Susan Paul

I focus on accurate NGS data analysis and clinical interpretation, turning variant findings into clear, actionable diagnostic insights. In oncology and hereditary panel testing, I support somatic and germline variant analysis and help ensure results are grounded in evidence.

I prepare clinical reports aligned with ACMG/AMP and CAP standards (including CAP/CLIA compliance), and I review and summarize scientific literature to support robust variant classification. I also collaborate with multidisciplinary teams to integrate genomic insights into patient care and therapeutic decisions.

Across my roles as Senior Genome Analyst and Consultant Genome Analyst, I’ve led and managed genome analyst workflows, strengthened quality control, and improved efficiency. I’ve also developed SOPs for consistency and regulatory compliance, designed training programs for junior analysts, and contributed scientific updates for clinician-facing decision-making.

Before moving fully into clinical genomics operations, I worked as a biocurator reviewing cancer genomics publications and maintaining internal variant and knowledge databases. I bring a quality-driven mindset and a strong interest in leveraging AI and computational approaches to advance precision diagnostics and translational research.