Deep learning for extracting protein-protein interactions from biomedical literature

Yifan Peng, Zhiyong Lu
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引用次数: 93

Abstract

State-of-the-art methods for protein-protein interaction (PPI) extraction are primarily feature-based or kernel-based by leveraging lexical and syntactic information. But how to incorporate such knowledge in the recent deep learning methods remains an open question. In this paper, we propose a multichannel dependency-based convolutional neural network model (McDepCNN). It applies one channel to the embedding vector of each word in the sentence, and another channel to the embedding vector of the head of the corresponding word. Therefore, the model can use richer information obtained from different channels. Experiments on two public benchmarking datasets, AIMed and BioInfer, demonstrate that McDepCNN provides up to 6% F1-score improvement over rich feature-based methods and single-kernel methods. In addition, McDepCNN achieves 24.4% relative improvement in F1-score over the state-of-the-art methods on cross-corpus evaluation and 12% improvement in F1-score over kernel-based methods on “difficult” instances. These results suggest that McDepCNN generalizes more easily over different corpora, and is capable of capturing long distance features in the sentences.
从生物医学文献中提取蛋白质-蛋白质相互作用的深度学习
蛋白质-蛋白质相互作用(PPI)提取的最新方法主要是基于特征或基于核的,利用词汇和句法信息。但是如何将这些知识融入到最近的深度学习方法中仍然是一个悬而未决的问题。在本文中,我们提出了一个基于多通道依赖的卷积神经网络模型(McDepCNN)。它将一个通道应用于句子中每个单词的嵌入向量,另一个通道应用于相应单词头部的嵌入向量。因此,该模型可以利用从不同渠道获得的更丰富的信息。在两个公共基准测试数据集(aims和BioInfer)上的实验表明,与基于丰富特征的方法和单核方法相比,McDepCNN提供了高达6%的f1分数提升。此外,McDepCNN在跨语料库评估上的f1分数比最先进的方法提高了24.4%,在“困难”实例上的f1分数比基于核的方法提高了12%。这些结果表明McDepCNN更容易在不同的语料库上进行泛化,并且能够捕获句子中的长距离特征。
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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