Deep Ensemble Learning with Atrous Spatial Pyramid Networks for Protein Secondary Structure Prediction

被引:3
|
作者
Guo, Yuzhi [1 ]
Wu, Jiaxiang [2 ]
Ma, Hehuan [1 ]
Wang, Sheng [1 ]
Huang, Junzhou [1 ]
机构
[1] Univ Texas Arlington, Dept Comp Sci & Engn, Arlington, TX 76019 USA
[2] Tencent, Al Lab, Shenzhen 508929, Peoples R China
关键词
deep learning; protein secondary structure prediction; learning representation; computational biology; NEURAL-NETWORKS; SEGMENTATION;
D O I
10.3390/biom12060774
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The secondary structure of proteins is significant for studying the three-dimensional structure and functions of proteins. Several models from image understanding and natural language modeling have been successfully adapted in the protein sequence study area, such as Long Short-term Memory (LSTM) network and Convolutional Neural Network (CNN). Recently, Gated Convolutional Neural Network (GCNN) has been proposed for natural language processing. It has achieved high levels of sentence scoring, as well as reduced the latency. Conditionally Parameterized Convolution (CondConv) is another novel study which has gained great success in the image processing area. Compared with vanilla CNN, CondConv uses extra sample-dependant modules to conditionally adjust the convolutional network. In this paper, we propose a novel Conditionally Parameterized Convolutional network (CondGCNN) which utilizes the power of both CondConv and GCNN. CondGCNN leverages an ensemble encoder to combine the capabilities of both LSTM and CondGCNN to encode protein sequences by better capturing protein sequential features. In addition, we explore the similarity between the secondary structure prediction problem and the image segmentation problem, and propose an ASP network (Atrous Spatial Pyramid Pooling (ASPP) based network) to capture fine boundary details in secondary structure. Extensive experiments show that the proposed method can achieve higher performance on protein secondary structure prediction task than existing methods on CB513, Casp11, CASP12, CASP13, and CASP14 datasets. We also conducted ablation studies over each component to verify the effectiveness. Our method is expected to be useful for any protein related prediction tasks, which is not limited to protein secondary structure prediction.
引用
收藏
页数:16
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