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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 - 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.
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.
Dive into the intricacies of tumor profiling with a comprehensive session led by Franklin's experts, providing both an introduction and a detailed demonstration. At Franklin Webinars, we are committed to advancing genomic education and supporting the professional development of our community.
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.
Welcome to Franklin by Genoox! The purpose of this guide is to help you take your first steps using Franklin.
That’s why we created Franklin (Genoox’s community platform), the world’s first professional genomic community of users. Together with Genoox’s learning system, the Franklin community is bridging the gap between publicly-available data and real world 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
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.
