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      Machine Learning-Assisted Real-Time Polymerase Chain Reaction and High-Resolution Melt Analysis for SARS-CoV-2 Variant Identification

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          Abstract

          Since the declaration of COVID-19 as a pandemic in early 2020, multiple variants of the severe acute respiratory syndrome-related coronavirus (SARS-CoV-2) have been detected. The emergence of multiple variants has raised concerns due to their impact on public health. Therefore, it is crucial to distinguish between different viral variants. Here, we developed a machine learning web-based application for SARS-CoV-2 variant identification via duplex real-time polymerase chain reaction (PCR) coupled with high-resolution melt (qPCR-HRM) analysis. As a proof-of-concept, we investigated the platform’s ability to identify the Alpha, Delta, and wild-type strains using two sets of primers. The duplex qPCR-HRM could identify the two variants reliably in as low as 100 copies/μL. Finally, the platform was validated with 167 nasopharyngeal swab samples, which gave a sensitivity of 95.2%. This work demonstrates the potential for use as automated, cost-effective, and large-scale viral variant surveillance.

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          Most cited references45

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          Neutralising antibody activity against SARS-CoV-2 VOCs B.1.617.2 and B.1.351 by BNT162b2 vaccination

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            Is Open Access

            Rapid electrochemical detection of coronavirus SARS-CoV-2

            Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which is time-consuming and requires expensive instrumentation. Here, we report an ultrasensitive electrochemical biosensor based on isothermal rolling circle amplification (RCA) for rapid detection of SARS-CoV-2. The assay involves the hybridization of the RCA amplicons with probes that were functionalized with redox active labels that are detectable by an electrochemical biosensor. The one-step sandwich hybridization assay could detect as low as 1 copy/μL of N and S genes, in less than 2 h. Sensor evaluation with 106 clinical samples, including 41 SARS-CoV-2 positive and 9 samples positive for other respiratory viruses, gave a 100% concordance result with qRT-PCR, with complete correlation between the biosensor current signals and quantitation cycle (Cq) values. In summary, this biosensor could be used as an on-site, real-time diagnostic test for COVID-19.
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              iSCAN: An RT-LAMP-coupled CRISPR-Cas12 module for rapid, sensitive detection of SARS-CoV-2

              Highlights • RT-LAMP coupled with CRISPR-Cas12 provides a sensitive and specific virus detection platform. • iSCAN sensitivity and specificity are comparable with RT-qPCR. • iSCAN is a 1 hr detection module that can help in testing in low resource areas. • iSCAN can be developed as a one-pot assay. • iSCAN reagents can be produced locally and deployed for SARS-CoV2 detection.
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                Author and article information

                Journal
                Anal Chem
                Anal Chem
                ac
                ancham
                Analytical Chemistry
                American Chemical Society
                0003-2700
                1520-6882
                12 January 2023
                24 January 2023
                : 95
                : 3
                : 2102-2109
                Affiliations
                []Department of Biomedical Engineering, Faculty of Engineering, Mahidol University , Salaya 73170, Nakhon Pathom, Thailand
                []Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University , Bangkok 10330, Thailand
                [§ ]Faculty of Applied Sciences, AIMST University , Bedong, Kedah 08100, Malaysia
                []Integrative Computational BioScience (ICBS) Center, Mahidol University , Salaya 73170, Nakhon Pathom, Thailand
                Author notes
                Author information
                https://orcid.org/0000-0003-0086-8371
                Article
                10.1021/acs.analchem.2c05112
                9843624
                36633573
                915f601e-a254-4a4b-bf0e-86560e6f64b8
                © 2023 American Chemical Society

                This article is made available via the PMC Open Access Subset for unrestricted RESEARCH re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 16 November 2022
                : 29 December 2022
                Funding
                Funded by: Chulalongkorn University, doi 10.13039/501100002873;
                Award ID: NA
                Funded by: Urban Disease Control and Prevention, doi NA;
                Award ID: NA
                Funded by: National Research Council of Thailand, doi 10.13039/501100004704;
                Award ID: NA
                Categories
                Article
                Custom metadata
                ac2c05112
                ac2c05112

                Analytical chemistry
                Analytical chemistry

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