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使用经认证的参考材料,通过数字和微滴数字定量PCR测量DNA拷贝数浓度。

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

作者信息

Corbisier Philippe, Pinheiro Leonardo, Mazoua Stéphane, Kortekaas Anne-Marie, Chung Pui Yan Jenny, Gerganova Tsvetelina, Roebben Gert, Emons Hendrik, Emslie Kerry

机构信息

Institute for Reference Materials and Measurements, Joint Research Centre, European Commission, Retieseweg 111, 2440, Geel, Belgium,

出版信息

Anal Bioanal Chem. 2015 Mar;407(7):1831-40. doi: 10.1007/s00216-015-8458-z. Epub 2015 Jan 20.

Abstract

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.

摘要

通过使用BioMark™ HD系统(Fluidigm)的数字PCR(dPCR)对六种认证参考物质(ERM-AD623a-f)的特性进行赋值,每种参考物质均含有每微升100万至10个拷贝的质粒DNA溶液,该赋值已通过使用QX100系统(Bio-Rad)的液滴数字PCR(ddPCR)进行了验证。数字PCR测量拷贝数浓度的关键因素之一是分区体积。因此,我们通过光学显微镜测定了平均液滴体积,发现其平均液滴体积比QuantaSoft软件版本1.3.2.0(Bio-Rad)中用于计算拷贝数浓度的定义参数所使用的液滴体积小8%。这一观察结果解释了为什么使用QuantaSoft软件中预定义的平均液滴体积通过ddPCR估计的拷贝数浓度系统地低于通过dPCR测量的浓度,从而在这两种技术获得的值之间产生了显著偏差。当使用测量得到的0.834 nL液滴体积来估计拷贝数浓度时,差异不再显著。Bio-Rad的新QX200系统和QX100升级版本发布后随之发布的新版本QuantaSoft软件(版本1.6.6.0320)使用0.85 nL的液滴体积作为定义参数来计算拷贝数浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df6/4336415/63d67c7907cd/216_2015_8458_Figa_HTML.jpg

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