数字聚合酶链反应
实时聚合酶链反应
连续稀释
乙型肝炎病毒
病毒学
DNA
生物
多路复用
分子生物学
计算生物学
聚合酶链反应
病毒
医学
生物信息学
遗传学
病理
基因
替代医学
作者
Hui Tang,Qingchun Cai,Hu Li,Peng Hu
标识
DOI:10.1080/09168451.2016.1196576
摘要
Quantitative real-time PCR (qPCR) has been widely implemented for clinical hepatitis B viral load testing, but a lack of standardization and relatively poor precision hinder its usefulness. Droplet digital PCR (ddPCR) is a promising tool that offers high precision and direct quantification. In this study, we compared the ddPCR QX100 platform by Bio-Rad with the CFX384 Touch Real-Time PCR Detection System (Bio-Rad, USA) to detect serial plasmid DNA dilutions of known concentrations as well as HBV DNA extracted from patient serum samples. Both methods showed a high degree of linearity and quantitative correlation. However, ddPCR assays generated more reproducible results and detected lower copy numbers than qPCR assays. Patient sample quantifications by ddPCR and qPCR were highly agreeable based on the Bland-Altman analysis. Collectively, our findings demonstrate that ddPCR offers improved analytical sensitivity and specificity for HBV measurements and is suitable for clinical HBV detection.
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