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首页> 外文期刊>Journal of computational biology: A journal of computational molecular cell biology >Modified SuperCurve Method for Analysis of Reverse-Phase Protein Array Data
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Modified SuperCurve Method for Analysis of Reverse-Phase Protein Array Data

机译:改进的SuperCurve方法分析反相蛋白质阵列数据

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摘要

Reverse-phase protein arrays (RPPAs) are widely used in biological and biomedical fields of study. One of the most popular analytic methods in RPPA data analysis is the SuperCurve method, which requires estimation of the background fluorescence level. This estimation is usually not accurate and has sample bias and spatial bias. Here, we propose a taking-the-difference method to overcome this problem. Briefly, for each two consecutive RPPA cycles, we subtract the later cycle from the earlier cycle, transforming the m-cycle data into m-1 cycle of data. This removes most of the background fluorescence noise. We then use the m-1 cycle of data to fit a new model accordingly derived from the SuperCurve model. To evaluate our proposed method, we compare the accuracy and precision between our proposed model and the original SuperCurve model by testing them on both real and simulated datasets. For both situations, our modified model shows improved results. The modified SuperCurve method is easy to perform and the taking-the-difference idea is recommended for application to all current methods of RPPA data analysis.
机译:反相蛋白质阵列(RPPA)广泛用于生物和生物医学研究领域。 RPPA数据分析中最流行的分析方法之一是SuperCurve方法,该方法需要估算背景荧光水平。该估计通常不准确,并且具有样本偏差和空间偏差。在这里,我们提出了一种采取差异的方法来克服这个问题。简而言之,对于每两个连续的RPPA周期,我们从较早的周期中减去较晚的周期,从而将m周期数据转换为m-1数据周期。这样可以消除大多数背景荧光噪声。然后,我们使用m-1数据周期来适应从SuperCurve模型衍生而来的新模型。为了评估我们提出的方法,我们通过在真实数据集和模拟数据集上对我们提出的模型和原始SuperCurve模型进行测试,来比较它们的准确性和精度。对于这两种情况,我们的修改模型都显示出改进的结果。修改后的SuperCurve方法易于执行,建议采用差异求和的思想来应用于当前所有RPPA数据分析方法。

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