RareBench Can LLMs Serve as Rare Diseases Specialists?

🤗 HF Repo • 📃 Paper

RareBench is a pioneering benchmark designed to systematically evaluate the capabilities of LLMs on 4 critical dimensions within the realm of rare diseases. Meanwhile, we have compiled the largest open-source dataset on rare disease patients, establishing a benchmark for future studies in this domain. To facilitate differential diagnosis of rare diseases, we develop a dynamic few-shot prompt methodology, leveraging a comprehensive rare disease knowledge graph synthesized from multiple knowledge bases, significantly enhancing LLMs’ diagnos- tic performance. Moreover, we present an exhaustive comparative study of GPT-4’s diagnostic capabilities against those of specialist physicians. Our experimental findings underscore the promising potential of integrating LLMs into the clinical diagnostic process for rare diseases.

⚙️ How to evaluate on LongBench

Load Data

from datasets import load_dataset

datasets = ["RAMEDIS", "MME", "HMS", "LIRICAL", "PUMCH_ADM"]

for dataset in datasets:
    data = load_dataset('chenxz/RareBench', dataset, split='test')
    print(data)

API-based LLMs

Put your own Openai key in the llm_utils/gpt_key.txt file.
Put your own Gemini key in the llm_utils/gemini_key.txt file.
Put your own Zhipuai key in the llm_utils/glm_key.txt file.

Local LLMs

Replace the content in the mapping/local_llm_path.json file with the path to the LLM on your local machine.

📄 Acknowledgement

• Some of the dataset of RareBench are based on previous researchers, including RAMEDIS, MME, LIRICAL PhenoBrain.

📝 Citation

@article{chen2024rarebench,
  title={RareBench: Can LLMs Serve as Rare Diseases Specialists?},
  author={Chen, Xuanzhong and Mao, Xiaohao and Guo, Qihan and Wang, Lun and Zhang, Shuyang and Chen, Ting},
  journal={arXiv preprint arXiv:2402.06341},
  year={2024}
}