DeepRaccess:使用深度学习的高速RNA可及性预测

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Kaisei Hara, Natsuki Iwano, Tsukasa Fukunaga, Michiaki Hamada
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引用次数: 0

摘要

RNA可及性是预测原核生物RNA-RNA相互作用和翻译效率的一个有用的RNA二级结构特征。然而,传统的可及性计算工具,如Raccess,在计算上是昂贵的,并且需要大量的计算时间来执行转录组规模的分析。在这项研究中,我们开发了基于深度学习方法预测RNA可及性的DeepRaccess。DeepRaccess训练将人工RNA序列作为输入,并根据Raccess计算的结果预测这些序列的可及性。模拟和实证数据分析表明,DeepRaccess预测的可达性与Raccess计算的可达性高度相关。此外,我们证实了DeepRaccess可以从开始密码子周围的序列预测大肠杆菌中的蛋白质丰度,准确度中等。我们还证明了DeepRaccess在GPU环境下实现了数十到数百倍的软件加速。DeepRaccess的源代码和训练模型可在https://github.com/hmdlab/DeepRaccess免费获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DeepRaccess: high-speed RNA accessibility prediction using deep learning
RNA accessibility is a useful RNA secondary structural feature for predicting RNA-RNA interactions and translation efficiency in prokaryotes. However, conventional accessibility calculation tools, such as Raccess, are computationally expensive and require considerable computational time to perform transcriptome-scale analyses. In this study, we developed DeepRaccess, which predicts RNA accessibility based on deep learning methods. DeepRaccess was trained to take artificial RNA sequences as input and to predict the accessibility of these sequences as calculated by Raccess. Simulation and empirical dataset analyses showed that the accessibility predicted by DeepRaccess was highly correlated with the accessibility calculated by Raccess. In addition, we confirmed that DeepRaccess can predict protein abundance in E.coli with moderate accuracy from the sequences around the start codon. We also demonstrated that DeepRaccess achieved tens to hundreds of times software speed-up in a GPU environment. The source codes and the trained models of DeepRaccess are freely available at https://github.com/hmdlab/DeepRaccess.
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CiteScore
2.60
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