Search arXiv⌕ Search

arXiv subjects

Vincent D. Zaballa

Publications and source records attributed to Vincent D. Zaballa.

7 recordsLinked to original sources

Scalable Diffusion SBI for Compositional Inference under Simulator Misspecification

Simulation-based inference is challenging when many heterogeneous observations must be composed, hierarchical latent structure must be preserved, and the simulator is misspecified relative to observed data. We develop sampling and fine-tuning methods for diffusion-based inference in design-conditional settings, where the same simulator is queried across different experimental conditions $ξ$. We extend compositional score-based inference with a continuous-time diffusion coefficient that accounts for the number of observations, avoiding Jacobian and auxiliary-covariance corrections. We introduce Hierarchical Blockwise Diffusion Sampling (HBDS), which infers shared parameters and group-specific latent states using a single pretrained model, with the hierarchy specified only at sampling time. Together, these methods support variable observation sets and groupings without retraining. To address misspecification, we introduce path-regularized fine-tuning that adapts the learned likelihood to observations and transfers corrections to posterior inference. Using Girsanov's theorem, we quantify path divergence between pretrained and fine-tuned models across experimental designs and interpret it alongside predictive errors to distinguish candidate misspecification correction from unnecessary adaptation. We evaluate compositional sampling on exact-score Gaussian and Simple Likelihood, Complex Posterior benchmarks, HBDS with analytic and learned scores on a controlled hierarchical model, and fine-tuning and localization on a separate analytic model with known design-dependent discrepancy. Finally, we apply the framework to 940 measurements across four cell lines in a mechanistic Bone Morphogenetic Protein signaling model, where fine-tuning improves posterior-predictive accuracy relative to the pretrained model and shifts posterior marginals toward the least-squares reference while retaining spread.

cs.LG↗

Optimizing Likelihoods via Mutual Information: Bridging Simulation-Based Inference and Bayesian Optimal Experimental Design

Simulation-based inference (SBI) is a method to perform inference on a variety of complex scientific models with challenging inference (inverse) problems. Bayesian Optimal Experimental Design (BOED) aims to efficiently use experimental resources to make better inferences. Various stochastic gradient-based BOED methods have been proposed as an alternative to Bayesian optimization and other experimental design heuristics to maximize information gain from an experiment. We demonstrate a link via mutual information bounds between SBI and stochastic gradient-based variational inference methods that permits BOED to be used in SBI applications as SBI-BOED. This link allows simultaneous optimization of experimental designs and optimization of amortized inference functions. We evaluate the pitfalls of naive design optimization using this method in a standard SBI task and demonstrate the utility of a well-chosen design distribution in BOED. We compare this approach on SBI-based models in real-world simulators in epidemiology and biology, showing notable improvements in inference.

stat.ML↗

Systems-Structure-Based Drug Design

Recent advances in generative deep learning have transformed small molecule design, but most methods lack biological systems context, focusing narrowly on specific protein pockets. We introduce a non-differentiable diffusion guidance method that integrates systems biology models, enhancing small molecule generation with pathway context. Using the Bone Morphogenetic Protein (BMP) pathway, we generate small molecules specific to one protein over competing proteins. This method enhances the precision and efficiency of small molecule drug discovery by incorporating systems biology insights into generative models.

q-bio.BM↗

Reducing Uncertainty Through Mutual Information in Structural and Systems Biology

Systems biology models are useful models of complex biological systems that may require a large amount of experimental data to fit each model's parameters or to approximate a likelihood function. These models range from a few to thousands of parameters depending on the complexity of the biological system modeled, potentially making the task of fitting parameters to the model difficult - especially when new experimental data cannot be gathered. We demonstrate a method that uses structural biology predictions to augment systems biology models to improve systems biology models' predictions without having to gather more experimental data. Additionally, we show how systems biology models' predictions can help evaluate novel structural biology hypotheses, which may also be expensive or infeasible to validate.

q-bio.QM↗

Approximation of Intractable Likelihood Functions in Systems Biology via Normalizing Flows

Systems biology relies on mathematical models that often involve complex and intractable likelihood functions, posing challenges for efficient inference and model selection. Generative models, such as normalizing flows, have shown remarkable ability in approximating complex distributions in various domains. However, their application in systems biology for approximating intractable likelihood functions remains unexplored. Here, we elucidate a framework for leveraging normalizing flows to approximate complex likelihood functions inherent to systems biology models. By using normalizing flows in the Simulation-based inference setting, we demonstrate a method that not only approximates a likelihood function but also allows for model inference in the model selection setting. We showcase the effectiveness of this approach on real-world systems biology problems, providing practical guidance for implementation and highlighting its advantages over traditional computational methods.

q-bio.QM↗

Stochastic Gradient Bayesian Optimal Experimental Designs for Simulation-based Inference

Simulation-based inference (SBI) methods tackle complex scientific models with challenging inverse problems. However, SBI models often face a significant hurdle due to their non-differentiable nature, which hampers the use of gradient-based optimization techniques. Bayesian Optimal Experimental Design (BOED) is a powerful approach that aims to make the most efficient use of experimental resources for improved inferences. While stochastic gradient BOED methods have shown promising results in high-dimensional design problems, they have mostly neglected the integration of BOED with SBI due to the difficult non-differentiable property of many SBI simulators. In this work, we establish a crucial connection between ratio-based SBI inference algorithms and stochastic gradient-based variational inference by leveraging mutual information bounds. This connection allows us to extend BOED to SBI applications, enabling the simultaneous optimization of experimental designs and amortized inference functions. We demonstrate our approach on a simple linear model and offer implementation details for practitioners.

cs.LG↗

An Optimal Likelihood Free Method for Biological Model Selection

Systems biology seeks to create math models of biological systems to reduce inherent biological complexity and provide predictions for applications such as therapeutic development. However, it remains a challenge to determine which math model is correct and how to arrive optimally at the answer. We present an algorithm for automated biological model selection using mathematical models of systems biology and likelihood free inference methods. Our algorithm shows improved performance in arriving at correct models without a priori information over conventional heuristics used in experimental biology and random search. This method shows promise to accelerate biological basic science and drug discovery.

q-bio.QM↗