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比较实时定量聚合酶链反应分析方法在估计扩增效率的精度、线性和准确性方面的性能。

Comparing real-time quantitative polymerase chain reaction analysis methods for precision, linearity, and accuracy of estimating amplification efficiency.

机构信息

Department of Chemistry, Vanderbilt University, Nashville, TN 37235, USA.

Department of Andrology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Anal Biochem. 2014 Mar 15;449:76-82. doi: 10.1016/j.ab.2013.12.020. Epub 2013 Dec 21.

Abstract

New methods are used to compare seven qPCR analysis methods for their performance in estimating the quantification cycle (Cq) and amplification efficiency (E) for a large test data set (94 samples for each of 4 dilutions) from a recent study. Precision and linearity are assessed using chi-square (χ(2)), which is the minimized quantity in least-squares (LS) fitting, equivalent to the variance in unweighted LS, and commonly used to define statistical efficiency. All methods yield Cqs that vary strongly in precision with the starting concentration N0, requiring weighted LS for proper calibration fitting of Cq vs log(N0). Then χ(2) for cubic calibration fits compares the inherent precision of the Cqs, while increases in χ(2) for quadratic and linear fits show the significance of nonlinearity. Nonlinearity is further manifested in unphysical estimates of E from the same Cq data, results which also challenge a tenet of all qPCR analysis methods - that E is constant throughout the baseline region. Constant-threshold (Ct) methods underperform the other methods when the data vary considerably in scale, as these data do.

摘要

新方法用于比较七种 qPCR 分析方法在估计最近研究中一个大型测试数据集(4 个稀释度的每个样本 94 个)的定量循环(Cq)和扩增效率(E)方面的性能。使用卡方(χ²)评估精度和线性度,这是最小二乘(LS)拟合的最小化量,相当于未加权 LS 的方差,常用于定义统计效率。所有方法都产生了 Cq,其精度随起始浓度 N0 而强烈变化,需要加权 LS 才能正确校准 Cq 与 log(N0)的拟合。然后,用于立方校准拟合的 χ²比较了 Cq 的固有精度,而二次和线性拟合的 χ²增加则显示了非线性的重要性。从相同的 Cq 数据中得出的 E 的非物理估计进一步表明了非线性,这些结果也挑战了所有 qPCR 分析方法的一个原则 - 即在整个基线区域 E 是恒定的。当数据在规模上有很大差异时,如这些数据所示,恒阈(Ct)方法的性能不如其他方法。

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