RT-LAMP functions as using multiple loop primers target the ORF1ab gene and the S gene used for DNA strand displacement activity and then target amplification is used. This method has reported a 100% sensitivity and 100% specificity, and the mean detection time was under 30 minutes. Additionally, RT-LAMP assay was two times faster than qRT-PCR and is storable at room temperature. This permits labs to extend their capacity and process two times more clinical samples. The technique could potentially be used for high-throughput screening purposes.