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A black-box re-weighting analysis can correct flawed simulation data

机译:黑盒重新加权分析可以纠正有缺陷的模拟数据

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摘要

There is a great need for improved statistical sampling in a range of physical, chemical, and biological systems. Even simulations based on correct algorithms suffer from statistical error, which can be substantial or even dominant when slow processes are involved. Further, in key biomolecular applications, such as the determination of protein structures from NMR data, non-Boltzmann-distributed ensembles are generated. We therefore have developed the “black-box” strategy for reweighting a set of configurations generated by arbitrary means to produce an ensemble distributed according to any target distribution. In contrast to previous algorithmic efforts, the black-box approach exploits the configuration-space density observed in a simulation, rather than assuming a desired distribution has been generated. Successful implementations of the strategy, which reduce both statistical error and bias, are developed for a one-dimensional system, and a 50-atom peptide, for which the correct 250-to-1 population ratio is recovered from a heavily biased ensemble.
机译:迫切需要在一系列物理,化学和生物系统中改进统计抽样。甚至基于正确算法的仿真也会遭受统计误差,当涉及到缓慢的过程时,统计误差可能很大,甚至占支配地位。此外,在关键的生物分子应用中,例如从NMR数据确定蛋白质结构,会生成非玻耳兹曼分布的集合体。因此,我们开发了“黑匣子”策略,用于对通过任意方式生成的一组配置进行加权,以根据任何目标分布生成整体分布。与以前的算法工作相比,黑盒方法利用了在仿真中观察到的配置空间密度,而不是假设已经生成了所需的分布。针对一维系统和50原子肽开发了可同时减少统计误差和偏倚的策略成功实施方案,可从严重偏向的整体中获得正确的250:1人口比例。

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