Identification of bacteriophage genome sequences with representation learning

Author:

Bai Zeheng1ORCID,Zhang Yao-zhong1,Miyano Satoru12,Yamaguchi Rui134,Fujimoto Kosuke56,Uematsu Satoshi56,Imoto Seiya16ORCID

Affiliation:

1. Division of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo , Minato-ku, Tokyo 108-8639, Japan

2. M&D Data Science Center, Tokyo Medical and Dental University , Tokyo 113-8510, Japan

3. Division of Cancer Systems Biology, Aichi Cancer Center Research Institute , Nagoya 464-8681, Japan

4. Division of Cancer Informatics, Nagoya University Graduate School of Medicine , Nagoya 466-8560, Japan

5. Division of Metagenome Medicine, Human Genome Center, The Institute of Medical Science, The University of Tokyo , Minato-ku, Tokyo 108-8639, Japan

6. Collaborative Research Institute for Innovative Microbiology, The University of Tokyo , Bunkyo-ku, Tokyo 113-8657, Japan

Abstract

Abstract Motivation Bacteriophages/phages are the viruses that infect and replicate within bacteria and archaea, and rich in human body. To investigate the relationship between phages and microbial communities, the identification of phages from metagenome sequences is the first step. Currently, there are two main methods for identifying phages: database-based (alignment-based) methods and alignment-free methods. Database-based methods typically use a large number of sequences as references; alignment-free methods usually learn the features of the sequences with machine learning and deep learning models. Results We propose INHERIT which uses a deep representation learning model to integrate both database-based and alignment-free methods, combining the strengths of both. Pre-training is used as an alternative way of acquiring knowledge representations from existing databases, while the BERT-style deep learning framework retains the advantage of alignment-free methods. We compare INHERIT with four existing methods on a third-party benchmark dataset. Our experiments show that INHERIT achieves a better performance with the F1-score of 0.9932. In addition, we find that pre-training two species separately helps the non-alignment deep learning model make more accurate predictions. Availability and implementation The codes of INHERIT are now available in: https://github.com/Celestial-Bai/INHERIT. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Ministry of Education, Culture, Sports, Science, and Technology of Japan

Japan Society for the Promotion of Science

JSPS KAKENHI

Japan Agency for Medical Research and Development

Uehara Memorial Foundation

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference48 articles.

1. Antibiotic resistance and its cost: is it possible to reverse resistance?;Andersson;Nat. Rev. Microbiol,2010

2. Seeker: alignment-free identification of bacteriophage genomes by deep learning;Auslander;Nucleic Acids Res,2020

3. Representation learning: a review and new perspectives;Bengio;IEEE Trans. Pattern Anal. Mach. Intell,2013

4. Phages and their application against drug-resistant bacteria;Chanishvili;J. Chem. Technol. Biotechnol,2001

5. Multiple sequence alignment modeling: methods and applications;Chatzou;Brief. Bioinform,2016

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3