Zhu Fan, Guan Yuanfang
Department of Computational Medicine and Bioinformatics, Department of Internal Medicine and Department of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Computational Medicine and Bioinformatics, Department of Internal Medicine and Department of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI 48109, USA Department of Computational Medicine and Bioinformatics, Department of Internal Medicine and Department of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI 48109, USA Department of Computational Medicine and Bioinformatics, Department of Internal Medicine and Department of Electrical Engineering and Computer Science, University of Michigan, Ann Arbor, MI 48109, USA.
Bioinformatics. 2014 Oct;30(19):2772-8. doi: 10.1093/bioinformatics/btu382. Epub 2014 Jun 11.
Predicting trajectories of signaling networks under complex perturbations is one of the most valuable, but challenging, tasks in systems biology. Signaling networks are involved in most of the biological pathways, and modeling their dynamics has wide applications including drug design and treatment outcome prediction.
In this paper, we report a novel model for predicting the cell type-specific time course response of signaling proteins under unseen perturbations. This algorithm achieved the top performance in the 2013 8th Dialogue for Reverse Engineering Assessments and Methods (DREAM 8) subchallenge: time course prediction in breast cancer cell lines. We formulate the trajectory prediction problem into a standard regularization problem; the solution becomes solving this discrete ill-posed problem. This algorithm includes three steps: denoising, estimating regression coefficients and modeling trajectories under unseen perturbations. We further validated the accuracy of this method against simulation and experimental data. Furthermore, this method reduces computational time by magnitudes compared to state-of-the-art methods, allowing genome-wide modeling of signaling pathways and time course trajectories to be carried out in a practical time.
Source code is available at http://guanlab.ccmb.med.umich.edu/DREAM/code.html and as supplementary file online.
预测复杂扰动下信号网络的轨迹是系统生物学中最有价值但也最具挑战性的任务之一。信号网络参与了大多数生物途径,对其动力学进行建模具有广泛的应用,包括药物设计和治疗结果预测。
在本文中,我们报告了一种用于预测未见过的扰动下信号蛋白细胞类型特异性时间进程响应的新模型。该算法在2013年第八届逆向工程评估与方法对话(DREAM 8)子挑战:乳腺癌细胞系时间进程预测中取得了最佳性能。我们将轨迹预测问题转化为一个标准的正则化问题;解决方案就是解决这个离散的不适定问题。该算法包括三个步骤:去噪、估计回归系数以及在未见过的扰动下对轨迹进行建模。我们进一步根据模拟和实验数据验证了该方法的准确性。此外,与现有方法相比,该方法将计算时间减少了几个数量级,使得能够在实际时间内对信号通路和时间进程轨迹进行全基因组建模。
源代码可在http://guanlab.ccmb.med.umich.edu/DREAM/code.html获取,并作为在线补充文件提供。