Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains
The influenza pandemics have caused millions of deaths and enormous economic loss. Current circulating influenza viruses in human, avian, swine and other animals are potential to evolve into novel strains that may cause another pandemic in the future. Hence, recognizing the determinants of pandemic...
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sg-ntu-dr.10356-1025112020-03-07T11:48:50Z Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains Yin, Rui Fransiskus, Xaverius Ivan Zheng, Jie Zhou, Xinrui Chow, Vincent T. K. Kwoh, Chee Keong School of Computer Science and Engineering Proceedings of the 6th International Conference on Bioinformatics and Biomedical Science Singapore Internet Research Centre Bioinformatics Research Centre Engineering::Computer science and engineering Influenza A Virus Pandemic The influenza pandemics have caused millions of deaths and enormous economic loss. Current circulating influenza viruses in human, avian, swine and other animals are potential to evolve into novel strains that may cause another pandemic in the future. Hence, recognizing the determinants of pandemic strains helps to raise the alarm of future pandemics. With increasingly huge biological data, computational modeling is a good technique for analyzing data, providing novel insight into significant patterns and rules. Here we define a binary classification problem of categorizing influenza strains into pandemic and non-pandemic classes based on amino acid sequences. Three rule-based algorithms are applied, namely OneR, JRip and PART, to extract rules, composed of potential critical virulent sites. The results present good performance in term of accuracy, specificity, sensitivity and F-measure (more than 0.9 on average for each). Fourteen out of the sixteen potential critical virulent sites detected in our experiments are overlapped with receptor binding sites or antigenic sites. In addition, some variations occurred in these sites are known to affect the pathogenicity of influenza viruses or to cause more severe symptom in the infected patients. The pandemic potential of uncovered sites in our study needs to be further experimentally validated. MOE (Min. of Education, S’pore) Accepted version 2019-08-28T01:52:47Z 2019-12-06T20:56:09Z 2019-08-28T01:52:47Z 2019-12-06T20:56:09Z 2017 Conference Paper Yin, R., Zhou, X., Fransiskus, X. I., Zheng, J., Chow, V. T. K., & Kwoh, C. K. (2017). Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains. Proceedings of the 6th International Conference on Bioinformatics and Biomedical Science - ICBBS '17. doi:10.1145/3121138.3121166 https://hdl.handle.net/10356/102511 http://hdl.handle.net/10220/49803 10.1145/3121138.3121166 en © 2017 Association for Computing Machinery (ACM). All rights reserved. This paper was published in Proceedings of the 6th International Conference on Bioinformatics and Biomedical Science and is made available with permission of Association for Computing Machinery (ACM). 8 p. application/pdf |
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Engineering::Computer science and engineering Influenza A Virus Pandemic Yin, Rui Fransiskus, Xaverius Ivan Zheng, Jie Zhou, Xinrui Chow, Vincent T. K. Kwoh, Chee Keong Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains |
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The influenza pandemics have caused millions of deaths and enormous economic loss. Current circulating influenza viruses in human, avian, swine and other animals are potential to evolve into
novel strains that may cause another pandemic in the future. Hence, recognizing the determinants of pandemic strains helps to raise the alarm of future pandemics. With increasingly huge biological data, computational modeling is a good technique for analyzing data, providing novel insight into significant patterns and rules. Here we define a binary classification problem of categorizing influenza strains into pandemic and non-pandemic
classes based on amino acid sequences. Three rule-based
algorithms are applied, namely OneR, JRip and PART, to extract
rules, composed of potential critical virulent sites. The results
present good performance in term of accuracy, specificity,
sensitivity and F-measure (more than 0.9 on average for each).
Fourteen out of the sixteen potential critical virulent sites detected
in our experiments are overlapped with receptor binding sites or
antigenic sites. In addition, some variations occurred in these sites
are known to affect the pathogenicity of influenza viruses or to
cause more severe symptom in the infected patients. The
pandemic potential of uncovered sites in our study needs to be
further experimentally validated. |
author2 |
School of Computer Science and Engineering |
author_facet |
School of Computer Science and Engineering Yin, Rui Fransiskus, Xaverius Ivan Zheng, Jie Zhou, Xinrui Chow, Vincent T. K. Kwoh, Chee Keong |
format |
Conference or Workshop Item |
author |
Yin, Rui Fransiskus, Xaverius Ivan Zheng, Jie Zhou, Xinrui Chow, Vincent T. K. Kwoh, Chee Keong |
author_sort |
Yin, Rui |
title |
Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains |
title_short |
Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains |
title_full |
Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains |
title_fullStr |
Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains |
title_full_unstemmed |
Identification of potential critical virulent sites based on hemagglutinin of influenza A virus in past pandemic strains |
title_sort |
identification of potential critical virulent sites based on hemagglutinin of influenza a virus in past pandemic strains |
publishDate |
2019 |
url |
https://hdl.handle.net/10356/102511 http://hdl.handle.net/10220/49803 |
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1681049282113699840 |