I’m Salvatore Barbagallo, a bioinformatics and computational genomics professional based in London with 7+ years of experience across clinical genomics and regulated environments. I build reproducible, scalable NGS workflows—especially RNA-seq and variant analysis pipelines—using Python, R, Bash, SQL, and workflow tooling like Nextflow and Docker, with a strong focus on data quality, automation, and reliability. Across my roles, I’ve worked end-to-end from sample- and trial-support operations to production-grade analytics: designing automation tools to reduce reconciliation errors, supporting multiple clinical/ATMP trials, and developing robust pipelines for differential expression and WGS drug-resistance mutation analysis. I enjoy bridging lab realities with computational engineering so analyses are decision-ready, traceable, and built for trustworthy downstream use.…I’m Salvatore Barbagallo, a bioinformatics and computational genomics professional based in London with 7+ years of experience across clinical genomics and regulated environments. I build reproducible, scalable NGS workflows—especially RNA-seq and variant analysis pipelines—using Python, R, Bash, SQL, and workflow tooling like Nextflow and Docker, with a strong focus on data quality, automation, and reliability. Across my roles, I’ve worked end-to-end from sample- and trial-support operations to production-grade analytics: designing automation tools to reduce reconciliation errors, supporting multiple clinical/ATMP trials, and developing robust pipelines for differential expression and WGS drug-resistance mutation analysis. I enjoy bridging lab realities with computational engineering so analyses are decision-ready, traceable, and built for trustworthy downstream use.WWWW…