From Complexity to Clarity: Streamlining Variant Investigation with Alamut™ Visual Plus

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Home breadcrumb-arrow From Complexity to Clarity: Streamlining Variant Investigation with Alamut™ Visual Plus

Join us for an in-depth session on Alamut™ Visual Plus, an advanced variant interpretation software trusted by genetic research laboratories worldwide. This webinar will provide a comprehensive overview of the software’s capabilities—spanning intuitive visualization, integrated genomic annotations, splicing predictions, and ACMG classification support—designed to streamline and standardize variant review and interpretation.

Through a live demonstration, we’ll walk through key features and workflows that enable users to efficiently navigate NGS data, explore variant impacts in genomic context, and make evidence-based classification decisions. Whether you’re a new user seeking to understand the platform or an experienced user looking to optimize your analysis process, this session will showcase how Alamut™ Visual Plus empowers accurate and confident variant interpretation.

Speaker

Yi Lian - Product Director, Platform at SOPHiA GENETICS

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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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