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Zekai Chen

Publications and source records attributed to Zekai Chen.

At least 37 records · Page 2Linked to original sources
arXiv2026

Towards Modality-imbalanced Federated Graph Learning: A Data Synthesis-based Approach

MultiModal Federated Graph Learning (MM-FGL) offers a natural collaborative training paradigm, but its practical deployment is challenged by two granularities of modality imbalance. Client-level imbalance occurs when certain clients lack entire modalities, while node-level imbalance occurs when individual nodes exhibit missing visual or textual attributes. While several relevant studies exist, our investigation reveals that they predominantly target graph-agnostic or centralized scenarios, rendering them difficult to adapt directly. To address these challenges, we formalize modality-imbalanced MM-FGL as an implicit graph-aware latent semantic representation synthesis problem. This paradigm recovers missing modal semantics directly within the representation space, thereby maximizing alignment with the original data's semantic distribution and mitigating the high variance induced by missing modalities. To this end, we propose FedMGS (Federated Modality-aware Graph Synthesis), which integrates three core components. The availability-aware graph encoder prevents missing modalities from contaminating local structural propagation. The prototype-guided latent semantic synthesizer establishes cross-client semantic anchors for unavailable modalities. The reliability-calibrated semantic fusion mechanism regulates the impact of recovered latent representations prior to predictive readout. Extensive experiments on four tasks show that FedMGS consistently outperforms competitive baselines with gains up to 17.41% with best efficiency-performance tradeoff.

cs.LG↗
arXiv2026

PRISM: Topology-Aware Cross-Modal Imputation for Modality-Deficient Federated Graph Learning

Multimodal federated graph learning (MM-FGL) aims to collaboratively learn from decentralized graphs with text and images. However, real-world clients may not share a common modality basis: a visual-search client may contain image--interaction graphs but no seller descriptions, while a catalog client may provide text but no product images. We refer to this practical setting as client-level modality deficiency. Unlike random instance-wise missingness, a deficient client lacks the local semantic basis needed to reconstruct the absent modality. More importantly, in graph learning, incomplete representations initialize message passing, so imputation errors can be filtered, mixed, and amplified by the receiving topology. To address this gap, we propose \textbf{PRISM} (\textbf{P}roactive \textbf{R}etrieval and \textbf{I}mputation via \textbf{S}tructural \textbf{M}eta-prompting), a topology-aware federated cross-modal imputation framework. Rather than reconstructing the missing modality solely from local observations, PRISM recovers missing-modality semantics from the federation and introduces them into local graph propagation under topology-aware control. Experiments on six multimodal graph datasets across graph-centric and modality-centric tasks show that PRISM consistently improves modality-deficient clients, outperforming state-of-the-art baselines by \textbf{4.48}\% on average.

cs.LG↗
arXiv2026

Interaction-enabled metal-insulator phase transition in a driven quantum gas

Particle transport and energy flow are central to a wide range of phenomena in the natural sciences. While interactions generically promote ergodicity and diffusion, quantum interference can arrest transport, defying classical expectations. Here, we experimentally investigate their interplay in a periodically driven 3D quantum gas with tunable interactions. Strikingly, we find a sharp dynamical boundary separating localization from diffusive energy absorption. By tuning the driving amplitude and interaction strength, we map the localization-delocalization phase diagram and characterize this boundary via finite-time scaling. On the insulating side, we observe many-body dynamical localization (MBDL) featuring arrested momentum-space transport. Transport becomes subdiffusive near the boundary and diffusive in the delocalized regime, yielding a metal-insulator transition that we interpret as localization in many-body Hilbert space. Our results exemplify an interaction-enabled dynamical phase transition in a closed Floquet many-body system, and clarify how coherence and interactions jointly govern the quantum-to-classical transition.

cond-mat.quant-gas↗
arXiv2026

CG-MambaNet: A spatiotemporal framework for cross-patient epileptic seizure prediction using CNN-GCN-Mamba-BiLSTM with event-level clinical evaluation

Epileptic seizure prediction from scalp EEG is critical for closed-loop neurostimulation therapy. Existing deep-learning methods share two architectural limitations: they model EEG channels independently, neglecting inter-channel spatial synchrony, and process raw time-domain samples without frequency decomposition. A methodological limitation also affects the field: most studies use data splits that permit patient-level information leakage, yielding optimistic estimates that do not generalise to unseen patients. We present CG-MambaNet, a spatiotemporal seizure prediction framework addressing all three limitations. A depthwise separable CNN front-end decomposes each EEG patch into multi-scale spectro-temporal features, capturing delta-to-gamma band dynamics before sequence modelling. A two-layer graph convolutional network with a learnable adjacency matrix captures inter-channel functional synchrony without montage-specific coordinates, applicable to bipolar (CHB-MIT) and referential (SIENA) montages. A bidirectional Mamba encoder followed by a bidirectional LSTM models long- and short-range temporal dynamics, and a two-layer MLP produces the final seizure probability. This serial hierarchy ensures frequency decomposition precedes spatial mixing, which precedes temporal integration. Under strict leave-one-patient-out cross-validation with five independent random seeds, CG-MambaNet achieves AUC-ROC of 0.8152+/-0.0176 on CHB-MIT (n=22) and 0.7104+/-0.0261 on SIENA (n=6), surpassing all published cross-patient methods without domain adaptation. An event-level evaluation framework merging consecutive alarmed windows via a persistence filter reduces false predictions to 0.32 alarms/hour on CHB-MIT, demonstrating clinically meaningful alarm burden.

eess.SP↗
arXiv2026

Constacyclic codes with best-known parameters

In this paper, we construct several infinite families of $q$-ary constacyclic codes over a finite field $\mathbb{F}_q$ with length $n$, dimension around $n/2$, and minimum distance at least $cn/\log_q n$ for some positive constant $c$. They contain many constacyclic codes with optimal, or almost-optimal, or best-known parameters. We also consider constacyclic codes of various lengths.

cs.IT↗
arXiv2026

STAGE: Tackling Semantic Drift in Multimodal Federated Graph Learning

Federated graph learning (FGL) enables collaborative training on graph data across multiple clients. As graph data increasingly contain multimodal node attributes such as text and images, multimodal federated graph learning (MM-FGL) has become an important yet substantially harder setting. The key challenge is that clients from different modality domains may not share a common semantic space: even for the same concept, their local encoders can produce inconsistent representations before collaboration begins. This makes direct parameter coordination unreliable and further causes two downstream problems: forcing heterogeneous client representations into a naively shared semantic space may create false semantic agreement, and graph message passing may amplify residual inconsistency across neighborhoods. To address this issue, we propose \textbf{STAGE}, a protocol-first framework for MM-FGL. Instead of relying on direct parameter averaging, STAGE builds a shared semantic space that first translates heterogeneous multimodal features into comparable representations and then regulates how these representations propagate over local graph structures. In this way, STAGE not only improves cross-client semantic calibration, but also reduces the risk of inconsistency amplification during graph learning. Extensive experiments on 8 multimodal-attributed graphs across 5 graph-centric and modality-centric tasks show that STAGE consistently achieves state-of-the-art performance while reducing per-round communication payload.

cs.LG↗
arXiv2026

Towards Robust Federated Multimodal Graph Learning under Modality Heterogeneity

Recently, multimodal graph learning (MGL) has garnered significant attention for integrating diverse modality information and structured context to support various network applications. However, real-world graphs are often isolated due to data-sharing limitations across multiple parties, and their modalities are frequently incomplete. This highlights an urgent need to develop a robust federated approach. However, we find that existing methods remain insufficient. On the one hand, centralized MGL methods that handle missing modalities overlook the knowledge sharing and generalization in federated scenarios. On the other hand, while federated MGL methods have become increasingly mature, they primarily target non-graph data. Based on these technologies, we identify a two-stage pipeline wherein client-side completion reconstructs missing modalities, and server-side aggregation integrates the client-updated parameters of both the modality generator and the backbone models. Although this serves as a general solution, we identify two primary challenges in achieving greater robustness: (1) Topology-Isolated Local Completion: Client-side modality generation struggles to effectively leverage global semantics. (2) Reliability-Imbalanced Global Aggregation: Server-side multi-party collaboration is hindered by client updates with varying modality availability and recovery reliability. To address these challenges, we propose \textsc{FedMPO}, which utilizes topology-aware cross-modal generation to recover missing features using comprehensive graph context, missing-aware expert routing to locally filter out noisy recovered signals, and reliability-aware aggregation to appropriately down-weight unreliable updates. Extensive experiments on 3 tasks across 6 datasets demonstrate that FedMPO outperforms baselines, achieving performance gains of up to 4.10% and 5.65% in high-missing and non-IID settings.

cs.LG↗
arXiv2026

Origin and emergent features of many-body dynamical localization

The question of whether interactions can break dynamical localization in quantum kicked rotor systems has been the subject of a long--standing debate. Here, we introduce an extended mapping from the kicked Lieb--Liniger model to a high--dimensional lattice model and reveal universal features: on--site pseudorandomness and hybrid exponential--algebraic decay couplings with increasing momenta. We find that the exponent and the amplitude of the algebraic decay undergo a crossover as the interaction strength increases. This mapping uncovers the origin of dynamical localization and the interaction effect on the integrability of the system. An analysis of the generalized fractal dimension and level--spacing ratio supports these findings, highlighting the presence of near integrability and multifractality in different regions of parameter space. Our results offer an explanation for the occurrence of many--body dynamical localization, particularly in strongly correlated quantum gases, and are anticipated to generalize to systems of many particles.

cond-mat.quant-gas↗
arXiv2026

OpenDDI: A Comprehensive Benchmark for DDI Prediction

Drug-Drug Interactions (DDIs) significantly influence therapeutic efficacy and patient safety. As experimental discovery is resource-intensive and time-consuming, efficient computational methodologies have become essential. The predominant paradigm formulates DDI prediction as a drug graph-based link prediction task. However, further progress is hindered by two fundamental challenges: (1) lack of high-quality data: most studies rely on small-scale DDI datasets and single-modal drug representations; (2) lack of standardized evaluation: inconsistent scenarios, varied metrics, and diverse baselines. To address the above issues, we propose OpenDDI, a comprehensive benchmark for DDI prediction. Specifically, (1) from the data perspective, OpenDDI unifies 6 widely used DDI datasets and 2 existing forms of drug representation, while additionally contributing 3 new large-scale LLM-augmented datasets and a new multimodal drug representation covering 5 modalities. (2) From the evaluation perspective, OpenDDI unifies 20 SOTA model baselines across 3 downstream tasks, with standardized protocols for data quality, effectiveness, generalization, robustness, and efficiency. Based on OpenDDI, we conduct a comprehensive evaluation and derive 10 valuable insights for DDI prediction while exposing current limitations to provide critical guidance for this rapidly evolving field. Our code is available at https://github.com/xiaoriwuguang/OpenDDI

cs.LG↗
arXiv2026

LION: A Clifford Neural Paradigm for Multimodal-Attributed Graph Learning

Recently, the rapid advancement of multimodal domains has driven a data-centric paradigm shift in graph ML, transitioning from text-attributed to multimodal-attributed graphs. This advancement significantly enhances data representation and expands the scope of graph downstream tasks, such as modality-oriented tasks, thereby improving the practical utility of graph ML. Despite its promise, limitations exist in the current neural paradigms: (1) Neglect Context in Modality Alignment: Most existing methods adopt topology-constrained or modality-specific operators as tokenizers. These aligners inevitably neglect graph context and inhibit modality interaction, resulting in suboptimal alignment. (2) Lack of Adaptation in Modality Fusion: Most existing methods are simple adaptations for 2-modality graphs and fail to adequately exploit aligned tokens equipped with topology priors during fusion, leading to poor generalizability and performance degradation. To address the above issues, we propose LION (c\underline{LI}ff\underline{O}rd \underline{N}eural paradigm) based on the Clifford algebra and decoupled graph neural paradigm (i.e., propagation-then-aggregation) to implement alignment-then-fusion in multimodal-attributed graphs. Specifically, we first construct a modality-aware geometric manifold grounded in Clifford algebra. This geometric-induced high-order graph propagation efficiently achieves modality interaction, facilitating modality alignment. Then, based on the geometric grade properties of aligned tokens, we propose adaptive holographic aggregation. This module integrates the energy and scale of geometric grades with learnable parameters to improve modality fusion. Extensive experiments on 9 datasets demonstrate that LION significantly outperforms SOTA baselines across 3 graph and 3 modality downstream tasks.

cs.AI↗
arXiv2026

The Patient is not a Moving Document: A World Model Training Paradigm for Longitudinal EHR

Large language models (LLMs) trained with next-word-prediction have achieved success as clinical foundation models. Representations from these language backbones yield strong linear probe performance across biomedical tasks, suggesting that patient semantics emerge from next-token prediction at scale. However, this paradigm treats patients as a document to be summarized rather than a dynamical system to be simulated; a patient's trajectory emerges from their state evolving under interventions and time, requiring models that simulate dynamics rather than predict tokens. To address this, we introduce SMB-Structure, a world model for structured EHR that grounds a joint-embedding prediction architecture (JEPA) with next-token prediction (SFT). SFT grounds our model to reconstruct future patient states in token space, while JEPA predicts those futures in latent space from the initial patient representation alone, forcing trajectory dynamics to be encoded before the next state is observed. We validate across two large-scale cohorts: Memorial Sloan Kettering (23,319 oncology patients; 323,000+ patient-years) and INSPECT (19,402 pulmonary embolism patients). Using a linear probe evaluated at multiple points along the disease trajectory, we demonstrate that our training paradigm learns embeddings that capture disease dynamics not recoverable by autoregressive baselines, enabling SMB-Structure to achieve competitive performance on complex tasks characterized by high patient heterogeneity. Model weights are available at https://huggingface.co/standardmodelbio/SMB-v1-1.7B-Structure.

cs.AI↗
arXiv2026

BoostFGL: Boosting Fairness in Federated Graph Learning

Federated graph learning (FGL) enables collaborative training of graph neural networks (GNNs) across decentralized subgraphs without exposing raw data. While existing FGL methods often achieve high overall accuracy, we show that this average performance can conceal severe degradation on disadvantaged node groups. From a fairness perspective, these disparities arise systematically from three coupled sources: label skew toward majority patterns, topology confounding in message propagation, and aggregation dilution of updates from hard clients. To address this, we propose \textbf{BoostFGL}, a boosting-style framework for fairness-aware FGL. BoostFGL introduces three coordinated mechanisms: \ding{182} \emph{Client-side node boosting}, which reshapes local training signals to emphasize systematically under-served nodes; \ding{183} \emph{Client-side topology boosting}, which reallocates propagation emphasis toward reliable yet underused structures and attenuates misleading neighborhoods; and \ding{184} \emph{Server-side model boosting}, which performs difficulty- and reliability-aware aggregation to preserve informative updates from hard clients while stabilizing the global model. Extensive experiments on 9 datasets show that BoostFGL delivers substantial fairness gains, improving Overall-F1 by 8.43\%, while preserving competitive overall performance against strong FGL baselines.

cs.LG↗
arXiv2026

DANCE: Dynamic, Available, Neighbor-gated Condensation for Federated Text-Attributed Graphs

Federated graph learning (FGL) enables collaborative training on graph data across multiple clients. With the rise of large language models (LLMs), textual attributes in FGL graphs are gaining attention. Text-attributed graph federated learning (TAG-FGL) improves FGL by explicitly leveraging LLMs to process and integrate these textual features. However, current TAG-FGL methods face three main challenges: \textbf{(1) Overhead.} LLMs for processing long texts incur high token and computation costs. To make TAG-FGL practical, we introduce graph condensation (GC) to reduce computation load, but this choice also brings new issues. \textbf{(2) Suboptimal.} To reduce LLM overhead, we introduce GC into TAG-FGL by compressing multi-hop texts/neighborhoods into a condensed core with fixed LLM surrogates. However, this one-shot condensation is often not client-adaptive, leading to suboptimal performance. \textbf{(3) Interpretability.} LLM-based condensation further introduces a black-box bottleneck: summaries lack faithful attribution and clear grounding to specific source spans, making local inspection and auditing difficult. To address the above issues, we propose \textbf{DANCE}, a new TAG-FGL paradigm with GC. To improve \textbf{suboptimal} performance, DANCE performs round-wise, model-in-the-loop condensation refresh using the latest global model. To enhance \textbf{interpretability}, DANCE preserves provenance by storing locally inspectable evidence packs that trace predictions to selected neighbors and source text spans. Across 8 TAG datasets, DANCE improves accuracy by \textbf{2.33\%} at an \textbf{8\%} condensation ratio, with \textbf{33.42\%} fewer tokens than baselines.

cs.LG↗
arXiv2025

PrivGNN: High-Performance Secure Inference for Cryptographic Graph Neural Networks

Graph neural networks (GNNs) are powerful tools for analyzing and learning from graph-structured (GS) data, facilitating a wide range of services. Deploying such services in privacy-critical cloud environments necessitates the development of secure inference (SI) protocols that safeguard sensitive GS data. However, existing SI solutions largely focus on convolutional models for image and text data, leaving the challenge of securing GNNs and GS data relatively underexplored. In this work, we design, implement, and evaluate $\sysname$, a lightweight cryptographic scheme for graph-centric inference in the cloud. By hybridizing additive and function secret sharings within secure two-party computation (2PC), $\sysname$ is carefully designed based on a series of novel 2PC interactive protocols that achieve $1.5\times \sim 1.7\times$ speedups for linear layers and $2\times \sim 15\times$ for non-linear layers over state-of-the-art (SotA) solutions. A thorough theoretical analysis is provided to prove $\sysname$'s correctness, security, and lightweight nature. Extensive experiments across four datasets demonstrate $\sysname$'s superior efficiency with $1.3\times \sim 4.7\times$ faster secure predictions while maintaining accuracy comparable to plaintext graph property inference.

cs.CR↗
arXiv2025

MagicDock: Toward Docking-oriented De Novo Ligand Design via Gradient Inversion

De novo ligand design is a fundamental task that seeks to generate protein or molecule candidates that can effectively dock with protein receptors and achieve strong binding affinity entirely from scratch. It holds paramount significance for a wide spectrum of biomedical applications. However, most existing studies are constrained by the \textbf{Pseudo De Novo}, \textbf{Limited Docking Modeling}, and \textbf{Inflexible Ligand Type}. To address these issues, we propose MagicDock, a forward-looking framework grounded in the progressive pipeline and differentiable surface modeling. (1) We adopt a well-designed gradient inversion framework. To begin with, general docking knowledge of receptors and ligands is incorporated into the backbone model. Subsequently, the docking knowledge is instantiated as reverse gradient flows by binding prediction, which iteratively guide the de novo generation of ligands. (2) We emphasize differentiable surface modeling in the docking process, leveraging learnable 3D point-cloud representations to precisely capture binding details, thereby ensuring that the generated ligands preserve docking validity through direct and interpretable spatial fingerprints. (3) We introduce customized designs for different ligand types and integrate them into a unified gradient inversion framework with flexible triggers, thereby ensuring broad applicability. Moreover, we provide rigorous theoretical guarantees for each component of MagicDock. Extensive experiments across 9 scenarios demonstrate that MagicDock achieves average improvements of 27.1\% and 11.7\% over SOTA baselines specialized for protein or molecule ligand design, respectively.

cs.LG↗
arXiv2025

GenVarFormer: Predicting gene expression from long-range mutations in cancer

Distinguishing the rare "driver" mutations that fuel cancer progression from the vast background of "passenger" mutations in the non-coding genome is a fundamental challenge in cancer biology. A primary mechanism that non-coding driver mutations contribute to cancer is by affecting gene expression, potentially from millions of nucleotides away. However, existing predictors of gene expression from mutations are unable to simultaneously handle interactions spanning millions of base pairs, the extreme sparsity of somatic mutations, and generalize to unseen genes. To overcome these limitations, we introduce GenVarFormer (GVF), a novel transformer-based architecture designed to learn mutation representations and their impact on gene expression. GVF efficiently predicts the effect of mutations up to 8 million base pairs away from a gene by only considering mutations and their local DNA context, while omitting the vast intermediate sequence. Using data from 864 breast cancer samples from The Cancer Genome Atlas, we demonstrate that GVF predicts gene expression with 26-fold higher correlation across samples than current models. In addition, GVF is the first model of its kind to generalize to unseen genes and samples simultaneously. Finally, we find that GVF patient embeddings are more informative than ground-truth gene expression for predicting overall patient survival in the most prevalent breast cancer subtype, luminal A. GVF embeddings and gene expression yielded concordance indices of $0.706^{\pm0.136}$ and $0.573^{\pm0.234}$, respectively. Our work establishes a new state-of-the-art for modeling the functional impact of non-coding mutations in cancer and provides a powerful new tool for identifying potential driver events and prognostic biomarkers.

q-bio.GN↗
arXiv2025

Building the EHR Foundation Model via Next Event Prediction

Electronic Health Records (EHRs) contain rich temporal dynamics that conventional encoding approaches fail to adequately capture. While Large Language Models (LLMs) show promise for EHR modeling, they struggle to reason about sequential clinical events and temporal dependencies. We propose Next Event Prediction (NEP), a framework that enhances LLMs' temporal reasoning through autoregressive fine-tuning on clinical event sequences. By reformulating EHRs as timestamped event chains and predicting future medical events, NEP explicitly models disease progression patterns and causal relationships. Extensive evaluations across oncology survival prediction and clinical diagnosis tasks demonstrate NEP's superiority, outperforming specialized EHR models by 4.6% AUROC and general-purpose LLMs by 7.2% C-index in temporal reasoning tasks. Our analyses reveal dual benefits: state-of-the-art prediction accuracy combined with clinically interpretable attention patterns that align with known disease pathways.

cs.AI↗
arXiv2025

Patient-specific Biomolecular Instruction Tuning

Proteomics data is essential to pathogenic understanding of a disease phenotype. In cancer, analysis of molecular signatures enables precision medicine through the identification of biological processes that drive individualized tumor progression, therapeutic resistance, and clinical heterogeneity. Recent advances in multimodal large language models (LLMs) have shown remarkable capacity to integrate and reason across heterogeneous data modalities. However, performing multi-modal language modeling for molecular understanding of patient-specific proteomics remains a significant challenge due to two barriers: (1) the lack of instruction-tuning datasets that enable clinical interpretation from proteomics data, and (2) the absence of language modeling architectures designed to capture the rich heterogeneity of molecular data. In this work, we introduce CPTAC-PROTSTRUCT, the first instruction tuning dataset for molecular understanding of oncology, comprising over 400k open-ended examples derived from individualized proteomic profiles curated from the largest national proteomics cancer study (CPTAC). Additionally, we propose KRONOS (Knowledge Representation of patient Omics Networks in Oncology via Structured tuning), a novel graph-LLM framework that leverages molecular interaction topology with proteomics to learn patient-specific graph representations for enhanced clinical reasoning. We show that KRONOS achieves competitive performance across benchmark clinical tasks, including molecular classification, temporal trajectory modeling, and tumor stage prediction from proteomics data. Ultimately, this approach empowers LLMs to understand patient-level pathogenesis, advancing precision medicine through more accurate diagnosis, prognosis, and treatment stratification.

q-bio.QM↗