Comment on “MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21”

2013 ◽  
Vol 33 (4) ◽  
pp. 403-403 ◽  
Author(s):  
Han Qin ◽  
Michael Bonifacio ◽  
Steven McArthur ◽  
Andrew McLennan ◽  
Tom Boogert ◽  
...  
2012 ◽  
Vol 32 (10) ◽  
pp. 996-1001 ◽  
Author(s):  
Evdokia Tsaliki ◽  
Elisavet A. Papageorgiou ◽  
Christiana Spyrou ◽  
George Koumbaris ◽  
Elena Kypri ◽  
...  

2003 ◽  
Vol 44 (2) ◽  
pp. 181 ◽  
Author(s):  
Young Ho Yang ◽  
Sung Hoon Kim ◽  
Eun Suk Yang ◽  
Sei Kwang Kim ◽  
In Kyu Kim ◽  
...  

Epigenetics ◽  
2014 ◽  
Vol 9 (10) ◽  
pp. 1360-1365 ◽  
Author(s):  
John K Wiencke ◽  
Paige M Bracci ◽  
George Hsuang ◽  
Shichun Zheng ◽  
Helen Hansen ◽  
...  

2021 ◽  
Vol 9 (4) ◽  
pp. 765
Author(s):  
Janika Wolff ◽  
Martin Beer ◽  
Bernd Hoffmann

Outbreaks of the three capripox virus species, namely lumpy skin disease virus, sheeppox virus, and goatpox virus, severely affect animal health and both national and international economies. Therefore, the World Organization for Animal Health (OIE) classified them as notifiable diseases. Until now, discrimination of capripox virus species was possible by using different conventional PCR protocols. However, more sophisticated probe-based real-time qPCR systems addressing this issue are, to our knowledge, still missing. In the present study, we developed several duplex qPCR assays consisting of different types of fluorescence-labelled probes that are highly sensitive and show a high analytical specificity. Finally, our assays were combined with already published diagnostic methods to a diagnostic workflow that enables time-saving, reliable, and robust detection, differentiation, and characterization of capripox virus isolates.


1992 ◽  
Vol 12 (6) ◽  
pp. 547-548 ◽  
Author(s):  
Y.-M. D. Lo ◽  
J. S. Wainscoat ◽  
K. A. Fleming

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