Paper List
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Macroscopic Dominance from Microscopic Extremes: Symmetry Breaking in Spatial Competition
This paper addresses the fundamental question of how microscopic stochastic advantages in spatial exploration translate into macroscopic resource domi...
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Linear Readout of Neural Manifolds with Continuous Variables
This paper addresses the core challenge of quantifying how the geometric structure of high-dimensional neural population activity (neural manifolds) d...
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Theory of Cell Body Lensing and Phototaxis Sign Reversal in “Eyeless” Mutants of Chlamydomonas
This paper solves the core puzzle of how eyeless mutants of Chlamydomonas exhibit reversed phototaxis by quantitatively modeling the competition betwe...
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Cross-Species Transfer Learning for Electrophysiology-to-Transcriptomics Mapping in Cortical GABAergic Interneurons
This paper addresses the challenge of predicting transcriptomic identity from electrophysiological recordings in human cortical interneurons, where li...
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Uncovering statistical structure in large-scale neural activity with Restricted Boltzmann Machines
This paper addresses the core challenge of modeling large-scale neural population activity (1500-2000 neurons) with interpretable higher-order interac...
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Realizing Common Random Numbers: Event-Keyed Hashing for Causally Valid Stochastic Models
This paper addresses the critical problem that standard stateful PRNG implementations in agent-based models violate causal validity by making random d...
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A Standardized Framework for Evaluating Gene Expression Generative Models
This paper addresses the critical lack of standardized evaluation protocols for single-cell gene expression generative models, where inconsistent metr...
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Single Molecule Localization Microscopy Challenge: A Biologically Inspired Benchmark for Long-Sequence Modeling
This paper addresses the core challenge of evaluating state-space models on biologically realistic, sparse, and stochastic temporal processes, which a...
Realizing Common Random Numbers: Event-Keyed Hashing for Causally Valid Stochastic Models
Institute for Disease Modeling, Gates Foundation | Department of Epidemiology, University of North Carolina | Institute for Disease Modeling, Gates Foundation
30秒速读
IN SHORT: This paper addresses the critical problem that standard stateful PRNG implementations in agent-based models violate causal validity by making random draws execution-path-dependent, thereby breaking the fundamental assumption of common random numbers needed for valid counterfactual comparisons.
核心创新
- Methodology Identifies and formalizes the fundamental mismatch between scientific causal structure in ABMs and program-level causal structure induced by stateful PRNGs through the lens of Structural Causal Models (SCMs)
- Methodology Introduces the concept of 'execution invariance' as a necessary property for causally valid ABM counterfactuals, requiring that exogenous noise terms remain stable across intervention scenarios
- Methodology Proposes event-keyed random number generation combining counter-based PRNGs (Philox/Threefry) with event identifiers to decouple random draws from simulation execution order
主要结论
- Standard stateful PRNG practices violate the execution invariance required for valid SCM-style interventions, as demonstrated through formal analysis of the structural causal model framework
- Event-keyed hashing with counter-based PRNGs restores the stable event-indexed exogenous structure assumed by SCMs, enabling proper counterfactual comparisons with variance reduction benefits
- The proposed approach allows ABMs to function as valid structural causal models under interventions, maintaining the critical property that interventions change only structural equations while holding exogenous noise terms fixed
摘要: Agent-based models (ABMs) are widely used to estimate causal treatment effects via paired counterfactual simulation. A standard variance reduction technique is common random numbers (CRNs), which couples replicates across intervention scenarios by sharing the same random inputs. In practice, CRNs are implemented by reusing the same base seed, but this relies on a critical assumption: that the same draw index corresponds to the same modeled event across scenarios. Stateful pseudorandom number generators (PRNGs) violate this assumption whenever interventions alter the simulation's execution path, because any change in control flow shifts the draw index used for all downstream events. We argue that this execution-path-dependent draw indexing is not only a variance-reduction nuisance, but represents a fundamental mismatch between the scientific causal structure ABMs are intended to encode and the program-level causal structure induced by stateful PRNG implementations. Formalizing this through the lens of structural causal models (SCMs), we show that standard PRNG practices yield causally incoherent paired counterfactual comparisons even when the mechanistic specification is otherwise sound. We show that a remedy is to combine counter-based random number generators (e.g., Philox/Threefry) with event identifiers. This decouples random number generation from simulation execution order by making random draws explicit functions of the particular modeled event that called them, restoring the stable event-indexed exogenous structure assumed by SCMs.