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与QIAamp Mini试剂盒相比,对临床样本中自动化NucliSens easyMAG核酸提取平台的性能评估。

Performance evaluation of the automated NucliSens easyMAG nucleic acid extraction platform in comparison with QIAamp Mini kit from clinical specimens.

作者信息

Perandin Francesca, Pollara Patrizia C, Gargiulo Franco, Bonfanti Carlo, Manca Nino

机构信息

Department of Experimental and Applied Medicine, University of Brescia, Italy.

出版信息

Diagn Microbiol Infect Dis. 2009 Jun;64(2):158-65. doi: 10.1016/j.diagmicrobio.2009.02.013.

Abstract

The performance of the NucliSens easyMAG platform for the extraction of nucleic acid from different clinical specimens was compared with a manual procedure. A total of 308 specimens were analyzed: 209 plasma samples collected for virus detection and quantification of cytomegalovirus (CMV) and Epstein-Barr virus (EBV) (n = 70), and 29 for HIV genotyping for drug resistance. Linearity of extraction was tested on dilution series of CMV and EBV; the correlation coefficient (R(2)) for standard curves based on repeated extraction runs was 0.99 for CMV and EBV. Inter- and intrarun variability was in accordance with previous studies, and the correlation between automated and manual extraction was very high. The concordant results were 95.7% for CMV and 100% for EBV. The results of sequence analysis for HIV drug resistance showed a concordance in 24 of 29 specimens. The NucliSens easyMAG is extremely easy to perform, is automated, and resulted in a strong reduction of hands-on time compared with manual protocol.

摘要

将NucliSens easyMAG平台从不同临床标本中提取核酸的性能与手工操作方法进行了比较。共分析了308份标本:209份用于病毒检测及巨细胞病毒(CMV)和EB病毒(EBV)定量的血浆样本(n = 70),以及29份用于HIV耐药性基因分型的样本。在CMV和EBV的稀释系列上测试了提取的线性;基于重复提取运行的标准曲线的相关系数(R²)对于CMV和EBV均为0.99。批间和批内变异性与先前研究一致,并且自动提取和手工提取之间的相关性非常高。CMV的一致结果为95.7%,EBV的一致结果为100%。HIV耐药性的序列分析结果显示,29份标本中有24份结果一致。NucliSens easyMAG操作极其简便,是自动化的,与手工操作方案相比,大大减少了实际操作时间。

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