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1. franklin.genoox.comFranklin

   franklin.genoox.com

   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.

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     Knowledge Base - Franklin

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     Our Products and Services include our analytic tools and...

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     Franklin - Franklin

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   • Franklin Variant Interpretation Hub

     Interpreting CNVs Check out this quick guide of Franklin's...

   • Explore variants data in Franklin

     Explore variants data in Franklin. Written by Assaf Sheffer....

2. help.genoox.com › en › collectionsFranklin Variant Interpretation Hub | Franklin Help Center

   help.genoox.com › en › collections

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   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.

3. wustl.genoox.com › analysis-toolFranklin - Genoox

   wustl.genoox.com › analysis-tool

   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.

4. help.genoox.com › en › articlesExplore variants data in Franklin | Franklin Help Center - Genoox

   help.genoox.com › en › articles

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   Learn how to use the variant search and interpretation hub features in Franklin, a tool for analyzing genetic variants. Find examples, annotations, and updates for SNP, SV, and ROH variants.

5. lp.genoox.com › workflows › wgsFranklin for Whole Genome Sequencing (WGS)

   lp.genoox.com › workflows › wgs

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   Franklin is a platform that helps you analyze WGS data for single and family cases, using AI and rich genetic data. It supports variant detection, interpretation, reporting, and collaboration with the Franklin Community.

6. help.genoox.com › en › collectionsHow to start using Franklin | Franklin Help Center - Genoox

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   Explore variants data in Franklin. Welcome to Franklin by Genoox! The purpose of this guide is to help you take your first steps using Franklin.

7. People also ask

   How many variants does Franklin provide?

   • Franklin presents information from more than 100 variants according to the latest ACMG guidelines. The platform team of genetics specialists. potentially causal variants. This comprehensive tool allows zygosity, and more. historical data. Working side by side with colleagues?

   Franklin for Whole Exome Sequencing (WES) - Genoox

   lp.genoox.com/workflows/wes

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   What types of genomic variants is Franklin able to call?

   • Franklin is also able to call other complex genomic variants such as deep complex indels, mitochondrial variants, and short tandem repeats, and present them in wonderful visualizations using the Whole-Genome viewer. publications. Franklin presents information from more than 100

   Franklin for Whole Genome Sequencing (WGS)

   lp.genoox.com/workflows/wgs

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   What do I need to know about Franklin's interpretation engine?

   • Everything you need to know about Franklin's interpretation engine. CNV Variant Assessment tab Discover Franklin's CNV Variant Assessment tab—a powerful tool that provides comprehensive insights into genomic regions. Interpreting CNVs Check out this quick guide of Franklin's Variant Interpretation hub for structural variants.

   Franklin Variant Interpretation Hub | Franklin Help Center - Genoox

   help.genoox.com/en/collections/2077313-franklin-variant-interpretation-hub

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   What is Franklin for WGS?

   • 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. Get started now!

   Franklin for Whole Genome Sequencing (WGS)

   lp.genoox.com/workflows/wgs

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8. lp.genoox.com › workflows › wesFranklin for Whole Exome Sequencing (WES) - Genoox

   lp.genoox.com › workflows › wes

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   Franklin is a platform that helps you analyze WES data from SNPs, CNVs, ROHs, and mitochondrial variants. It uses AI, machine learning, and rich genetic data to streamline your case analysis from FASTQ to report.