首页> 美国卫生研究院文献>PLoS Computational Biology >FAMoS: A Flexible and dynamic Algorithm for Model Selection to analyse complex systems dynamics
【2h】

FAMoS: A Flexible and dynamic Algorithm for Model Selection to analyse complex systems dynamics

机译:FAMoS:灵活而动态的模型选择算法可分析复杂的系统动力学

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Most biological systems are difficult to analyse due to a multitude of interacting components and the concomitant lack of information about the essential dynamics. Finding appropriate models that provide a systematic description of such biological systems and that help to identify their relevant factors and processes can be challenging given the sheer number of possibilities. Model selection algorithms that evaluate the performance of a multitude of different models against experimental data provide a useful tool to identify appropriate model structures. However, many algorithms addressing the analysis of complex dynamical systems, as they are often used in biology, compare a preselected number of models or rely on exhaustive searches of the total model space which might be unfeasible dependent on the number of possibilities. Therefore, we developed an algorithm that is able to perform model selection on complex systems and searches large model spaces in a dynamical way. Our algorithm includes local and newly developed non-local search methods that can prevent the algorithm from ending up in local minima of the model space by accounting for structurally similar processes. We tested and validated the algorithm based on simulated data and showed its flexibility for handling different model structures. We also used the algorithm to analyse experimental data on the cell proliferation dynamics of CD4+ and CD8+ T cells that were cultured under different conditions. Our analyses indicated dynamical changes within the proliferation potential of cells that was reduced within tissue-like 3D ex vivo cultures compared to suspension. Due to the flexibility in handling various model structures, the algorithm is applicable to a large variety of different biological problems and represents a useful tool for the data-oriented evaluation of complex model spaces.
机译:由于许多相互作用的成分以及随之而来的关于基本动力学的信息的缺乏,大多数生物系统难以分析。鉴于存在的可能性之多,寻找合适的模型来提供对此类生物系统的系统描述并有助于识别其相关因素和过程可能具有挑战性。根据实验数据评估多种不同模型的性能的模型选择算法提供了一种有用的工具,可以识别适当的模型结构。但是,许多解决复杂动力学系统分析的算法(通常在生物学中使用)比较模型的预选数量,或者依赖于对整个模型空间的详尽搜索,而这可能取决于可能性的数量。因此,我们开发了一种能够在复杂系统上执行模型选择并以动态方式搜索大型模型空间的算法。我们的算法包括本地和新近开发的非本地搜索方法,这些方法可以通过考虑结构上相似的过程来防止算法最终出现在模型空间的局部最小值中。我们基于模拟数据对算法进行了测试和验证,并显示了它在处理不同模型结构方面的灵活性。我们还使用该算法分析了在不同条件下培养的CD4 + 和CD8 + T细胞的细胞增殖动力学的实验数据。我们的分析表明,与悬浮液相比,组织样3D离体培养物中细胞增殖潜能的动态变化有所降低。由于处理各种模型结构的灵活性,该算法适用于各种不同的生物学问题,并且代表了一种用于对复杂模型空间进行面向数据的评估的有用工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号