A deep learning algorithm for predicting protein-protein interactions with nonnegative latent factorization

Liwei Wang, Lun Hu
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引用次数: 1

Abstract

Protein-protein interaction (PPI) networks play an essential role in the study of proteomics. Given the fact that known PPI data are extremely incomplete, high-throughput technologies have been developed to significantly increase the amount of PPI data, but they are prone to generate false positive PPIs and accordingly affect the performance of computational prediction algorithms. To overcome this problem, we propose a novel deep learning algorithm for predicting PPIs with symmetric nonnegative latent factorization (SNLF). In particular, we first improve the quality of PPI data by applying an established SNLF model. Quasi-Sequence-Order is then used to encode proteins based on the modality of their sequence information. Principal component analysis is utilized to generate the features of proteins in a more compact manner. After that, we adopt graph variational autoencoder to learn the embedding of each protein by considering protein features and network topology. Finally, the embeddings of proteins are concatenated in pairs as input to train a simple feedforward neural network for prediction. Experiments have been performed on five different PPI datasets by comparing the performance of our algorithm with the state-of-the-art prediction algorithms, and the results demonstrate that the proposed model is promising in predicting PPIs.
基于非负潜因子分解的蛋白质相互作用预测的深度学习算法
蛋白质-蛋白质相互作用网络在蛋白质组学研究中起着至关重要的作用。鉴于已知PPI数据极其不完整,高通量技术的发展大大增加了PPI数据量,但它们容易产生假阳性PPI,从而影响计算预测算法的性能。为了克服这个问题,我们提出了一种新的深度学习算法,用于对称非负潜分解(SNLF)预测ppi。特别是,我们首先通过应用已建立的SNLF模型来提高PPI数据的质量。然后根据序列信息的模态使用准序列顺序对蛋白质进行编码。利用主成分分析以更紧凑的方式生成蛋白质的特征。然后,结合蛋白质特征和网络拓扑结构,采用图变分自编码器学习每个蛋白质的嵌入。最后,将嵌入的蛋白质成对连接作为输入,训练一个简单的前馈神经网络进行预测。在5个不同PPI数据集上进行了实验,并将该算法与最先进的预测算法的性能进行了比较,结果表明该模型在PPI预测方面是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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