DLPAlign:一种基于深度学习的多蛋白质序列渐进比对方法

Mengmeng Kuang, Yong Liu, Lufei Gao
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引用次数: 4

摘要

本文提出了一种新颖、直观的方法来提高渐进式多蛋白序列比对方法的准确性。我们基于卷积神经网络和双向长短期记忆网络训练了一个决策模型,并通过计算不同的后验概率矩阵逐步对齐输入的蛋白质序列。为了评估该方法,我们实现了一个名为DLPAlign的多序列比对工具,并在三个经验比对基准(BAliBASE, OXBench和SABMark)上将其性能与11种领先的比对方法进行了比较。我们的结果表明,DLPAlign可以在三个基准测试中获得最佳的总列分数。当对平均PID≤30%的711个低相似性家族进行评估时,DLPAlign比第二好的MSA软件提高了约2.8%。此外,我们比较了DLPAlign与其他比对工具在实际应用中的性能,即对4个与SARS-COV-2相关的蛋白质序列进行蛋白质二级结构预测,在所有情况下,DLPAlign都提供了最好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DLPAlign: A Deep Learning based Progressive Alignment Method for Multiple Protein Sequences
This paper proposed a novel and straightforward approach to improve the accuracy of progressive multiple protein sequence alignment method. We trained a decision-making model based on the convolutional neural networks and bi-directional long short term memory networks, and progressively aligned the input protein sequences by calculating different posterior probability matrices. To evaluate this method, we have implemented a multiple sequence alignment tool called DLPAlign and compared its performance with eleven leading alignment methods on three empirical alignment benchmarks (BAliBASE, OXBench and SABMark). Our results show that DLPAlign can get the best total-column scores on the three benchmarks. When evaluated against the 711 low similarity families with average PID ≤ 30%, DLPAlign improved about 2.8% over the second-best MSA software. Besides, we compared the performance of DLPAlign and other alignment tools on a real-life application, namely protein secondary structure prediction on four protein sequences related to SARS-COV-2, and DLPAlign provides the best result in all cases.
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