Deep transformers and convolutional neural network in identifying DNA N6-methyladenine sites in cross-species genomes

被引:73
|
作者
Le, Nguyen Quoc Khanh [1 ,2 ,3 ]
Ho, Quang-Thai [4 ,5 ]
机构
[1] Taipei Med Univ, Coll Med, Profess Master Program Artificial Intelligence Med, Taipei 106, Taiwan
[2] Taipei Med Univ, Res Ctr Artificial Intelligence Med, Taipei 106, Taiwan
[3] Taipei Med Univ Hosp, Translat Imaging Res Ctr, Taipei 110, Taiwan
[4] Can Tho Univ, Coll Informat & Commun Technol, Can Tho, Vietnam
[5] Yuan Ze Univ, Dept Comp Sci & Engn, Chungli 32003, Taiwan
关键词
N6-methyladenine site; Post-translational modification; Natural language processing; Deep learning; DNA sequence analysis; Contextualized word embedding; IDENTIFICATION; TOOL;
D O I
10.1016/j.ymeth.2021.12.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As one of the most common post-transcriptional epigenetic modifications, N6-methyladenine (6 mA), plays an essential role in various cellular processes and disease pathogenesis. Therefore, accurately identifying 6 mA modifications is necessary for a deep understanding of cellular processes and other possible functional mechanisms. Although a few computational methods have been proposed, their respective models were developed with small training datasets. Hence, their practical application is quite limited in genome-wide detection. To overcome the existing limitations, we present a novel model based on transformer architecture and deep learning to identify DNA 6 mA sites from the cross-species genome. The model is constructed on a benchmark dataset and explored a feature derived from pre-trained transformer word embedding approaches. Subsequently, a convolutional neural network was employed to learn the generated features and generate the prediction outcomes. As a result, our predictor achieved excellent performance during independent test with the accuracy and Matthews correlation coefficient (MCC) of 79.3% and 0.58, respectively. Overall, its performance achieved better accuracy than the baseline models and significantly outperformed the existing predictors, demonstrating the effectiveness of our proposed hybrid framework. Furthermore, our model is expected to assist biologists in accurately identifying 6mAs and formulate the novel testable biological hypothesis. We also release source codes and datasets freely at https://github.com/khanhlee/bert-dna for front-end users.
引用
收藏
页码:199 / 206
页数:8
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