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Automatic error control during forward flux sampling of rare events in master equation models

机译:母型方程模型稀有事件前向通量采样过程中的自动错误控制

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Enhanced sampling methods, such as forward flux sampling (FFS), have great capacity for accelerating stochastic simulations of nonequilibrium biochemical systems involving rare events. However, the description of the tradeoffs between simulation efficiency and error in FFS remains incomplete. We present a novel and mathematically rigorous analysis of the errors in FFS that, for the first time, covers the contribution of every phase of the simulation. We derive a closed form expression for the optimally efficient count of samples to take in each FFS phase in terms of a fixed constraint on sampling error. We introduce a new method, forward flux pilot sampling (FFPilot), that is designed to take full advantage of our optimizing equation without prior information or assumptions about the phase weights and costs along the transition path. In simulations of both single and multidimensional gene regulatory networks, FFPilot is able to completely control sampling error. We then discuss how memory effects can introduce additional error when relaxation along the transition path is slow. This extra error can be traced to correlations between the FFS phases and can be controlled by monitoring the covariance between them. Finally, we show that, in sets of simulations with matched error, FFPilot is on the order of tens-to-hundreds of times faster than direct sampling and noticeably more efficient than previous FFS methods.
机译:增强的采样方法,如前向通量采样(FFS),具有很大的能力,可加速涉及罕见事件的非纤维化生物化学系统的随机仿真。但是,模拟效率与FF中误差之间的权衡描述仍然不完整。我们提出了一种小说和数学上严格分析了FFS中的错误,这是第一次涵盖模拟的每个阶段的贡献。我们派生了一个封闭的表达式表达式,以获得对采样误差的固定约束的每个FFS相位进行最佳有效的样本计数。我们介绍了一种新的方法,正向助焊试验采样(FFPilot),该方法旨在充分利用我们的优化方程,而无需现有信息或关于阶段权重和沿着转换路径的成本的假设。在单一和多维基因监管网络的模拟中,FFPilot能够完全控制采样误差。然后,我们讨论在沿着过渡路径放松时,记忆效果如何引入额外的错误。可以将该额外错误追溯到FFS阶段之间的相关性,并且可以通过监视它们之间的协方差来控制。最后,我们表明,在具有匹配错误的模拟集合中,FFPilot比直接采样快,比前一个FFS方法更快的数百次。

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