arXiv subjects

Hongwang Xiao

Publications and source records attributed to Hongwang Xiao.

4 recordsLinked to original sources

arXiv2026

AREX: Towards a Recursively Self-Improving Agent for Deep Research

Deep research requires agents to find answers that jointly satisfy multiple constraints. Discovering such answers is costly, whereas verifying a candidate can often be decomposed into tractable constraint-wise checks. This discovery--verification asymmetry suggests that a research agent should do more than simply search longer: it should recursively improve its current answer by verifying intermediate results and using the partially verified state to guide subsequent refinement. We introduce AREX, a family of Recursively Self-Improving (RSI) deep research agents. AREX alternates between an inner research loop that gathers evidence and constructs a provisional answer, and an outer self-improvement loop that audits the answer constraint-wise, identifies unresolved claims, and launches targeted follow-up research. To sustain RSI over long horizons, AREX learns an autonomous context-update tool that compresses growing interaction history into a compact improvement state preserving verified evidence and unresolved constraints, without relying on an external model. We train AREX on verified synthetic tasks and high-quality trajectories through agentic mid-training and long-horizon reinforcement learning. To mitigate sparse final rewards during long horizon learning, we emphasize key steps where decisive evidence is acquired or erroneous research directions are corrected. We instantiate a dense 4B model and a 122B-A10B Mixture-of-Experts model. Across BrowseComp, WideSearch, DeepSearchQA, Humanity's Last Exam (HLE), and other reasoning and tool-use benchmarks, AREX substantially outperforms comparable-scale baselines and remains competitive with models using substantially more activated parameters.

cs.AI↗

arXiv2026

Towards Unified Multi-task EEG Analysis with Low-Rank Adaptation

Recent self-supervised pre-training methods for electroencephalogram (EEG) have shown promising results. However, the pre-trained models typically require full fine-tuning on each downstream task individually to achieve good performance. In practical applications involving multiple tasks, utilizing a separate model for each task is not ideal regarding computational and spatial cost. In this study, we go one step further and explore the simultaneous adaptation of a pre-trained model to multiple different tasks. The EEG signals exhibit significant heterogeneity due to their collection from various subjects using diverse devices and experimental setups, resulting in potential conflicts among different tasks that impede joint optimization. To tackle this challenge, we propose MTEEG, a multi-task EEG analysis framework which incorporates task-specific low-rank adaptation (LoRA) modules to disentangle the parameter space and alleviate task conflicts. To investigate the trade-off between task specification and interaction, we propose three variants of MTEEG that integrate the LoRA modules in different ways and evaluate them on six downstream tasks, demonstrating that MTEEG can surpass state-of-the-art single-task methods on the majority of metrics. MTEEG shows the potential of multi-task EEG analysis and promotes the development of general-purpose brain-computer interfaces in the future.

cs.LG↗

arXiv2026

Autoregressive Visual Decoding from EEG Signals

Electroencephalogram (EEG) signals have become a popular medium for decoding visual information due to their cost-effectiveness and high temporal resolution. However, current approaches face significant challenges in bridging the modality gap between EEG and image data. These methods typically rely on complex adaptation processes involving multiple stages, making it hard to maintain consistency and manage compounding errors. Furthermore, the computational overhead imposed by large-scale diffusion models limit their practicality in real-world brain-computer interface (BCI) applications. In this work, we present AVDE, a lightweight and efficient framework for visual decoding from EEG signals. First, we leverage LaBraM, a pre-trained EEG model, and fine-tune it via contrastive learning to align EEG and image representations. Second, we adopt an autoregressive generative framework based on a "next-scale prediction" strategy: images are encoded into multi-scale token maps using a pre-trained VQ-VAE, and a transformer is trained to autoregressively predict finer-scale tokens starting from EEG embeddings as the coarsest representation. This design enables coherent generation while preserving a direct connection between the input EEG signals and the reconstructed images. Experiments on two datasets show that AVDE outperforms previous state-of-the-art methods in both image retrieval and reconstruction tasks, while using only 10% of the parameters. In addition, visualization of intermediate outputs shows that the generative process of AVDE reflects the hierarchical nature of human visual perception. These results highlight the potential of autoregressive models as efficient and interpretable tools for practical BCI applications.

cs.LG↗

arXiv2025

STELLA: A Multimodal LLM for Protein Functional Annotation via Unified Sequence-Structure Encoding

Understanding the intricate interplay among sequence, structure, and function remains a fundamental challenge in proteomics. The sequence-structure-function paradigm posits that biological roles are governed by the tertiary geometric conformations encoded within primary sequences; consequently, integrating these multi-modal descriptors is imperative for accurate functional annotation. While protein language models (pLMs) have achieved significant progress via representation learning on massive sequence data, they often lack the capacity to incorporate high-resolution structural information and the rich textual context that characterizes protein roles. In this work, we present STELLA, a multimodal LLM that synergistically aligns bimodal (sequence-structure) representations with the textual modality to advance protein functional annotation. By leveraging ESM3 for unified bimodal encoding and Llama-3.1-8B-Instruct for natural language modeling, STELLA achieves state-of-the-art performance in two critical tasks: Functional Description Prediction and Enzyme-catalyzed Reaction Prediction. This study demonstrates that multimodal LLMs represent a paradigm shift beyond pure pLMs, offering a new frontier for protein biology and biomedical discovery. The codes can be accessed via https://github.com/ocx-lab/STELLA.

q-bio.BM↗