My main interests revolve around making complex genomics data both manageable and meaningful. With over 15 years of experience across functional genomics and advanced sequencing analysis, I’m keen to work with research groups to understand their scientific questions and identify the most effective computational strategies to support them. My background covers a wide spectrum of omics data analyses, from rare disease genomics to transcription factor biology, microbiome and epigenomics, using both short‑ and long‑read sequencing technologies.

At LMS, I’m excited to help translate multidimensional omics datasets into actionable insights, whether for pilot studies or large-scale sequencing projects. I’m particularly focused on streamlining and automating routine workflows to free up time for more bespoke collaborative projects. Working closely with the other LMS facilities, I aim to contribute across the full lifecycle of a study, from experimental design through to data interpretation, while expanding our analytical and training offerings in line with the latest developments in the field.