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. 2020 Apr 23;35(4):499. doi: 10.1007/s12250-020-00223-4

Correction to: Development of a Novel Reverse Transcription Loop-Mediated Isothermal Amplification Method for Rapid Detection of SARS-CoV-2

Renfei Lu 1, Xiuming Wu 2, Zhenzhou Wan 3, Yingxue Li 2, Lulu Zuo 2, Jianru Qin 2,4, Xia Jin 5, Chiyu Zhang 2,
PMCID: PMC7176976  PMID: 32328916

Correction to: Virologica Sinica 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, HCoV-OC43, HCoV-HKU-1, HCoV-NL63 and HCoV-229E). C Cross-reactivity test of the novel SARS-CoV-2 RT-LAMP 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


Articles from Virologica Sinica are provided here courtesy of Wuhan Institute of Virology, Chinese Academy of Sciences

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