Summary
Barry Moore is a Senior Scientist for Precision Genomics with over 25 years at the intersection of bench biology, bioinformatics, and clinical translation, now focused on clinical-grade, AI-driven genome interpretation. He has led development and applied use of foundational tools like MAKER, VAAST, and VVP, designed diagnostic workflows for programs such as NeoSeq and Heritage 1K, and long partnered with Fabric Genomics to refine the GEM interpretation engine. Known as the person teams call when “something must work,” he blends domain depth in variant prioritization, ontology-driven phenotype profiling, and scalable consortia workflows with practical engineering across clinical and research settings. Based in Salt Lake City, he brings rare-disease diagnostic impact, mentorship experience, and a consistent track record of turning genomic advances into production-ready tools.
16 years of coding experience
16 years of employment as a software developer
MS, Biology, MS, Biology at Loma Linda University
B.S., Chemisty, Biology, B.S., Chemisty, Biology at Southwestern Adventist University