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Updated: Sep 10, 2025

Augmenting Large Language Models via Vector Embeddings to Improve Domain-Specific Responsiveness
Published on: December 6, 2024
Resource-efficient instruction tuning of large language models for biomedical named entity recognition
Hui Liu1, Ziyi Chen2, Peilin Li3
1School of Biomedical Engineering, Division of Life Sciences and Medicine, University of Science and Technology of China, No. 96, JinZhai Road Baohe District, Hefei, 230026, Anhui, China; Suzhou Institute for Advanced Research, University of Science and Technology of China, No. 166, Renai Road, Suzhou, 215123, Jiangsu, China; Department of Precision Machinery and Precision Instruments, University of Science and Technology of China, No. 96, JinZhai Road Baohe District, Hefei, 230026, Anhui, China.
Parameter-efficient fine-tuning (PEFT) optimizes large language models (LLMs) for biomedical named entity recognition (BioNER) with fewer resources. The resulting NERLlama3.1 model achieves high performance and strong generalization, outperforming fully fine-tuned models.
Area of Science:
- Biomedical Natural Language Processing
- Artificial Intelligence
- Computational Linguistics
Background:
- Large language models (LLMs) show promise for biomedical named entity recognition (BioNER).
- Fine-tuning LLMs for BioNER demands significant computational resources, limiting accessibility.
- Parameter-efficient fine-tuning (PEFT) offers a solution for resource-constrained environments.
Purpose of the Study:
- Investigate PEFT techniques for optimizing LLMs in BioNER under limited computational conditions.
- Maintain competitive model performance and in-domain generalization capability.
- Explore multi-task BioNER capabilities of fine-tuned LLMs.
Main Methods:
- Utilized QLoRA, a PEFT method, to fine-tune the Llama3.1 model for BioNER, creating NERLlama3.1.
- Developed an LLM instruction tuning dataset using existing BioNER datasets (NCBI-disease, BC5CDR-chem, BC2GM-gene).
- Fine-tuned Llama3.1-8B on a single 16GB GPU and incorporated self-consistency NER prompting (SCNP) during inference.
Main Results:
- NERLlama3.1 achieved high F1-scores: 0.8977 (NCBI-disease), 0.9402 (BC5CDR-chemical), 0.8530 (BC2GM-gene).
- Demonstrated strong generalization on unseen datasets (e.g., 0.8378 on NLM-gene).
- Outperformed fully fine-tuned LLMs and BERT-base in BioNER tasks, showing superior in-domain generalization.
Conclusions:
- NERLlama3.1, using PEFT, achieved high BioNER performance with significantly reduced computational requirements.
- The model exhibits superior in-domain generalization compared to traditional pre-trained models.
- Low resource demands, high performance, and strong generalization make NERLlama3.1 suitable for diverse clinical BioNER applications.
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