Variational Autoencoder Based Network Embedding Algorithm For Protein Function Prediction

Guansong Cao, Yuan Zhu, Ming Yi
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引用次数: 1

Abstract

The development of high-throughput technology has produced a large number of protein-protein interaction datasets, which provide an effective way to infer the functional annotation of proteins. However, how to make proper use of these datasets to extract effective low-dimensional feature representation of proteins for functional prediction is a challenge. Most existing network integration methods for protein function prediction have some limitations to capture complex and highly non-linear network structure information due to their design architecture. Therefore, we propose a novel multi-network embedding method deepVAE based on deep variational autoencoder (VAE), which uses the variational autoencoder to extract low-dimensional features of proteins from multiple various interactive network datasets and then trains a SVM classifier to predict protein function. Particularly, we denoise the original networks before network embedding, thus the new proposed method is called deepVAE-NE. The experiments are conducted on the yeast and human protein-protein interaction datasets and the experimental performance shows that our methods perform better than the other four compared advanced approaches, which greatly improves the accuracy of functional prediction.
基于变分自编码器的蛋白质功能预测网络嵌入算法
高通量技术的发展产生了大量蛋白质-蛋白质相互作用数据集,为推断蛋白质的功能注释提供了有效途径。然而,如何正确地利用这些数据集提取有效的蛋白质低维特征表示来进行功能预测是一个挑战。现有的用于蛋白质功能预测的网络集成方法由于其设计结构的限制,在捕获复杂和高度非线性的网络结构信息时存在一定的局限性。因此,我们提出了一种基于深度变分自编码器(deep variational autoencoder, VAE)的新型多网络嵌入方法deepVAE,该方法利用变分自编码器从多个不同的交互网络数据集中提取蛋白质的低维特征,然后训练SVM分类器来预测蛋白质功能。特别地,我们在网络嵌入之前对原始网络进行了去噪,因此我们提出的新方法被称为deepvee - ne。在酵母和人类蛋白-蛋白相互作用数据集上进行了实验,实验结果表明,我们的方法优于其他四种比较先进的方法,大大提高了功能预测的准确性。
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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