scholarly journals Plasmon-enhanced fluorescence imaging with silicon-based silver chips for protein and nucleic acid assay

2017 ◽  
Vol 955 ◽  
pp. 98-107 ◽  
Author(s):  
Bing Yuan ◽  
Xiangxu Jiang ◽  
Chu Yao ◽  
Meimei Bao ◽  
Jiaojiao Liu ◽  
...  
2021 ◽  
Vol 13 (2) ◽  
pp. 3098-3108
Author(s):  
Yunho Choi ◽  
Younseong Song ◽  
Yong Tae Kim ◽  
Seok Jae Lee ◽  
Kyoung G. Lee ◽  
...  

Author(s):  
Zhi-Hong Xu ◽  
Hang Gao ◽  
Nan Zhang ◽  
Wei Zhao ◽  
Yi-Xiang Cheng ◽  
...  

Nanophotonics ◽  
2017 ◽  
Vol 6 (2) ◽  
pp. 502 ◽  
Author(s):  
Jun Dong ◽  
Zhenglong Zhang ◽  
Hairong Zheng ◽  
Mengtao Sun

Nanoscale ◽  
2016 ◽  
Vol 8 (42) ◽  
pp. 18150-18160 ◽  
Author(s):  
Ying You ◽  
Quanwei Song ◽  
Le Wang ◽  
Caixia Niu ◽  
Na Na ◽  
...  

2015 ◽  
Vol 119 (33) ◽  
pp. 19350-19358 ◽  
Author(s):  
Bing Fu ◽  
Jessica D. Flynn ◽  
Benjamin P. Isaacoff ◽  
David J. Rowland ◽  
Julie S. Biteen

2014 ◽  
Vol 104 (10) ◽  
pp. 1125-1129 ◽  
Author(s):  
A. H. Stobbe ◽  
W. L. Schneider ◽  
P. R. Hoyt ◽  
U. Melcher

Next generation sequencing (NGS) is not used commonly in diagnostics, in part due to the large amount of time and computational power needed to identify the taxonomic origin of each sequence in a NGS data set. By using the unassembled NGS data sets as the target for searches, pathogen-specific sequences, termed e-probes, could be used as queries to enable detection of specific viruses or organisms in plant sample metagenomes. This method, designated e-probe diagnostic nucleic acid assay, first tested with mock sequence databases, was tested with NGS data sets generated from plants infected with a DNA (Bean golden yellow mosaic virus, BGYMV) or an RNA (Plum pox virus, PPV) virus. In addition, the ability to detect and differentiate among strains of a single virus species, PPV, was examined by using probe sets that were specific to strains. The use of probe sets for multiple viruses determined that one sample was dually infected with BGYMV and Bean golden mosaic virus.


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