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Debnath Pal

Publications and source records attributed to Debnath Pal.

3 recordsLinked to original sources

Robust Lightweight Deep Learning Models for Oral Cancer Screening

Oral cancer is a leading cause of mortality in low-to-middle-income countries, where a shortage of specialists delays diagnosis. While point-of-care screening via smartphones offers a scalable solution, developing robust AI for resource-constrained settings poses significant challenges, including class imbalance in training data, variable data quality, and computational constraints on edge devices. In this paper, we present the optimisation of lightweight deep learning models for smartphone-based oral cancer screening. Using a diverse, multi-centre retrospective dataset of approximately 30,000 images acquired over a decade, we systematically evaluate state-of-the-art convolutional, transformer, and hybrid architectures. Through rigorous pipeline ablation, we demonstrate that directly optimising hybrid architectures for the edge strictly outperforms computationally heavy paradigms, such as large models or knowledge distillation. Furthermore, interpretability analysis and simulated noise-stress tests revealed that the system anchors on clinical features and remains robust to unstructured sensor noise, despite vulnerabilities to impulse bit errors. In the held-out test set, our optimised MobileViTv2 models achieved an average sensitivity of 83.2 $\pm$ 1.5% and an average specificity of 86.0 $\pm$ 0.8%, with the best model exhibiting 87.4% sensitivity, 86.5% specificity, and a critical negative predictive value of 97.2% with reference to specialist labels. These results confirm that with targeted architectural selection and streamlined optimisation, interpretable and robust lightweight AI models exhibit high potential for edge deployment to enable automated triage in primary care settings.

cs.AI

Action-Inspired Generative Models

We introduce Action-Inspired Generative Models (AGMs), a dual-network generative framework motivated by the observation that existing bridge-matching methods assign uniform regression weight to every stochastic transition in the transport landscape, regardless of whether a given bridge sample lies along a structurally coherent trajectory or a degenerate one. We address this by introducing a lightweight learned scalar potential $V_\phi$ that scores bridge samples online and modulates the drift objective via importance weights derived through a stop-gradient barrier -- preventing adversarial feedback between the two networks whilst preserving $V_\phi$'s guiding signal. Crucially, $V_\phi$ comprises only $\sim$1.4% of the primary drift network's parameter count, adds no overhead to the inference graph, and requires no iterative half-bridge fitting or auxiliary stochastic differential equation (SDE) solvers: it is a plug-and-play enhancement to any bridge-matching training loop. At inference, $V_\phi$ is discarded entirely, leaving standard Euler-Maruyama integration of the exponential moving average (EMA) drift. We demonstrate that selectively penalising uninformative transport paths through the learned potential yields consistent improvements in generation quality across fidelity and coverage metrics.

cs.LG

Metapopulation dynamics of a respiratory disease with infection during travel

We formulate a compartmental model for the propagation of a respiratory disease in a patchy environment. The patches are connected through the mobility of individuals, and we assume that disease transmission and recovery are possible during travel. Moreover, the migration terms are assumed to depend on the distance between patches and the perceived severity of the disease. The positivity and boundedness of the model solutions are discussed. We analytically show the existence and global asymptotic stability of the disease-free equilibrium. We study three different network topologies numerically and find that underlying network structure is crucial for disease transmission. Further numerical simulations reveal that infection during travel has the potential to change the stability of disease-free equilibrium from stable to unstable. The coupling strength and transmission coefficients are also very crucial in disease propagation. Different exit screening scenarios indicate that the patch with the highest prevalence may have adverse effects but other patches will be benefited from exit screening. Furthermore, while studying the multi-strain dynamics, it is observed that two co-circulating strains will not persist simultaneously in the community but only one of the strains may persist in the long run. Transmission coefficients corresponding to the second strain are very crucial and show threshold like behavior with respect to the equilibrium density of the second strain.

q-bio.PE