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Kinetics quality assessment for relative quantification by real-time PCR

机译:通过实时PCR进行相对定量的动力学质量评估

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摘要

For proper relative quantification by real-time PCR, compared samples should have similar PCR efficiencies. To test this prerequisite, we developed two quality tests: (i) adjustment of a test for kinetic outlier detection (KOD) to relative quantification; and (ii) comparison of the efficiency variance of test samples with the efficiency variance of samples with highly reproducible quantification. The tests were applied on relative quantification of two genes in 30 sets of 5 replicate samples (same treatment, different animals). Ten low-quality sets and 28 outliers were identified. The low-quality sets showed higher coefficient of variation (cv)% of DNA quantities in replicate experiments than high-quality sets (63% versus 26%; P = 0.001) and contained a higher proportion of outlying quantities (35% versus 5.9%; P = 0.001) when individual samples were detected by adjusted KOD. Outlier detection with adjusted KOD reduced the false detection of outliers by 2/3 compared with the previous, nonadjusted version of KOD (20% versus 5.9%; P = 0.001). We conclude that the presented tests can be used to assign technical reasons to outlying observations.
机译:为了通过实时PCR进行适当的相对定量,比较的样品应具有相似的PCR效率。为了测试此先决条件,我们开发了两个质量测试:(i)将动态离群值检测(KOD)的测试调整为相对定量; (ii)比较测试样品的效率方差与高度可重复定量的样品的效率方差。将测试应用于30组5个重复样品(相同处理,不同动物)中两个基因的相对定量。确定了10个低质量集和28个离群值。低质量组在复制实验中显示的DNA量变异系数(cv)%比高质量组高(63%对26%; P = 0.001),并且包含较高比例的外围量(35%对5.9%) ; P = 0.001)(通过调整的KOD检测单个样品)。与以前的未经调整的KOD版本相比,使用已调整的KOD进行离群值检测可以将离群值的错误检测减少2/3(20%对5.9%; P = 0.001)。我们得出的结论是,提出的测试可用于将技术原因分配给外围观察。

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