Correction to: Virologica Sinica https://doi.org/10.1007/s12250-020-00218-1
In the original version of this article, the legend to Figure 1 was incorrect. The corrected legend is given below.
Fig. 1 A Location of the primers in SARS-CoV-2 genome. B Sequence comparison among seven human coronaviruses (SARS-CoV-2, SARS-CoV, MERS-CoV, HCoVOC43, HCoV-HKU-1, HCoV-NL63 and HCoV-229E). C Cross-reactivity test of the novel SARS-CoV-2 RTLAMP assay to other common respiratory viruses. Tested common respiratory viruses include HCoV-HKU-1, HCoV-NL63, HCoV-OC43, HCoV-229E, influenza A, B, and C viruses, parainfluenza viruses type 1-3, enterovirus, respiratory syncytial virus A and B groups, human rhinovirus, human metapneumovirus, adenovirus and bocavirus. RNA from a COVID-19 patient was used as positive control (PC). D Sensitivity test of the novel SARS-CoV-2 RT-LAMP assay. Positive amplification was defined only when two replicates are successfully amplified. E Visual detection of SARS-CoV-2 by the colorimetric RT-LAMP assay. E-a RNA standards; E-b Clinical samples. NTC: non-template control
Correction to: Development of a Novel Reverse Transcription Loop-Mediated Isothermal Amplification Method for Rapid Detection of SARS-CoV-2
- Published Date: 23 April 2020