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George Vega Yon

Publications and source records attributed to George Vega Yon.

2 recordsLinked to original sources

Generalized Machine Learning for Fast Calibration of Agent-Based Epidemic Models

Agent-based models (ABMs) are widely used to study infectious disease dynamics, but their calibration is often computationally intensive, limiting their applicability in time-sensitive public health settings. We propose DeepIMC (Deep Inverse Mapping Calibration), a machine learning-based calibration framework that directly learns the inverse mapping from epidemic time series to epidemiological parameters. DeepIMC trains a bidirectional Long Short-Term Memory (BiLSTM) neural network on synthetic epidemic trajectories generated from agent-based models such as the Susceptible-Infected-Recovered (SIR) model, enabling rapid parameter estimation without repeated simulation at inference time. We evaluate DeepIMC through an extensive simulation study comprising 5,000 heterogeneous epidemic scenarios and benchmark its performance against Approximate Bayesian Computation (ABC) using likelihood-free Markov Chain Monte Carlo. The results show that DeepIMC substantially improves parameter recovery accuracy, produces sharp and well-calibrated predictive intervals, and reduces computational time by more than an order of magnitude relative to ABC. Although structural parameter identifiability constraints limit the precise recovery of all model parameters simultaneously, the calibrated models reliably reproduce epidemic trajectories and support accurate forward prediction with their estimated parameters. DeepIMC is implemented in the open-source R package epiworldRCalibrate, facilitating practical adoption for real-time epidemic modeling and policy analysis. Overall, our findings demonstrate that DeepIMC provides a scalable, operationally effective alternative to traditional simulation-based calibration methods for agent-based epidemic models.

cs.LG↗

A novel approach for classifying Monoamine Neurotransmitters by applying Machine Learning on UV plasmonic-engineered Auto Fluorescence Time Decay Series (AFTDS)

This study introduces a hybrid approach integrating advanced plasmonic nanomaterials and machine learning (ML) for high-precision biomolecule detection. We leverage aluminum concave nanocubes (AlCNCs) as an innovative plasmonic substrate to enhance the native fluorescence of neurotransmitters, including dopamine (DA), norepinephrine (NE), and 3,4-Dihydroxyphenylacetic acid (DOPAC). AlCNCs amplify weak fluorescence signals, enabling probe-free, label-free detection and differentiation of these molecules with great sensitivity and specificity. To further improve classification accuracy, we employ ML algorithms, with Long Short-Term Memory (LSTM) networks playing a central role in analyzing time-dependent fluorescence data. Comparative evaluations with k-Nearest Neighbors (KNN) and Random Forest (RF) demonstrate the superior performance of LSTM in distinguishing neurotransmitters. The results reveal that AlCNC substrates provide up to a 12-fold enhancement in fluorescence intensity for DA, 9-fold for NE, and 7-fold for DOPAC compared to silicon substrates. At the same time, ML algorithms achieve classification accuracy exceeding 89%. This interdisciplinary methodology bridges the gap between nanotechnology and ML, showcasing the synergistic potential of AlCNC-enhanced native fluorescence and ML in biosensing. The framework paves the way for probe-free, label-free biomolecule profiling, offering transformative implications for biomedical diagnostics and neuroscience research.

q-bio.BM↗