Fast recursive filters for simulating nonlinear dynamic systems

J. H. van Hateren

Home/Archive/arXiv

arXiv · 0704.1362

Fast recursive filters for simulating nonlinear dynamic systems

J. H. van Hateren

View original source ↗Read source document ↗Export metadata ↓

Abstract

A fast and accurate computational scheme for simulating nonlinear dynamic systems is presented. The scheme assumes that the system can be represented by a combination of components of only two different types: first-order low-pass filters and static nonlinearities. The parameters of these filters and nonlinearities may depend on system variables, and the topology of the system may be complex, including feedback. Several examples taken from neuroscience are given: phototransduction, photopigment bleaching, and spike generation according to the Hodgkin-Huxley equations. The scheme uses two slightly different forms of autoregressive filters, with an implicit delay of zero for feedforward control and an implicit delay of half a sample distance for feedback control. On a fairly complex model of the macaque retinal horizontal cell it computes, for a given level of accuracy, 1-2 orders of magnitude faster than 4th-order Runge-Kutta. The computational scheme has minimal memory requirements, and is also suited for computation on a stream processor, such as a GPU (Graphical Processing Unit).

Explore related subjects

q-bio.QM q-bio.NC

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

J. H. van Hateren. 2007-08-30. Fast recursive filters for simulating nonlinear dynamic systems. https://arxiv.org/abs/0704.1362

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Data-driven multi-agent modelling of calcium interactions in cell culture: PINN vs Regularized Least-squares

Data-driven discovery of dynamics in biological systems allows for better observation and characterization of processes, such as calcium signaling in cell culture. Recent advancements in techniques allow the exploration of previously unattainable insights of dynamical systems, such as the Sparse Identification of Non-Linear Dynamics (SINDy), overcoming the limitations of more classic methodologies. The latter requires some prior knowledge of an effective library of candidate terms, which is not realistic for a real case study. Using inspiration from fields like traffic density estimation and control theory, we propose a methodology for characterization and performance analysis of calcium delivery in a family of cells. In this work, we compare the performance of the Constrained Regularized Least-Squares Method (CRLSM) and Physics-Informed Neural Networks (PINN) for system identification and parameter discovery for governing ordinary differential equations (ODEs). The CRLSM achieves a fairly good parameter estimate and a good data fit when using the learned parameters in the Consensus problem. On the other hand, despite the initial hypothesis, PINNs fail to match the CRLSM performance and, under the current configuration, do not provide fair parameter estimation. However, we have only studied a limited number of PINN architectures, and it is expected that additional hyperparameter tuning, as well as uncertainty quantification, could significantly improve the performance in future works.

q-bio.QM↗

arXiv2026

RNAGenScape: Property-Guided, Optimized Generation of mRNA Sequences with Manifold Langevin Dynamics

Generating property-optimized mRNA sequences is central to applications such as vaccine design and protein replacement therapy, but remains challenging due to limited data, complex sequence-function relationships, and the narrow space of biologically viable sequences. Generative methods that drift away from the data manifold can yield sequences that fail to fold, translate poorly, or are otherwise nonfunctional. We present RNAGenScape, a property-guided manifold Langevin dynamics framework for mRNA sequence generation that operates on a learned manifold of real data. By performing iterative local optimization constrained to this manifold, RNAGenScape preserves favorable computational viability proxies, accesses reliable guidance, and discourages excursions into regions poorly supported by the training data. The framework integrates three components: (1) an autoencoder jointly trained with a property predictor to learn a property-organized latent manifold, (2) a denoising autoencoder that projects updates back onto the manifold, and (3) a property-guided Langevin dynamics procedure that performs optimization along the manifold. Across three real-world mRNA datasets spanning two orders of magnitude in size, RNAGenScape increases median oracle-predicted property gain by up to 267% and success rate by up to 31%, while maintaining good biological viability proxy measures and achieving competitive inference efficiency compared to existing generative approaches.

q-bio.QM↗

arXiv2026

Direct RNA sequence design under codon constraints using expressive tensor-based secondary structure models

Nucleic acid sequence design via codon optimization is a fundamental task with applications across synthetic biology, mRNA therapeutics, and vaccine design. Given a target protein, it is a major open challenge to navigate the combinatorially large design space of codon sequences mapping to its amino acid sequence. Computational approaches generally seek to optimize simple objectives based on the codon sequence, possibly together with more complicated contributions based on secondary structure analysis. In this work, we demonstrate a direct and efficient algorithm to sample sequences from a suitable Boltzmann distribution defined in terms of the codon sequence and a fully detailed secondary structure free energy model, as well as related algorithms for exact computation of statistical quantities such as free energies, base pairing probabilities, and base and codon marginals. These algorithms draw upon a recently developed tensor-based formulation of secondary structure thermodynamics and demonstrate, for the first time, that global sequence design can be accomplished with respect to a highly accurate free energy model. Moreover, the algorithms can leverage any available CPU and GPU resources in parallel for massive computational speedups.

q-bio.QM↗