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The dilution linearity of the calibration curve was maintained at five orders of magnitude 1.0× 10 to 1.0×10 copies/μL, and was confirmed to be detectable down to 1.0×10 copies/μL. The limit of quantification of RNA extracted from clinical specimens using RT-LAMP correlated well with that obtained using RT-qPCR (r =0.93. The findings indicate that RT-LAMP is an effective method to determine the viral load of SARS-CoV-2. The findings indicate that RT-LAMP is an effective method to determine the viral load of SARS-CoV-2. This study inve
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