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Franklin - The Future of Variant Interpretation. The most advanced way for variant classification, a FREE comprehensive interpretation tool by Genoox. Try it - search any variant.
Franklin allows genomic professionals to spend less time pinpointing evidence, and more time drilling down into insights and actionability. We are building the largest, most diverse real-world evidence dataset – answering any genomic question through the power of the community, data and insights.
Franklin - The Future of Variant Interpretation. The most advanced way for variant classification, a FREE comprehensive interpretation tool by Genoox. Try it - search any variant.
The Genoox Technology. Our indication agnostic data platform delivers accurate insights driven by our community of clinical users, Franklin. The real-world evidence we produce enhances clinical decision-making, fine-tunes care pathways and enables more targeted therapies. Learn More.
Interpreting CNVs Check out this quick guide of Franklin's Variant Interpretation hub for structural variants. Editing segments Learn how to use Franklin's powerful visualization tools to modify the edges of your structural variants. Clinical evidence for SV.
Welcome to Franklin by Genoox! The purpose of this guide is to help you take your first steps using Franklin.
Franklin's AI-based classification engine adheres to ACMG/AMP standards and guidelines. Additionally, it integrates supplementary knowledge from databases and literature to expedite gene-specific variant classification.
Franklin - The Future of Variant Interpretation. The most advanced way for variant classification, a FREE comprehensive interpretation tool by Genoox. Try it - search any variant.
Franklin for WGS solution is an end-to-end suite of tools that help you sharpen single and family case analysis by combining AI technology with the richest genetic data available for simple SNPs and complex variants such as CNVs, ROHs, mitochondrial, and even short tandem repeats.
Franklin for WES solution is an end-to-end suite of tools that help you sharpen single and family case analysis by combining AI technology with the richest genetic data available for SNPs, CNVs, ROHs, and even mitochondrial variants.
