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SARS2020: an integrated platform for identification of novel coronavirus by a consensus sequence-function model
Dachuan Zhang1, Tong Zhang1, Sheng Liu1
1CAS Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200333, P. R. China.
Bioinformatics (Oxford, England)
|September 2, 2020
Summary
A new resource, SARS2020, aids in identifying viruses by their encoded enzymes. This approach identified the novel coronavirus
Area of Science:
- Virology
- Bioinformatics
- Drug Discovery
Background:
- The 2019 novel coronavirus outbreak poses a significant global health challenge.
- Predicting pathogen biological function from genomic sequences is crucial for effective response.
- Identifying viruses based on their encoded enzymes, essential for propagation, remains underexplored.
Purpose of the Study:
- To develop a comprehensive resource for coronavirus research.
- To establish a sequence-based method for virus identification.
- To aid in the rapid identification of future epidemic agents.
Main Methods:
- Integrated coronavirus research, genomic sequences, and antiviral drug trial results into the SARS2020 resource.
- Developed a consensus sequence-catalytic function model.
- Utilized a data-driven, sequence-based strategy for virus identification.
Main Results:
- The SARS2020 resource provides a centralized platform for coronavirus data.
- The sequence-catalytic function model identified the novel coronavirus as encoding the same proteinase as SARS-CoV.
- The study demonstrates a novel strategy for rapid pathogen identification.
Conclusions:
- The SARS2020 resource and the developed model offer a valuable tool for virological research.
- Sequence-based identification of viral enzymes is a promising strategy for future epidemic preparedness.
- This approach facilitates rapid identification and characterization of novel viral threats.

