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Rapid Sanger sequencing of the 16S rRNA gene for identification of some common pathogens.

Conventional Sanger sequencing remains time-consuming and laborious. In this study, we developed a rapid improved sequencing protocol of 16S rRNA for pathogens identification by using a new combination of SYBR Green I real-time PCR and Sanger sequencing with FTA® cards. To compare the sequencing qua...

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Hlavní autoři: Linxiang Chen, Ying Cai, Guangbiao Zhou, Xiaojun Shi, Jianhui Su, Guanwu Chen, Kun Lin
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science (PLoS) 2014-01-01
Edice:PLoS ONE
On-line přístup:http://europepmc.org/articles/PMC3925228?pdf=render
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