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DNA copy number concentration measured by digital and droplet digital quantitative PCR using certified reference materials

机译:使用认证的参考物质通过数字和液滴数字定量PCR测量的DNA拷贝数浓度

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摘要

The value assignment for properties of six certified reference materials (ERM-AD623a–f), each containing a plasmid DNA solution ranging from 1 million to 10 copies per μL, by using digital PCR (dPCR) with the BioMark™ HD System (Fluidigm) has been verified by applying droplet digital PCR (ddPCR) using the QX100 system (Bio-Rad). One of the critical factors in the measurement of copy number concentrations by digital PCR is the partition volume. Therefore, we determined the average droplet volume by optical microscopy, revealing an average droplet volume that is 8 % smaller than the droplet volume used as the defined parameter in the QuantaSoft software version 1.3.2.0 (Bio-Rad) to calculate the copy number concentration. This observation explains why copy number concentrations estimated with ddPCR and using an average droplet volume predefined in the QuantaSoft software were systematically lower than those measured by dPCR, creating a significant bias between the values obtained by these two techniques. The difference was not significant anymore when the measured droplet volume of 0.834 nL was used to estimate copy number concentrations. A new version of QuantaSoft software (version 1.6.6.0320), which has since been released with Bio-Rad’s new QX200 systems and QX100 upgrades, uses a droplet volume of 0.85 nL as a defined parameter to calculate copy number concentration.>Graphical AbstractMonolayer of droplets generated by the droplet generator and observed under an optical microscope
机译:通过使用带有BioMark™HD系统(Fluidigm)的数字PCR(dPCR),对六种经过认证的参考材料(ERM-AD623a-f)的属性进行值分配,每种参考材料均包含每μL百万至10拷贝的质粒DNA溶液已通过使用QX100系统(Bio-Rad)的液滴数字PCR(ddPCR)进行了验证。通过数字PCR测量拷贝数浓度的关键因素之一是分配体积。因此,我们通过光学显微镜确定了平均液滴体积,发现平均液滴体积比QuantaSoft软件版本1.3.2.0(Bio-Rad)中用作定义参数的液滴体积小8%,以计算拷贝数浓度。该观察结果解释了为什么用ddPCR估算并使用QuantaSoft软件中预定义的平均液滴体积估算的拷贝数浓度总体上低于dPCR所测量的拷贝数浓度,从而在这两种技术获得的值之间产生显着偏差。当使用测得的液滴体积为0.834 nL来估计拷贝数浓度时,差异不再显着。自Bio-Rad的新QX200系统和QX100升级以来发布的新版QuantaSoft软件(版本1.6.6.0320)使用0.85 nL的墨滴量作为定义的参数来计算拷贝数浓度。图ft0-> <!-fig @ position =“ anchor” mode = article f4-> <!-fig mode =“ anchored” f5-> >图形摘要<!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题a7->由液滴产生器产生并在光学显微镜下观察到的单层液滴

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