Brad Chapman

This paper demonstrates an LLM-driven autonomous lab that reduces the cost of cell-free protein synthesis by 40% and increases titer by 27% through iterative optimization.

The paper develops standardized tools and best practices for benchmarking germline small variant calls in human genomes using truth sets and performance metrics.

Bioconda provides a sustainable, comprehensive distribution of bioinformatics software using Conda for reproducible analysis across platforms.

The paper introduces a tiered prioritisation approach to identify high-impact gene fusions in cancer genomes by improving variant annotation, interpretation, and visualisation.