Craig Myles

Craig Myles, Patrick Schrempf, David Harris-Birtill

Errors in medical text can cause delays or even result in incorrect treatment for patients. Recently, language models have shown promise in their ability to automatically detect errors in medical text, an ability that has the opportunity to significantly benefit healthcare systems. In this paper, we explore the importance of prompt optimisation for small and large language models when applied to the task of error detection. We perform rigorous experiments and analysis across frontier language models and open-source language models. We show that automatic prompt optimisation with Genetic-Pareto (GEPA) improves error detection over the baseline accuracy performance from 0.669 to 0.785 with GPT-5 and 0.578 to 0.690 with Qwen3-32B, approaching the performance of medical doctors and achieving state-of-the-art performance on the MEDEC benchmark dataset. Code available on GitHub: https://github.com/CraigMyles/clinical-note-error-detection

Craig Myles, In Hwa Um, Craig Marshall et al.

Cancer remains one of the leading causes of morbidity and mortality worldwide. Comprehensive datasets that combine histopathological images with genetic and survival data across various tumour sites are essential for advancing computational pathology and personalised medicine. We present SurGen, a dataset comprising 1,020 H&E-stained whole-slide images (WSIs) from 843 colorectal cancer cases. The dataset includes detailed annotations for key genetic mutations (KRAS, NRAS, BRAF) and mismatch repair status, as well as survival data for 426 cases. We illustrate SurGen's utility with a proof-of-concept model that predicts mismatch repair status directly from WSIs, achieving a test area under the receiver operating characteristic curve of 0.8273. These preliminary results underscore the dataset's potential to facilitate research in biomarker discovery, prognostic modelling, and advanced machine learning applications in colorectal cancer and beyond. SurGen offers a valuable resource for the scientific community, enabling studies that require high-quality WSIs linked with comprehensive clinical and genetic information on colorectal cancer. Our initial findings affirm the dataset's capacity to advance diagnostic precision and foster the development of personalised treatment strategies in colorectal oncology. Data available online: https://doi.org/10.6019/S-BIAD1285.