Zimo Zhao

Bowen Yu, Maolin Wang, Sheng Zhang et al.

Distilling Chain-of-Thought (CoT) reasoning from large language models into compact student models presents a fundamental challenge: teacher rationales are often too verbose for smaller models to faithfully reproduce. Existing approaches either compress reasoning into single-step, losing the interpretability that makes CoT valuable. We present a three-stage curriculum learning framework that addresses this capacity mismatch through progressive skill acquisition. First, we establish structural understanding via masked shuffled reconstruction. Second, we apply Group Relative Policy Optimization (GRPO) on masked completion tasks, enabling the model to discover its own balance between accuracy and brevity. Third, we identify persistent failure cases and guide the student to internalize teacher knowledge through targeted rewriting, again optimized with GRPO. Experiments on GSM8K demonstrate that our approach enables Qwen2.5-3B-Base to achieve an 11.29 percent accuracy improvement while reducing output length by 27.4 percent, surpassing both instruction-tuned variants and prior distillation methods.

Qiming He, Jing Li, Tian Guan et al.

Glomerular pathology is central to the diagnosis and prognosis of renal diseases, yet the heterogeneity of glomerular morphology and fine-grained lesion patterns remain challenging for current AI approaches. We present GloPath, an entity-centric foundation model trained on over one million glomeruli extracted from 14,049 renal biopsy specimens using multi-scale and multi-view self-supervised learning. GloPath addresses two major challenges in nephropathology: glomerular lesion assessment and clinicopathological insights discovery. For lesion assessment, GloPath was benchmarked across three independent cohorts on 52 tasks, including lesion recognition, grading, few-shot classification, and cross-modality diagnosis-outperforming state-of-the-art methods in 42 tasks (80.8%). In the large-scale real-world study, it achieved an ROC-AUC of 91.51% for lesion recognition, demonstrating strong robustness in routine clinical settings. For clinicopathological insights, GloPath systematically revealed statistically significant associations between glomerular morphological parameters and clinical indicators across 224 morphology-clinical variable pairs, demonstrating its capacity to connect tissue-level pathology with patient-level outcomes. Together, these results position GloPath as a scalable and interpretable platform for glomerular lesion assessment and clinicopathological discovery, representing a step toward clinically translatable AI in renal pathology.

Xiao Han, Zimo Zhao, Wanyu Wang et al.

Recent advancements in Large Language Models (LLMs) have emphasized the critical role of fine-tuning (FT) techniques in adapting LLMs to specific tasks, especially when retraining from scratch is computationally infeasible. Fine-tuning enables LLMs to leverage task- or domain-specific data, producing models that more effectively meet the requirements of targeted applications. However, conventional FT approaches often suffer from catastrophic forgetting and suboptimal data efficiency, limiting their real-world applicability. To address these challenges, this paper proposes \textbf{DEAL}, a novel framework that integrates Low-Rank Adaptation (LoRA) with a continuous fine-tuning strategy. By incorporating knowledge retention and adaptive parameter update modules, the framework mitigates the limitations of existing FT methods while maintaining efficiency. Experiments on 15 diverse datasets show that DEAL consistently outperforms baseline methods, yielding substantial gains in task accuracy and resource efficiency. These findings demonstrate the potential of our approach to advance continual adaptation in LLMs by enhancing task performance while improving resource efficiency. The source code is publicly available at https://github.com/zzm-black/DEAL-Continuous-Low-Rank-Fine-Tuning.

Bowen Liu, Pengyue Jia, Wanyu Wang et al.

The primary objective of cross-view UAV geolocalization is to identify the exact spatial coordinates of drone-captured imagery by aligning it with extensive, geo-referenced satellite databases. Current approaches typically extract features independently from each perspective and rely on basic heuristics to compute similarity, thereby failing to explicitly capture the essential interactions between different views. To address this limitation, we introduce a novel, plug-and-play ranking architecture designed to explicitly perform joint relational modeling for improved UAV-to-satellite image matching. By harnessing the capabilities of a Large Vision-Language Model (LVLM), our framework effectively learns the deep visual-semantic correlations linking UAV and satellite imagery. Furthermore, we present a novel relational-aware loss function to optimize the training phase. By employing soft labels, this loss provides fine-grained supervision that avoids overly penalizing near-positive matches, ultimately boosting both the model's discriminative power and training stability. Comprehensive evaluations across various baseline architectures and standard benchmarks reveal that the proposed method substantially boosts the retrieval accuracy of existing models, yielding superior performance even under highly demanding conditions.

Jiawen Li, Tian Guan, Qingxin Xia et al.

Foundation models have revolutionized the paradigm of digital pathology, as they leverage general-purpose features to emulate real-world pathological practices, enabling the quantitative analysis of critical histological patterns and the dissection of cancer-specific signals. However, these static general features constrain the flexibility and pathological relevance in the ever-evolving needs of clinical applications, hindering the broad use of the current models. Here we introduce PathFiT, a dynamic feature learning method that can be effortlessly plugged into various pathology foundation models to unlock their adaptability. Meanwhile, PathFiT performs seamless implementation across diverse pathology applications regardless of downstream specificity. To validate PathFiT, we construct a digital pathology benchmark with over 20 terabytes of Internet and real-world data comprising 28 H\&E-stained tasks and 7 specialized imaging tasks including Masson's Trichrome staining and immunofluorescence images. By applying PathFiT to the representative pathology foundation models, we demonstrate state-of-the-art performance on 34 out of 35 tasks, with significant improvements on 23 tasks and outperforming by 10.20% on specialized imaging tasks. The superior performance and versatility of PathFiT open up new avenues in computational pathology.