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AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease

Global pandemics such as COVID-19 have resulted in significant global social and economic disruption. Although polymerase chain reaction (PCR) is recommended as the standard test for identifying the SARS-CoV-2, conventional assays are time-consuming. In parallel, although artificial intelligence (AI...

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Autores principales: Sun, Hao, Xiong, Linghu, Huang, Yi, Chen, Xinkai, Yu, Yongjian, Ye, Shaozhen, Dong, Hui, Jia, Yuan, Zhang, Wenwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Publishing Services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712671/
http://dx.doi.org/10.1016/j.fmre.2021.12.005
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author Sun, Hao
Xiong, Linghu
Huang, Yi
Chen, Xinkai
Yu, Yongjian
Ye, Shaozhen
Dong, Hui
Jia, Yuan
Zhang, Wenwei
author_facet Sun, Hao
Xiong, Linghu
Huang, Yi
Chen, Xinkai
Yu, Yongjian
Ye, Shaozhen
Dong, Hui
Jia, Yuan
Zhang, Wenwei
author_sort Sun, Hao
collection PubMed
description Global pandemics such as COVID-19 have resulted in significant global social and economic disruption. Although polymerase chain reaction (PCR) is recommended as the standard test for identifying the SARS-CoV-2, conventional assays are time-consuming. In parallel, although artificial intelligence (AI) has been employed to contain the disease, the implementation of AI in PCR analytics, which may enhance the cognition of diagnostics, is quite rare. The information that the amplification curve reveals can reflect the dynamics of reactions. Here, we present a novel AI-aided on-chip approach by integrating deep learning with microfluidic paper-based analytical devices (µPADs) to detect synthetic RNA templates of the SARS-CoV-2 ORF1ab gene. The µPADs feature a multilayer structure by which the devices are compatible with conventional PCR instruments. During analysis, real-time PCR data were synchronously fed to three unsupervised learning models with deep neural networks, including RNN, LSTM, and GRU. Of these, the GRU is found to be most effective and accurate. Based on the experimentally obtained datasets, qualitative forecasting can be made as early as 13 cycles, which significantly enhances the efficiency of the PCR tests by 67.5% (∼40 min). Also, an accurate prediction of the end-point value of PCR curves can be obtained by GRU around 20 cycles. To further improve PCR testing efficiency, we also propose AI-aided dynamic evaluation criteria for determining critical cycle numbers, which enables real-time quantitative analysis of PCR tests. The presented approach is the first to integrate AI for on-chip PCR data analysis. It is capable of forecasting the final output and the trend of qPCR in addition to the conventional end-point Cq calculation. It is also capable of fully exploring the dynamics and intrinsic features of each reaction. This work leverages methodologies from diverse disciplines to provide perspectives and insights beyond the scope of a single scientific field. It is universally applicable and can be extended to multiple areas of fundamental research.
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spelling pubmed-87126712021-12-28 AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease Sun, Hao Xiong, Linghu Huang, Yi Chen, Xinkai Yu, Yongjian Ye, Shaozhen Dong, Hui Jia, Yuan Zhang, Wenwei Fundamental Research Article Global pandemics such as COVID-19 have resulted in significant global social and economic disruption. Although polymerase chain reaction (PCR) is recommended as the standard test for identifying the SARS-CoV-2, conventional assays are time-consuming. In parallel, although artificial intelligence (AI) has been employed to contain the disease, the implementation of AI in PCR analytics, which may enhance the cognition of diagnostics, is quite rare. The information that the amplification curve reveals can reflect the dynamics of reactions. Here, we present a novel AI-aided on-chip approach by integrating deep learning with microfluidic paper-based analytical devices (µPADs) to detect synthetic RNA templates of the SARS-CoV-2 ORF1ab gene. The µPADs feature a multilayer structure by which the devices are compatible with conventional PCR instruments. During analysis, real-time PCR data were synchronously fed to three unsupervised learning models with deep neural networks, including RNN, LSTM, and GRU. Of these, the GRU is found to be most effective and accurate. Based on the experimentally obtained datasets, qualitative forecasting can be made as early as 13 cycles, which significantly enhances the efficiency of the PCR tests by 67.5% (∼40 min). Also, an accurate prediction of the end-point value of PCR curves can be obtained by GRU around 20 cycles. To further improve PCR testing efficiency, we also propose AI-aided dynamic evaluation criteria for determining critical cycle numbers, which enables real-time quantitative analysis of PCR tests. The presented approach is the first to integrate AI for on-chip PCR data analysis. It is capable of forecasting the final output and the trend of qPCR in addition to the conventional end-point Cq calculation. It is also capable of fully exploring the dynamics and intrinsic features of each reaction. This work leverages methodologies from diverse disciplines to provide perspectives and insights beyond the scope of a single scientific field. It is universally applicable and can be extended to multiple areas of fundamental research. The Authors. Publishing Services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. 2022-05 2021-12-28 /pmc/articles/PMC8712671/ http://dx.doi.org/10.1016/j.fmre.2021.12.005 Text en © 2021 The Authors. Publishing Services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights 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 free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Sun, Hao
Xiong, Linghu
Huang, Yi
Chen, Xinkai
Yu, Yongjian
Ye, Shaozhen
Dong, Hui
Jia, Yuan
Zhang, Wenwei
AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
title AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
title_full AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
title_fullStr AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
title_full_unstemmed AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
title_short AI-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
title_sort ai-aided on-chip nucleic acid assay for smart diagnosis of infectious disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712671/
http://dx.doi.org/10.1016/j.fmre.2021.12.005
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