4.6 Article

iDNA-MT: Identification DNA Modification Sites in Multiple Species by Using Multi-Task Learning Based a Neural Network Tool

期刊

FRONTIERS IN GENETICS
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.663572

关键词

multi-task learning; DNA modification; feature representation; deep learning; neural network

资金

  1. New Energy and Industrial Technology Development Organization 265 (NEDO)
  2. Japan Society for the Promotion of Science (JSPS) [18H03250]
  3. Natural Science Foundation of China
  4. Grants-in-Aid for Scientific Research [18H03250] Funding Source: KAKEN

向作者/读者索取更多资源

This study proposed a computational method, iDNA-MT, to identify 4mC sites and 6mA sites in multiple species. Experimental results show that iDNA-MT outperforms other state-of-the-art single-task methods for identifying 4mA or 6mC sites in multiple species. The promising results demonstrate that iDNA-MT has great potential to be a powerful and practically useful tool for accurately identifying DNA modifications.
Motivation DNA N4-methylcytosine (4mC) and N6-methyladenine (6mA) are two important DNA modifications and play crucial roles in a variety of biological processes. Accurate identification of the modifications is essential to better understand their biological functions and mechanisms. However, existing methods to identify 4mA or 6mC sites are all single tasks, which demonstrates that they can identify only a certain modification in one species. Therefore, it is desirable to develop a novel computational method to identify the modification sites in multiple species simultaneously. Results In this study, we proposed a computational method, called iDNA-MT, to identify 4mC sites and 6mA sites in multiple species, respectively. The proposed iDNA-MT mainly employed multi-task learning coupled with the bidirectional gated recurrent units (BGRU) to capture the sharing information among different species directly from DNA primary sequences. Experimental comparative results on two benchmark datasets, containing different species respectively, show that either for identifying 4mA or for 6mC site in multiple species, the proposed iDNA-MT outperforms other state-of-the-art single-task methods. The promising results have demonstrated that iDNA-MT has great potential to be a powerful and practically useful tool to accurately identify DNA modifications.

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