cs.AI updates on arXiv.org 08月14日
Leveraging Large Language Models for Rare Disease Named Entity Recognition
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本文评估了GPT-4o在罕见病命名实体识别(NER)中的能力,通过多种提示策略和结构化提示框架,在低资源环境下实现了与BioClinicalBERT相当或更优的性能。

arXiv:2508.09323v1 Announce Type: cross Abstract: Named Entity Recognition (NER) in the rare disease domain poses unique challenges due to limited labeled data, semantic ambiguity between entity types, and long-tail distributions. In this study, we evaluate the capabilities of GPT-4o for rare disease NER under low-resource settings, using a range of prompt-based strategies including zero-shot prompting, few-shot in-context learning, retrieval-augmented generation (RAG), and task-level fine-tuning. We design a structured prompting framework that encodes domain-specific knowledge and disambiguation rules for four entity types. We further introduce two semantically guided few-shot example selection methods to improve in-context performance while reducing labeling effort. Experiments on the RareDis Corpus show that GPT-4o achieves competitive or superior performance compared to BioClinicalBERT, with task-level fine-tuning yielding new state-of-the-art (SOTA) results. Cost-performance analysis reveals that few-shot prompting delivers high returns at low token budgets, while RAG offers marginal additional benefit. An error taxonomy highlights common failure modes such as boundary drift and type confusion, suggesting opportunities for post-processing and hybrid refinement. Our results demonstrate that prompt-optimized LLMs can serve as effective, scalable alternatives to traditional supervised models in biomedical NER, particularly in rare disease applications where annotated data is scarce.

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GPT-4o 命名实体识别 罕见病 低资源环境
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