Steiert Bernhard, Timmer Jens, Kreutz Clemens
Institute of Physics.
Institute of Physics BIOSS Centre for Biological Signalling Studies Freiburg Center for Systems Biology (ZBSA), University of Freiburg, Germany.
Bioinformatics. 2016 Sep 1;32(17):i718-i726. doi: 10.1093/bioinformatics/btw461.
A major goal of drug development is to selectively target certain cell types. Cellular decisions influenced by drugs are often dependent on the dynamic processing of information. Selective responses can be achieved by differences between the involved cell types at levels of receptor, signaling, gene regulation or further downstream. Therefore, a systematic approach to detect and quantify cell type-specific parameters in dynamical systems becomes necessary.
Here, we demonstrate that a combination of nonlinear modeling with L1 regularization is capable of detecting cell type-specific parameters. To adapt the least-squares numerical optimization routine to L1 regularization, sub-gradient strategies as well as truncation of proposed optimization steps were implemented. Likelihood-ratio tests were used to determine the optimal regularization strength resulting in a sparse solution in terms of a minimal number of cell type-specific parameters that is in agreement with the data. By applying our implementation to a realistic dynamical benchmark model of the DREAM6 challenge we were able to recover parameter differences with an accuracy of 78%. Within the subset of detected differences, 91% were in agreement with their true value. Furthermore, we found that the results could be improved using the profile likelihood. In conclusion, the approach constitutes a general method to infer an overarching model with a minimum number of individual parameters for the particular models.
A MATLAB implementation is provided within the freely available, open-source modeling environment Data2Dynamics. Source code for all examples is provided online at http://www.data2dynamics.org/
药物研发的一个主要目标是选择性地靶向某些细胞类型。受药物影响的细胞决策通常依赖于信息的动态处理。通过相关细胞类型在受体、信号传导、基因调控或更下游水平的差异,可以实现选择性反应。因此,有必要采用一种系统的方法来检测和量化动态系统中细胞类型特异性参数。
在此,我们证明了非线性建模与L1正则化相结合能够检测细胞类型特异性参数。为了使最小二乘数值优化程序适应L1正则化,实施了次梯度策略以及对提议的优化步骤进行截断。似然比检验用于确定最优正则化强度,从而在与数据一致的最少细胞类型特异性参数数量方面得到一个稀疏解。通过将我们的实现应用于DREAM6挑战赛的一个实际动态基准模型,我们能够以78%的准确率恢复参数差异。在检测到的差异子集中,91%与它们的真实值一致。此外,我们发现使用轮廓似然可以改进结果。总之,该方法构成了一种通用方法,可为特定模型推断出具有最少单个参数的总体模型。
在免费的开源建模环境Data2Dynamics中提供了MATLAB实现。所有示例的源代码可在http://www.data2dynamics.org/在线获取。