RDMA equips small LLMs with abbreviation resolution, phenotype reasoning, and ontology tools to mine rare diseases from EHR notes, outperforming fine-tuned and RAG baselines at up to 10x lower inference cost.
European Journal of Public Health 30(Supplement 5), 166–494 (2020)
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RDMA: Cost Effective Agent-Driven Rare Disease Mining from Electronic Health Records
RDMA equips small LLMs with abbreviation resolution, phenotype reasoning, and ontology tools to mine rare diseases from EHR notes, outperforming fine-tuned and RAG baselines at up to 10x lower inference cost.