Simultaneous and rapid detection method for measles and rubella using single-tube multiplex real-time quantitative RT-PCR

2019 ◽  
Vol 25 (10) ◽  
pp. 829-831 ◽  
Author(s):  
Nori Yoshioka ◽  
Hideharu Hagiya ◽  
Matsuo Deguchi ◽  
Shigeto Hamaguchi ◽  
Masanori Kagita ◽  
...  
2009 ◽  
Vol 161 (1) ◽  
pp. 70-74 ◽  
Author(s):  
Imadeldin E. Aradaib ◽  
Mohamed E.H. Mohamed ◽  
Mohamed A. Abdalla
Keyword(s):  
Rt Pcr ◽  

The Analyst ◽  
2013 ◽  
Vol 138 (19) ◽  
pp. 5745 ◽  
Author(s):  
Yu Qing Du ◽  
Peng Fei Gao ◽  
Wei Wang ◽  
Ting Ting Wang ◽  
Yong Chang ◽  
...  

2015 ◽  
Vol 14 (4) ◽  
pp. 17496-17504 ◽  
Author(s):  
C.Y. Mu ◽  
A.Y. Wang ◽  
C. Chen ◽  
L. Zhao ◽  
Z. Li
Keyword(s):  
Rt Pcr ◽  

2005 ◽  
Vol 127 (2) ◽  
pp. 148-153 ◽  
Author(s):  
Gwangpyo Ko ◽  
Narayanan Jothikumar ◽  
Vincent R. Hill ◽  
Mark D. Sobsey
Keyword(s):  

BioMedica ◽  
2020 ◽  
Vol 36 (2S) ◽  
pp. 115-120
Author(s):  
Osheen Sajjad ◽  
Aiman Shahzad ◽  
Saqib Mahmood

<p>Coronavirus disease COVID-19, caused by Severe Acute Respiratory Syndrome Corona Virus-2 (SARS-CoV2), is highly contagious and has been a pandemic since March 2020. The SARS-CoV-2 is an enveloped, single-stranded, positive-sense RNA viruswhich spreadsthrough air droplets by sneezing and coughing from affected person. The diagnosis of the COVID-19 remains a challenge to the scientists since the genome of the SARS-CoV-2 was novel and varying. Various studies have reported the validated procedures for sampling and the detection method of SARS-CoV-2. This mini-review provides a brief introduction of the SARS-CoV-2 features and the current knowledge for the recommended COVID19 detection methods including sampling procedures and real time SARS-CoV-2 genome detection.</p>


Author(s):  
Kundan Tandel ◽  
Mahadevan Kumar ◽  
G.S. Bhalla ◽  
S.P.S. Shergill ◽  
Vijaya Swarnim ◽  
...  

2020 ◽  
Vol 21 (16) ◽  
pp. 5674
Author(s):  
Cyril Chik-Yan Yip ◽  
Siddharth Sridhar ◽  
Kit-Hang Leung ◽  
Anthony Chin-Ki Ng ◽  
Kwok-Hung Chan ◽  
...  

Sensitive molecular assays are critical for coronavirus disease 2019 (COVID-19) diagnosis. Here, we designed and evaluated two single-tube nested (STN) real-time RT-PCR assays, targeting SARS-CoV-2 RdRp/Hel and N genes. Both STN assays had a low limit of detection and did not cross react with other human coronaviruses and respiratory viruses. Using 213 initial respiratory specimens from suspected COVID-19 patients, the sensitivity of both the STN COVID-19-RdRp/Hel and the STN COVID-19-N assays was 100% (99/99), while that of the comparator non-nested N assay was 95% (94/99). Among 108 follow-up specimens from confirmed COVID-19 patients who tested negative by the non-nested COVID-19-RdRp/Hel assay, 28 (25.9%) were positive for SARS-CoV-2 by the STN COVID-19-RdRp/Hel or the STN COVID-19-N assay. To evaluate the performance of our novel STN assays in pooled specimens, we created four sample pools, with each pool consisting of one low positive specimen and 49 negative specimens. While the non-nested COVID-19-RdRp/Hel assay was positive in only one of four sample pools (25%), both of the STN assays were positive in two of four samples pools (50%). In conclusion, the STN assays are highly sensitive and specific for SARS-CoV-2 detection. Their boosted sensitivity offers advantages in non-traditional COVID-19 testing algorithms such as saliva screening and pooled sample screening during massive screening.


2020 ◽  
Vol 52 ◽  
pp. 101575
Author(s):  
Min Zheng ◽  
Xiuqin Chen ◽  
Shao Wang ◽  
Jingxiang Wang ◽  
Meiqing Huang ◽  
...  

2020 ◽  
Vol 49 ◽  
pp. 101489 ◽  
Author(s):  
Su Lin ◽  
Shizhong Zhang ◽  
Shao Wang ◽  
Kaichun Xie ◽  
Dandan Jiang ◽  
...  
Keyword(s):  
Rt Pcr ◽  

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