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Qiang Ju

Qiang Ju contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

Do We Really Need External Tools to Mitigate Hallucinations? SIRA: Shared-Prefix Internal Reconstruction of Attribution

Large vision-language models (LVLMs) often hallucinate when language priors dominate weak or ambiguous visual evidence. Existing contrastive decoding methods mitigate this problem by comparing predictions from the original image with those from externally perturbed visual inputs, but such references can introduce off-manifold artifacts and require costly extra forward passes. We propose SIRA, a training-free internal contrastive decoding framework that constructs a counterfactual reference inside the same LVLM by exploiting the staged information flow of multimodal transformers. Instead of removing visual information from the input, SIRA first lets image and text tokens interact through a shared prefix, forming an aligned multimodal state that preserves prompt interpretation, decoding history, positional structure, and early visual grounding. It then forks a counterfactual branch in later transformer layers, where attention to image-token positions is masked. This branch retains the shared multimodal context but lacks continued access to fine-grained visual evidence, yielding a language-prior-dominated internal reference for token-level contrast. During decoding, SIRA suppresses tokens that remain strong without late visual access and favors predictions whose advantage depends on the full visual pathway. Experiments on POPE, CHAIR, and AMBER with Qwen2.5-VL and LLaVA-v1.5 show that SIRA consistently reduces hallucinations while preserving descriptive coverage and incurring lower overhead than two-pass contrastive decoding. SIRA requires no training, external verifier, or perturbed input, and applies to open-weight LVLMs with white-box inference access.

preprint2026arXiv

SkinFlow: Efficient Information Transmission for Open Dermatological Diagnosis via Dynamic Visual Encoding and Staged RL

General-purpose Large Vision-Language Models (LVLMs), despite their massive scale, often falter in dermatology due to "diffuse attention" - the inability to disentangle subtle pathological lesions from background noise. In this paper, we challenge the assumption that parameter scaling is the only path to medical precision. We introduce SkinFlow, a framework that treats diagnosis as an optimization of visual information transmission efficiency. Our approach utilizes a Virtual-Width Dynamic Vision Encoder (DVE) to "unfold" complex pathological manifolds without physical parameter expansion, coupled with a two-stage Reinforcement Learning strategy. This strategy sequentially aligns explicit medical descriptions (Stage I) and reconstructs implicit diagnostic textures (Stage II) within a constrained semantic space. Furthermore, we propose a clinically grounded evaluation protocol that prioritizes diagnostic safety and hierarchical relevance over rigid label matching. Empirical results are compelling: our 7B model establishes a new state-of-the-art on the Fitzpatrick17k benchmark, achieving a +12.06% gain in Top-1 accuracy and a +28.57% boost in Top-6 accuracy over the massive general-purpose models (e.g., Qwen3VL-235B and GPT-5.2). These findings demonstrate that optimizing geometric capacity and information flow yields superior diagnostic reasoning compared to raw parameter scaling.