Alamut Visual Plus v2.1: See What's New, Unlock What's Possible

Date: June 17, 2026June 17, 2026
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Home breadcrumb-arrow Alamut Visual Plus v2.1: See What's New, Unlock What's Possible

17th June 2026 | Time 4PM CET / 10 AM EST

Are you getting everything Alamut Visual Plus has to offer? Join us on June 17th for a live webinar that takes a comprehensive look at Alamut Visual Plus, the variant interpretation platform built around ACMG/AMP guidelines and trusted by clinical and research genomics teams worldwide. Whether you are already using AVP day-to-day or exploring it for the first time, this session is designed to show you what best-in-class variant interpretation looks like in practice.

We will walk through the full capabilities of the platform and introduce the most exciting additions in the v2.1 release, including enhanced Sanger visualization that brings confirmatory sequencing data seamlessly into your interpretation workflow, and newly integrated ClinGen framework support for evidence-based oncogenicity classification alongside established germline guidelines.

This is a session built for scientists and clinicians who want to interpret variants faster, more consistently, and with greater confidence.

Register now to secure your spot.

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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.

All third-party trademarks listed by SOPHiA GENETICS remain the property of their respective owners. Unless specifically identified as such, SOPHiA GENETICS’ use of third-party trademarks does not indicate any relationship, sponsorship, or endorsement between SOPHiA GENETICS and the owners of these trademarks. Any references by SOPHiA GENETICS to third-party trademarks is to identify the corresponding third-party goods and/or services and shall be considered nominative fair use under the trademark law.

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