Abstract:Scientific compound figures combine multiple labeled panels into a single image, but captions in real pipelines are often missing or only provide figure-level summaries, making panel-level understanding difficult. In this paper, we propose FigEx2, visual-conditioned framework that localizes panels and generates panel-wise captions directly from the compound figure. To mitigate the impact of diverse phrasing in open-ended captioning, we introduce a noise-aware gated fusion module that adaptively filters token-level features to stabilize the detection query space. Furthermore, we employ a staged optimization strategy combining supervised learning with reinforcement learning (RL), utilizing CLIP-based alignment and BERTScore-based semantic rewards to enforce strict multimodal consistency. To support high-quality supervision, we curate BioSci-Fig-Cap, a refined benchmark for panel-level grounding, alongside cross-disciplinary test suites in physics and chemistry. Experimental results demonstrate that FigEx2 achieves a superior 0.726 mAP@0.5:0.95 for detection and significantly outperforms Qwen3-VL-8B by 0.51 in METEOR and 0.24 in BERTScore. Notably, FigEx2 exhibits remarkable zero-shot transferability to out-of-distribution scientific domains without any fine-tuning.
Abstract:Multimodal Large Language Models (MLLMs) have shown strong potential for radiology report generation, yet their clinical translation is hindered by architectural heterogeneity and the prevalence of factual hallucinations. Standard supervised fine-tuning often fails to strictly align linguistic outputs with visual evidence, while existing reinforcement learning approaches struggle with either prohibitive computational costs or limited exploration. To address these challenges, we propose a comprehensive framework for self-consistent radiology report generation. First, we conduct a systematic evaluation to identify optimal vision encoder and LLM backbone configurations for medical imaging. Building on this foundation, we introduce a novel "Reason-then-Summarize" architecture optimized via Group Relative Policy Optimization (GRPO). This framework restructures generation into two distinct components: a think block for detailed findings and an answer block for structured disease labels. By utilizing a multi-dimensional composite reward function, we explicitly penalize logical discrepancies between the generated narrative and the final diagnosis. Extensive experiments on the MIMIC-CXR benchmark demonstrate that our method achieves state-of-the-art performance in clinical efficacy metrics and significantly reduces hallucinations compared to strong supervised baselines.
Abstract:Sparse activation, which selectively activates only an input-dependent set of neurons in inference, is a useful technique to reduce the computing cost of Large Language Models (LLMs) without retraining or adaptation efforts. However, whether it can be applied to the recently emerging Small Language Models (SLMs) remains questionable, because SLMs are generally less over-parameterized than LLMs. In this paper, we aim to achieve sparse activation in SLMs. We first show that the existing sparse activation schemes in LLMs that build on neurons' output magnitudes cannot be applied to SLMs, and activating neurons based on their attribution scores is a better alternative. Further, we demonstrated and quantified the large errors of existing attribution metrics when being used for sparse activation, due to the interdependency among attribution scores of neurons across different layers. Based on these observations, we proposed a new attribution metric that can provably correct such errors and achieve precise sparse activation. Experiments over multiple popular SLMs and datasets show that our approach can achieve 80% sparsification ratio with <5% model accuracy loss, comparable to the sparse activation achieved in LLMs. The source code is available at: https://github.com/pittisl/Sparse-Activation.