Specificity of SARS-CoV-2 Real-Time PCR Improved by Deep Learning Analysis.

Journal: Journal of clinical microbiology
Published Date:

Abstract

Real-time PCR (RT-PCR) is widely used to diagnose human pathogens. RT-PCR data are traditionally analyzed by estimating the threshold cycle ( ) at which the fluorescence signal produced by emission of a probe crosses a baseline level. Current models used to estimate the value are based on approximations that do not adequately account for the stochastic variations of the fluorescence signal that is detected during RT-PCR. Less common deviations become more apparent as the sample size increases, as is the case in the current SARS-CoV-2 pandemic. In this work, we employ a method independent of value to interpret RT-PCR data. In this novel approach, we built and trained a deep learning model, qPCRdeepNet, to analyze the fluorescent readings obtained during RT-PCR. We describe how this model can be deployed as a quality assurance tool to monitor result interpretation in real time. The model's performance with the TaqPath COVID19 Combo Kit assay, widely used for SARS-CoV-2 detection, is described. This model can be applied broadly for the primary interpretation of RT-PCR assays and potentially replace the interpretive paradigm.

Authors

  • David J Alouani
    Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA.
  • Roshani R P Rajapaksha
    Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA.
  • Mehul Jani
    Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA.
  • Daniel D Rhoads
    Department of Pathology, Case Western Reserve University, Cleveland, Ohio, USA daniel.rhoads@case.edu.
  • Navid Sadri
    Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA navid.sadri@uhhospitals.org.