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首页> 外文期刊>BMC Bioinformatics >Rational selection of experimental readout and intervention sites for reducing uncertainties in computational model predictions
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Rational selection of experimental readout and intervention sites for reducing uncertainties in computational model predictions

机译:合理选择实验读数和干预位置,以减少计算模型预测中的不确定性

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Background Understanding the dynamics of biological processes can substantially be supported by computational models in the form of nonlinear ordinary differential equations (ODE). Typically, this model class contains many unknown parameters, which are estimated from inadequate and noisy data. Depending on the ODE structure, predictions based on unmeasured states and associated parameters are highly uncertain, even undetermined. For given data, profile likelihood analysis has been proven to be one of the most practically relevant approaches for analyzing the identifiability of an ODE structure, and thus model predictions. In case of highly uncertain or non-identifiable parameters, rational experimental design based on various approaches has shown to significantly reduce parameter uncertainties with minimal amount of effort. Results In this work we illustrate how to use profile likelihood samples for quantifying the individual contribution of parameter uncertainty to prediction uncertainty. For the uncertainty quantification we introduce the profile likelihood sensitivity (PLS) index. Additionally, for the case of several uncertain parameters, we introduce the PLS entropy to quantify individual contributions to the overall prediction uncertainty. We show how to use these two criteria as an experimental design objective for selecting new, informative readouts in combination with intervention site identification. The characteristics of the proposed multi-criterion objective are illustrated with an in silico example. We further illustrate how an existing practically non-identifiable model for the chlorophyll fluorescence induction in a photosynthetic organism, D. salina, can be rendered identifiable by additional experiments with new readouts. Conclusions Having data and profile likelihood samples at hand, the here proposed uncertainty quantification based on prediction samples from the profile likelihood provides a simple way for determining individual contributions of parameter uncertainties to uncertainties in model predictions. The uncertainty quantification of specific model predictions allows identifying regions, where model predictions have to be considered with care. Such uncertain regions can be used for a rational experimental design to render initially highly uncertain model predictions into certainty. Finally, our uncertainty quantification directly accounts for parameter interdependencies and parameter sensitivities of the specific prediction.
机译:背景技术以非线性常微分方程(ODE)的形式建立的计算模型基本上可以支持对生物过程动力学的理解。通常,此模型类包含许多未知参数,这些参数是根据不充分且嘈杂的数据估算的。根据ODE结构,基于未测状态和相关参数的预测是高度不确定的,甚至不确定的。对于给定的数据,轮廓似然分析已被证明是分析ODE结构的可识别性并从而进行模型预测的最实用方法之一。在参数高度不确定或无法确定的情况下,基于各种方法的合理实验设计已显示出以最小的努力即可显着减少参数不确定性。结果在这项工作中,我们说明了如何使用轮廓似然样本来量化参数不确定性对预测不确定性的单独贡献。对于不确定性量化,我们介绍了轮廓似然敏感性(PLS)指数。此外,对于几个不确定参数,我们引入PLS熵来量化对整体预测不确定性的单个贡献。我们展示了如何使用这两个标准作为实验设计目标,以选择新的,信息性强的读数并结合干预部位识别。提出的多标准物镜的特性通过计算机示例说明。我们进一步说明如何通过新的读数进行额外的实验来使光合生物D. salina中的叶绿素荧光诱导的现有实用模型无法识别。结论在手边有数据和轮廓似然样本的情况下,这里提出的基于轮廓似然的预测样本的不确定性量化为确定参数不确定性对模型预测中的不确定性的个体贡献提供了一种简单的方法。通过对特定模型预测的不确定性量化,可以确定需要谨慎考虑模型预测的区域。这样的不确定区域可以用于合理的实验设计,以使最初高度不确定的模型预测变得确定。最后,我们的不确定性量化直接考虑了特定预测的参数相互依赖性和参数敏感性。

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