arXiv subjects

Mingyuan Yan

Publications and source records attributed to Mingyuan Yan.

6 recordsLinked to original sources

arXiv2026

Learning-Driven Adaptive Audit Scheduling: A Sequential Decision Approach to Off-Chain Data Integrity

We model cryptographic auditing of off-chain data as a Constrained MDP (CMDP) under partial observability: the storage node's hidden type and corruption state make the problem a POMDP, while a miss-rate ceiling rho imposes an explicit security constraint. We propose DRQN-CMDP, a Deep Recurrent Q-Network whose GRU layer maintains a belief over the latent node type, paired with Lagrangian dual ascent that adapts the miss-rate penalty lambda automatically. A pairing-free homomorphic-MAC primitive supplies O(1) on-chain verification cost. Across 13 methods--four DQN variants, PPO, A2C, PPO-Lagrangian, a stateful Bayesian heuristic, three fixed-rule baselines, and an oracle-informed heuristic--DRQN-CMDP achieves a favourable balance: 83% lower gas than fixed high-frequency auditing, single-digit miss rate (7.5%), and moderate detection latency--a combination no other method matches across all three objectives simultaneously.

cs.AI↗

arXiv2026

Switching-Reference Voltage Control for Distribution Systems with AI-Training Data Centers

Large-scale AI training workloads in data centers exhibit rapid and periodic power swings that can induce voltage deviations in power distribution systems. Existing voltage controllers treat these swings as a generic disturbance, leading to high control effort but still large voltage violations. However, such emerging loads are not random: they alternate between two distinct operating phases. This paper exploits this structure with a decentralized switching-reference voltage control framework. By switching each voltage reference in step with the workload phases, the controller cancels the phase-induced voltage shift, holding the voltage within limits with low control effort. Because real-time communication between buses is not always available, the controller is designed to infer the reference from local voltage measurements. This paper further proves convergence under deadband and saturation. In case studies on real AI training power traces, the switching reference suppresses voltage violations, sometimes eliminating them entirely, while reducing the control effort by approximately an order of magnitude compared with conventional droop control. Further experiments confirm that it remains effective with multiple data centers and internal load smoothing.

eess.SY↗

arXiv2024

Heterogeneous Entity Representation for Medicinal Synergy Prediction

Medicinal synergy prediction is a powerful tool in drug discovery and development that harnesses the principles of combination therapy to enhance therapeutic outcomes by improving efficacy, reducing toxicity, and preventing drug resistance. While a myriad of computational methods has emerged for predicting synergistic drug combinations, a large portion of them may overlook the intricate, yet critical relationships between various entities in drug interaction networks, such as drugs, cell lines, and diseases. These relationships are complex and multidimensional, requiring sophisticated modeling to capture nuanced interplay that can significantly influence therapeutic efficacy. We introduce a salient deep hypergraph learning method, namely, Heterogeneous Entity Representation for MEdicinal Synergy prediction (HERMES), to predict anti-cancer drug synergy. HERMES integrates heterogeneous data sources, encompassing drug, cell line, and disease information, to provide a comprehensive understanding of the interactions involved. By leveraging advanced hypergraph neural networks with gated residual mechanisms, HERMES can effectively learn complex relationships/interactions within the data. Our results show HERMES demonstrates state-of-the-art performance, particularly in forecasting new drug combinations, significantly surpassing previous methods. This advancement underscores the potential of HERMES to facilitate more effective and precise drug combination predictions, thereby enhancing the development of novel therapeutic strategies.

cs.CE↗

arXiv2024

Improving Discrete Optimisation Via Decoupled Straight-Through Estimator

The Straight-Through Estimator (STE) is the dominant method for training neural networks with discrete variables, enabling gradient-based optimisation by routing gradients through a differentiable surrogate. However, existing STE variants conflate two fundamentally distinct concerns: forward-pass stochasticity, which controls exploration and latent space utilisation, and backward-pass gradient dispersion i.e how learning signals are distributed across categories. We show that these concerns are qualitatively different and that tying them to a single temperature parameter leaves significant performance gains untapped. We propose Decoupled Straight-Through (Decoupled ST), a minimal modification that introduces separate temperatures for the forward pass ($\tau_f$) and the backward pass ($\tau_b$). This simple change enables independent tuning of exploration and gradient dispersion. Across three diverse tasks (Stochastic Binary Networks, Categorical Autoencoders, and Differentiable Logic Gate Networks), Decoupled ST consistently outperforms Identity STE, Softmax STE, and Straight-Through Gumbel-Softmax. Crucially, optimal $(\tau_f, \tau_b)$ configurations lie far off the diagonal $\tau_f = \tau_b$, confirming that the two concerns do require different answers and that single-temperature methods are fundamentally constrained.

cs.LG↗

arXiv2024

Gaussian Mixture Vector Quantization with Aggregated Categorical Posterior

The vector quantization is a widely used method to map continuous representation to discrete space and has important application in tokenization for generative mode, bottlenecking information and many other tasks in machine learning. Vector Quantized Variational Autoencoder (VQ-VAE) is a type of variational autoencoder using discrete embedding as latent. We generalize the technique further, enriching the probabilistic framework with a Gaussian mixture as the underlying generative model. This framework leverages a codebook of latent means and adaptive variances to capture complex data distributions. This principled framework avoids various heuristics and strong assumptions that are needed with the VQ-VAE to address training instability and to improve codebook utilization. This approach integrates the benefits of both discrete and continuous representations within a variational Bayesian framework. Furthermore, by introducing the \textit{Aggregated Categorical Posterior Evidence Lower Bound} (ALBO), we offer a principled alternative optimization objective that aligns variational distributions with the generative model. Our experiments demonstrate that GM-VQ improves codebook utilization and reduces information loss without relying on handcrafted heuristics.

cs.LG↗

arXiv2024

VQSynery: Robust Drug Synergy Prediction With Vector Quantization Mechanism

The pursuit of optimizing cancer therapies is significantly advanced by the accurate prediction of drug synergy. Traditional methods, such as clinical trials, are reliable yet encumbered by extensive time and financial demands. The emergence of high-throughput screening and computational innovations has heralded a shift towards more efficient methodologies for exploring drug interactions. In this study, we present VQSynergy, a novel framework that employs the Vector Quantization (VQ) mechanism, integrated with gated residuals and a tailored attention mechanism, to enhance the precision and generalizability of drug synergy predictions. Our findings demonstrate that VQSynergy surpasses existing models in terms of robustness, particularly under Gaussian noise conditions, highlighting its superior performance and utility in the complex and often noisy domain of drug synergy research. This study underscores the potential of VQSynergy in revolutionizing the field through its advanced predictive capabilities, thereby contributing to the optimization of cancer treatment strategies.

q-bio.QM↗