Genoox

Assaf Sheffer

Noga Yaffe

Liron

Everything you need to know about Franklin's interpretation engine.

Franklin Variant Interpretation Hub

Franklin suggested classification

Assessment tools overview

Variant Classification Tags

**SNP & Indel Variants

CNV Variant Assessment tab

Check out this quick guide of Franklin's Variant Interpretation hub for structural variants.

Interpreting CNVs

Learn how to use Franklin's powerful visualization tools to modify the edges of your structural variants.

Editing segments

Clinical evidence for SV

Meet Franklin Genes and regions section, where you can review the regions which your CNV intersects

CNV Genes and Regions tab

Explore the 'Associated Conditions' tab for a comprehensive view of condition-variant associations.

CNV Associated Conditions tabs

Stav nutkevitch

** CNV & ROH Variants

Meet Franklin powerful Geno-Pheno engine that collects and curated data from multiple sources to help you find the relevant condition

Variant associated conditions overview

Associated conditions

Explore Franklin's rich and comprehensive genomic literature database for SNP and CNV interpretation

Franklin's Publication engine

  Publications      

Here you can find a list of the prediction tools used by Franklin for variant  classification

Prediction tools and score range

External Sources and Databases

Discover new evidence shared by Franklin community members

Variant Community Feed

Variant community feed

Learn how to use, manage, and configure the Snippet Library in Franklin

Franklin Snippet Library

Dynamic Snippets

Support

Snippet Library

Find answers and get help from Intercom Support and Community Experts

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