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Development of a sampling-based global sensitivity analysis workflow for multiscale computational cancer models

机译:开发用于多尺度计算癌症模型的采样的全局敏感性分析工作流程

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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 study, the authors 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; they then exemplify this workflow using a two-dimensional multiscale lung cancer model. By accounting for all parameter rankings produced by multiple GSA methods, a summarised 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 extracellular signal-regulated kinase, a downstream molecule of the epidermal growth factor receptor signalling pathway, has the most important impact on regulating both the tumour volume and expansion rate in the algorithm used.
机译:在在MultiScale“在硅”癌症模型中对多尺度`进行全球敏感性分析(GSA)时,研究人员面临的两个挑战。首先是增加的计算强度,因为多尺度癌症模型通常需要更长时间地运行而不是特定于比例的模型。第二个问题是缺乏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序列。因此,作者因此提出了一种由三个阶段组成的基于采样的GSA工作流 - 通过整合Monte Carlo和重采样方法,通过重复使用方差分析来分析,分析和分析 - 分析。然后,它们使用二维多尺度肺癌模型举例说明该工作流程。通过对多个GSA方法产生的所有参数排名进行计入,基于每个输入参数的排名的加权平均值在工作流结束时创建总结排名。对于此处研究的癌症模型,该分析表明,细胞外信号调节激酶是表皮生长因子受体信号传导途径的下游分子对调节算法中使用的算法中的肿瘤体积和膨胀率最重要的影响。

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