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Ivan Gilardoni

Publications and source records attributed to Ivan Gilardoni.

4 recordsLinked to original sources

Bayesian Sampling of Structural Ensembles: The Role of Ensemble-Counting Measures

Structural ensemble refinement is widely used to integrate molecular simulations with experimental measurements. While most applications focus on the maximum-a-posteriori (MAP) ensemble, Bayesian sampling of the posterior distribution can provide uncertainty estimates and posterior averages for arbitrary observables. A notable step in this direction was introduced by the Bayesian Energy Landscape Tilting (BELT) framework, where sampling is performed on a family of maximum-entropy ensembles parametrized by Lagrange multipliers. Here, we show that Bayesian sampling in this setting requires an explicit choice of ensemble-counting measure. In particular, the flat measure in Lagrange-multiplier space used in the original BELT formulation leads to a posterior distribution that is formally non-normalizable for finite reference trajectories. We propose the Jeffreys measure as an invariant ensemble-counting prescription, restoring normalizability in the finite-sample situations considered here, and providing a consistent definition of posterior averages. Using both an analytically tractable Gaussian model and maximum-entropy refinement of RNA oligomer simulations, we compare different ensemble-counting measures and show that they can significantly affect Bayesian estimates. The resulting methodology has been implemented in the \texttt{MDRefine} software package.

physics.chem-ph

MDRefine: a Python package for refining Molecular Dynamics trajectories with experimental data

Molecular dynamics (MD) simulations play a crucial role in resolving the underlying conformational dynamics of molecular systems. However, their capability to correctly reproduce and predict dynamics in agreement with experiments is limited by the accuracy of the force-field model. This capability can be improved by refining the structural ensembles or the force-field parameters. Furthermore, discrepancies with experimental data can be due to imprecise forward models, namely, functions mapping simulated structures to experimental observables. Here, we introduce MDRefine, a Python package aimed at implementing the refinement of the ensemble, the force-field and/or the forward model by comparing MD-generated trajectories with experimental data. The software consists of several tools that can be employed separately from each other or combined together in different ways, providing a seamless interpolation between these three different types of refinement. We use some benchmark cases to show that the combined approach is superior to separately applied refinements. Source code, documentation and examples are freely available at https://pypi.org/project/MDRefine and https://github.com/bussilab/MDRefine.

physics.chem-ph

Boosting ensemble refinement with transferable force field corrections: synergistic optimization for molecular simulations

A novel method combining the ensemble refinement by maximum entropy principle and the force field fitting approach is presented. Its formulation allows to continuously interpolate in between these two methods, which can thus be interpreted as two limiting cases. A cross-validation procedure enables to correctly assess the relative weight of both of them, distinguishing scenarios where the combined approach is meaningful from those in which either ensemble refinement or force field fitting separately prevails. The efficacy of their combination is examined for a realistic case study of RNA oligomers. Within the new scheme, molecular dynamics simulations are integrated with experimental data provided by nuclear-magnetic-resonance measures. We show that force field corrections are in general superior when applied to the appropriate force field terms, but are automatically discarded by the method when applied to inappropriate force field terms.

physics.chem-ph

A real-space many-body marker for correlated ${\mathbb Z}_2$ topological insulators

Taking the clue from the modern theory of polarization [R. Resta, Rev. Mod. Phys. {\bf 66}, 899 (1994)], we identify an operator to distinguish between ${\mathbb Z}_2$-even (trivial) and ${\mathbb Z}_2$-odd (topological) insulators in two spatial dimensions. Its definition extends the position operator [R. Resta and S. Sorella, Phys. Rev. Lett. {\bf 82}, 370 (1999)], which was introduced in one-dimensional systems. We first show a few examples of non-interacting models, where single-particle wave functions are defined and allow for a direct comparison with standard techniques on large system sizes. Then, we illustrate its applicability for an interacting model on a small cluster, where exact diagonalizations are available. Its formulation in the Fock space allows a direct computation of expectation values over the ground-state wave function (or any approximation of it), thus allowing us to investigate generic interacting systems, such as strongly-correlated topological insulators.

cond-mat.str-el