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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.
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.
Welcome to Franklin by Genoox! The purpose of this guide is to help you take your first steps using Franklin.
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.
The Franklin platform has an advanced artificial intelligence-driven engine designed to prioritize and interpret variant data. This powerful engine extracts a range of features from diverse sources of evidence and identifies the most probable causal pathogenic variants to add them to the Workbench for the user's review.
Highlighted Pages. Watch Franklin Exclusive Webinars. How Franklin is organized. Who was Franklin? Franklin's Advanced Filtering System.
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.
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.
