

Supplementary data are available at Bioinformatics online.

摘要

动机

合成致死(SL)在靶向抗癌治疗中发挥着越来越关键的作用。此外,识别SL相互作用可以创造机会选择性地杀死癌细胞而不损害正常细胞。鉴于湿实验室实验成本高昂,作为一种替代方法,通过计算机模拟预测SL相互作用可以是一种快速且经济高效的方式来指导候选SL对的实验筛选。最近已经提出了几种基于矩阵分解的方法用于人类SL预测。然而,它们在捕捉邻居的依赖性方面存在局限性。此外,对于没有任何已知SL伙伴的新基因进行准确预测也极具挑战性。

结果

在这项工作中,我们提出了一种名为GCATSL的新型图上下文注意力网络来学习用于SL预测的基因表示。首先,我们利用不同的数据源为基因构建多个特征图,这些图作为我们的GCATSL方法的特征输入。其次,对于每个特征图,我们设计节点级注意力机制以有效捕捉局部和全局邻居的重要性,并分别学习节点的局部和全局表示。我们进一步利用多层感知器(MLP)将原始特征与局部和全局表示进行聚合,然后得出特定于特征的表示。第三,为了得出最终表示,我们设计特征级注意力以通过考虑不同特征图的重要性来整合特定于特征的表示。在不同设置下对三个数据集进行的广泛实验结果表明,我们的GCATSL模型始终优于14种先进方法。此外,案例研究进一步验证了我们提出的模型在识别新型SL对方面的有效性。

可用性和实现

Python代码和数据集可在GitHub(https://github.com/longyahui/GCATSL)和Zenodo(https://zenodo.org/record/4522679)上根据MIT许可免费获取。

补充信息

补充数据可在《生物信息学》在线获取。

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