What’s new in Alamut™ Visual Plus 2.2: Sanger Deconvolution and Real-World Variant Interpretation

Date: December 2, 2026 - December 2, 2026
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Home breadcrumb-arrow What’s new in Alamut™ Visual Plus 2.2: Sanger Deconvolution and Real-World Variant Interpretation

Alamut™ Visual Plus 2.2 is releasing soon, and we’re hosting a live webinar to mark the occasion. Join us to see what’s new in the release and how your peers in the field use Alamut™ Visual Plus in their daily variant interpretation work.

What you’ll see:

  • Real lab workflows: Experienced Alamut™ Visual Plus users walk through their own variant interpretation process, from nomenclature review to ACMG classification, and share what they rely on day to day.
  • A first look at 2.2: Dermot Adelmann of SOPHiA GENETICS demos the new release live, including:
    • Sanger deconvolution: powered by the Tracy tool, detect heterozygous variants and export results directly from the Sanger track
    • Occurence management
    • Clearer ACMG classification
    • Workflow improvements

Whether you’ve used Alamut™ Visual Plus for years or are evaluating interpretation tools, you’ll leave with practical ideas to bring back to your own lab.

Register Now

Disclaimer notice:
The term SOPHIA used by the speaker refers to SOPHiA GENETICS and its products.
The opinions expressed during this presentation are those of the speakers and may not represent the opinions of SOPHiA GENETICS.
SOPHiA GENETICS does not provide support in the validation of custom products for clinical use.
SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us at [email protected] to obtain the appropriate product information for your country of residence.

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise.

SOPHiA DDM™ Dx Hereditary Cancer Solution, SOPHiA DDM™ Dx RNAtarget Oncology Solution and SOPHiA DDM™ Dx Homologous Recombination Deficiency Solution are available as CE-IVD products for In Vitro Diagnostic Use in the European Economic Area (EEA), the United Kingdom and Switzerland. SOPHiA DDM™ Dx Myeloid Solution and SOPHiA DDM™ Dx Solid Tumor Solution are available as CE-IVD products for In Vitro Diagnostic Use in the EEA, the United Kingdom, Switzerland, and Israel. Information about products that may or may not be available in different countries and if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact us to obtain the appropriate product information for your country of residence.

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