Interpreting genomic variants from cancer sequencing data is a critical yet complex task in precision oncology. With advances in large language models (LLMs), there is increasing interest in leveraging their capacity for variant classification. This study benchmarks three state-of-the-art LLMs - GPT-4o, LLaMA 3, and Qwen 2.5 - on curated cancer variant databases to assess their utility in clinical genomic interpretation.
Lin et al. (Thu,) studied this question.