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  1. franklin.genoox.com › homeFranklin - Genoox

    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.

  2. franklin2.genoox.com › clinical-db › homeFranklin

    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

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

    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.

  4. help.genoox.com › en › articlesFranklin suggested classification | Franklin Help Center - Genoox

    Franklin employs an advanced classification tool based on ACMG guidelines, to automatically identify and prioritize pathogenic variants. The classification tool is powered by artificial intelligence technology and supports inside organization workflows of classification using a hierarchy scheme automatically ranking variants by using user ...

  5. help.genoox.com › en › articlesFranklin's AI-based variant prioritization engine

    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.

  6. franklinbygenoox.medium.com › new-oncogenicityNew oncogenicity classification guidelines for somatic variants

    Mar 29, 2022 · This work defines variant oncogenicity as the pathogenicity of the variant in the context of neoplastic disease and relies on different lines of evidence, such as population frequency,...

  7. pubmed.ncbi.nlm.nih.gov › 35101336Standards for the classification of pathogenicity of somatic ...

    Results: This comprehensive SOP has been developed to improve consistency in somatic variant classification and has been validated on 94 somatic variants in 10 common cancer-related genes. Conclusion: The comprehensive SOP is now available for classification of oncogenicity of somatic variants.