I work across cancer genomics, gene therapy, proteomics, and single-cell biology, building reproducible workflows that turn complex omics data into clear, useful answers.
Clear analysis. Reproducible workflows. Results teams can use.
Engineered production-grade Nextflow workflows for 20+ TB of Genomics England WGS data within a secure clinical research environment.
Automated clinical reporting workflows integrating variant calls and participant metadata, reducing turnaround to under 3 hours.
Led bioinformatics delivery for a €4M European work package, coordinating 30+ researchers and partner sites across gene therapy and oncology projects.
Built single-cell and NGS workflows, standardizing QC and cross-site harmonization for translational and clinical-stage studies.
Administered and optimized a 7-node HPC cluster, supporting reproducible multi-user analysis with 99% compute availability.
Harmonized scMultiome datasets across XPAND clinical sites to support cross-centre comparison and downstream translational analysis.
Validated LT-HSC signatures in AML-derived cells, linking multi-omic profiles to clinically relevant cell-state interpretation.
Designed Snakemake preprocessing workflows for large-scale NGS datasets, reducing turnaround time and standardizing execution.
Built relational databases to centralize experimental metadata and strengthen data integrity across collaborative projects.
Optimized LC-MS and quantitative proteomics workflows, reducing turnaround time by 1.5 days and increasing sample throughput.
Developed traceability analytics for industrial quality control, translating experimental data into cost-saving decisions.
Secure WGS workflow for germline predisposition analysis in AML, built to support fast and interpretable reporting in the Genomics England environment.
Automated single-cell workflow that takes raw counts to interpretable results through reproducible analysis and a simple interactive dashboard.
Reproducible bulk RNA-seq workflow for differential expression, pathway analysis, and self-contained reporting.
Open-source R package for clean single-cell visualizations and faster, more consistent figure generation.
Hackathon prototype for adding traceability and context to electronic lab notebooks without changing existing workflows.
I started in the wet lab, working in proteomics and seeing first-hand how much biological value can stay hidden inside complex datasets. That was the turning point that pulled me into bioinformatics. Since then, I have spent more than a decade across genomics and computational biology, building a profile that combines scientific intuition with the discipline to make analysis reproducible, scalable, and genuinely useful.
Today, I develop bioinformatic solutions for translational and biomedical research across multi-omics, gene therapy, cancer genomics, and workflow engineering. I build in Nextflow and Snakemake, support HPC environments, and work with researchers, clinicians, and technical teams to turn raw data into decisions and usable workflows.
In industry, good bioinformatics is not just about getting analyses to run. It is about building work that is reliable, maintainable, and scalable when quality and clinical impact matter. That is why traceability is important to me, and why ISO 13485 internal auditor certification and IEC 62304-informed practices already shape how I approach development.
Good bioinformatics should be clear,
reproducible, and useful.
If that is what your team needs, I would be glad to talk.