bennett acceptance ratio
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2020 ◽  
Vol 118 (3) ◽  
pp. 179a
Author(s):  
Ai Shinobu ◽  
Chigusa Kobayashi ◽  
Yasuhiro Matsunaga ◽  
Yuji Sugita

2019 ◽  
Vol 15 (2) ◽  
pp. 799-802 ◽  
Author(s):  
Xinqiang Ding ◽  
Jonah Z. Vilseck ◽  
Charles L. Brooks

2019 ◽  
Vol 16 (0) ◽  
pp. 310-321 ◽  
Author(s):  
Ai Shinobu ◽  
Chigusa Kobayashi ◽  
Yasuhiro Matsunaga ◽  
Yuji Sugita

2018 ◽  
Vol 20 (3) ◽  
pp. 2009-2021 ◽  
Author(s):  
Xiaohui Wang ◽  
Xingzhao Tu ◽  
John Z. H. Zhang ◽  
Zhaoxi Sun

Following the previously proposed equilibrate-state sampling based adaptive sampling regime Optimum Bennett Acceptance Ratio (OBAR), we introduce its nonequilibrium extension, Optimum Crooks’ Equation (OCE) in the current work.


2016 ◽  
Vol 113 (23) ◽  
pp. E3221-E3230 ◽  
Author(s):  
Hao Wu ◽  
Fabian Paul ◽  
Christoph Wehmeyer ◽  
Frank Noé

We introduce the general transition-based reweighting analysis method (TRAM), a statistically optimal approach to integrate both unbiased and biased molecular dynamics simulations, such as umbrella sampling or replica exchange. TRAM estimates a multiensemble Markov model (MEMM) with full thermodynamic and kinetic information at all ensembles. The approach combines the benefits of Markov state models—clustering of high-dimensional spaces and modeling of complex many-state systems—with those of the multistate Bennett acceptance ratio of exploiting biased or high-temperature ensembles to accelerate rare-event sampling. TRAM does not depend on any rate model in addition to the widely used Markov state model approximation, but uses only fundamental relations such as detailed balance and binless reweighting of configurations between ensembles. Previous methods, including the multistate Bennett acceptance ratio, discrete TRAM, and Markov state models are special cases and can be derived from the TRAM equations. TRAM is demonstrated by efficiently computing MEMMs in cases where other estimators break down, including the full thermodynamics and rare-event kinetics from high-dimensional simulation data of an all-atom protein–ligand binding model.


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