Summary
Bruce Moran is a bioinformatics specialist with 10 years' experience applying sequencing and genomic analysis to cancer diagnosis and research, currently based at St. Vincent’s University Hospital in Dublin. He combines a PhD in statistics and bioinformatics with hands-on expertise in exome and transcriptome analysis, NGS workflows, and diagnostic panel interpretation developed across academia and industry. His background spans postdoctoral cancer genomics, development of the OncoMasTR panel, and early work in population genetics and Sanger sequencing, giving him a rare blend of clinical and research sequencing perspectives. Known for turning complex sequencing datasets into clinically actionable insights, he pairs statistical rigor with practical pipeline implementation and a focus on translational impact.
10 years of coding experience
3 years of employment as a software developer
MSc. (taught) Quantitative Genetics and Genome Analysis, QGEN, Pass, MSc. (taught) Quantitative Genetics and Genome Analysis, QGEN, Pass at The University of Edinburgh
Doctor of Philosophy, Statistics, bioinformatics, NGS data analysis., Doctor of Philosophy, Statistics, bioinformatics, NGS data analysis. at University College Dublin
perl, r, bash, sql