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Development of a Sampling-Based Global Sensitivity Analysis Workflow for Multiscale Computational Cancer Models

机译:多样本计算癌症模型的基于采样的全局敏感性分析工作流的开发

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摘要

There are two challenges that researchers face when performing global sensitivity analysis (GSA) on multiscale in silico cancer models. The first is increased computational intensity, since a multiscale cancer model generally takes longer to run than does a scale-specific model. The second problem is the lack of a best GSA method that fits all types of models, which implies that multiple methods and their sequence need to be taken into account. In this article, we therefore propose a sampling-based GSA workflow consisting of three phases – pre-analysis, analysis, and post-analysis – by integrating Monte Carlo and resampling methods with the repeated use of analysis of variance (ANOVA); we then exemplify this workflow using a two-dimensional multiscale lung cancer model. By accounting for all parameter rankings produced by multiple GSA methods, a summarized ranking is created at the end of the workflow based on the weighted mean of the rankings for each input parameter. For the cancer model investigated here, this analysis reveals that ERK, a downstream molecule of the EGFR signaling pathway, has the most important impact on regulating both the tumor volume and expansion rate in the algorithm used.
机译:在多尺度计算机模拟癌症模型上进行全局敏感性分析(GSA)时,研究人员面临两个挑战。首先是计算强度的提高,因为多尺度癌症模型的运行时间通常比特定规模的模型要长。第二个问题是缺少适合所有类型模型的最佳GSA方法,这意味着需要考虑多种方法及其顺序。因此,在本文中,我们通过结合蒙特卡洛方法和重采样方法以及重复使用方差分析(ANOVA),提出了一个基于抽样的GSA工作流程,包括三个阶段-前分析,分析和后分析。然后,我们使用二维多尺度肺癌模型来举例说明此工作流程。通过考虑由多种GSA方法产生的所有参数排名,在工作流末尾基于每个输入参数的排名的加权平均值创建汇总排名。对于此处研究的癌症模型,该分析表明,在所使用的算法中,ERK是EGFR信号传导途径的下游分子,对调节肿瘤体积和扩展率具有最重要的影响。

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