Join this webinar to discover how Franklin by QIAGEN streamlines the entire rapid genome analysis workflow, helping laboratories move from raw sequencing data to clinically actionable reports in record time. Through a live demonstration, you'll see how Franklin combines AI-assisted variant prioritization, automated ACMG classification, phenotype-driven analysis and integrated clinical evidence to reduce millions of variants to a concise list of the most relevant findings.

Reduce turnaround time with an end-to-end, automated rapid genome workflow

Prioritize clinically relevant variants using AI-assistance and phenotype-driven analysis

Standardize interpretation with automated ACMG classification and reusable internal knowledge

Leverage more than 100 integrated databases alongside Franklin's unique community knowledge base

Scale confidently across sequencing platforms, variant types and laboratory workflows with a vendor-agnostic solution

Simplify variant filtering, collaborative review and report generation with highly customizable workflows