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Kyle C. Nguyen

Publications and source records attributed to Kyle C. Nguyen.

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Observable-Reduction-Guided Sparse Regression for Partially Observed Active-Quiescent Systems

Active-quiescent switching occurs in biological populations in which growth is confined to a proliferative active state, while cells may reversibly enter a nonproliferative quiescent state. Experiments often observe only part of this process, through active-state markers, aggregate population measurements, or aggregate data supplemented by sparse active-state observations. Such measurements arise when marker panels are limited, active-state assays require fixation or endpoint sampling, or only total cell number, optical density, tumor burden, or aggregate fluorescence is reported. These observation choices complicate sparse regression methods such as sparse identification of nonlinear dynamics (SINDy), because the measured variable may satisfy a different equation from the underlying active-quiescent system. A library chosen for the wrong observable may therefore fit a trajectory without preserving mechanistic interpretation or transferability. We study this issue using a two-compartment ordinary differential equation model. We define observable reduction as the elimination of hidden states to obtain the differential equation satisfied by the measured variable. For several biologically relevant growth laws, we derive observation-specific reductions and use them to construct sparse-regression libraries. Using synthetic data, we compare these structured libraries with standard polynomial SINDy. Polynomial libraries can match training trajectories while failing coefficient-relation and transfer tests, whereas reduction-guided libraries recover interpretable coefficient maps when the observed regime is informative. These results show that interpretable equation learning in hidden-compartment systems requires matching both the regression target and candidate library to the observation process.

math.DS

ABM-UDE: Developing Surrogates for Epidemic Agent-Based Models via Scientific Machine Learning

Agent-based epidemic models (ABMs) encode behavioral and policy heterogeneity but are too slow for nightly hospital planning. We develop county-ready surrogates that learn directly from exascale ABM trajectories using Universal Differential Equations (UDEs): mechanistic SEIR-family ODEs with a neural-parameterized contact rate $\kappa_\phi(u,t)$ (no additive residual). Our contributions are threefold: we adapt multiple shooting and an observer-based prediction-error method (PEM) to stabilize identification of neural-augmented epidemiological dynamics across intervention-driven regime shifts; we enforce positivity and mass conservation and show the learned contact-rate parameterization yields a well-posed vector field; and we quantify accuracy, calibration, and compute against ABM ensembles and UDE baselines. On a representative ExaEpi scenario, PEM-UDE reduces mean MSE by 77% relative to single-shooting UDE (3.00 vs. 13.14) and by 20% relative to MS-UDE (3.75). Reliability improves in parallel: empirical coverage of ABM $10$-$90$% and $25$-$75$% bands rises from 0.68/0.43 (UDE) and 0.79/0.55 (MS-UDE) to 0.86/0.61 with PEM-UDE and 0.94/0.69 with MS+PEM-UDE, indicating calibrated uncertainty rather than overconfident fits. Inference runs in seconds on commodity CPUs (20-35 s per $\sim$90-day forecast), enabling nightly ''what-if'' sweeps on a laptop. Relative to a $\sim$100 CPU-hour ABM reference run, this yields $\sim10^{4}\times$ lower wall-clock per scenario. This closes the realism-cadence gap, supports threshold-aware decision-making (e.g., maintaining ICU occupancy $<75$%), preserves mechanistic interpretability, and enables calibrated, risk-aware scenario planning on standard institutional hardware. Beyond epidemics, the ABM$\to$UDE recipe provides a portable path to distill agent-based simulators into fast, trustworthy surrogates for other scientific domains.

cs.LG