ASHG 2022 - SOPHiA GENETICS Lunch & Learn

Friday, October 28, 3:30pm - 4:30pm (EDT)

Time shown in-04:00 America, New York

Join us for our Lunch & Learn symposium!

Learn about SOPHiA DDMTM Platform - Enjoy lunch together - Network with your peers

Fully integrated workflows to accurately interpret genomic variants associated with rare and inherited diseases

There are multiple steps involved in gaining insights from next-generation sequencing (NGS) data, which can take considerable time and involve several technologies and providers. In our lunch symposium, hear first-hand about how we collaborate with renowned genomic experts to design and implement cost-effective, tailored NGS-based applications to maximize workflow efficiency.

Discover how our sample-to-report workflows streamline the accurate identification and interpretation of nuclear and mitochondrial variants associated with rare and inherited diseases, including hereditary cancers.

Our speakers will share how the SOPHiA DDMTM Platform adapts to their laboratory’s needs to accurately call and prioritize variants in combination with AlamutTM Visual Plus for deep exploration and full-genome visualization to enhance variant interpretation

Add to Calendar 2022/10/28 12:30:00 2022/10/28 13:30:00 America/Los_Angeles ASHG 2022 - SOPHiA GENETICS Lunch & Learn Join us for our Lunch & Learn symposium!

Learn about SOPHiA DDMTM Platform - Enjoy lunch together - Network with your peers

Fully integrated workflows to accurately interpret genomic variants associated with rare and inherited diseases

There are multiple steps involved in gaining insights from next-generation sequencing (NGS) data, which can take considerable time and involve several technologies and providers. In our lunch symposium, hear first-hand about how we collaborate with renowned genomic experts to design and implement cost-effective, tailored NGS-based applications to maximize workflow efficiency.

Discover how our sample-to-report workflows streamline the accurate identification and interpretation of nuclear and mitochondrial variants associated with rare and inherited diseases, including hereditary cancers.

Our speakers will share how the SOPHiA DDMTM Platform adapts to their laboratory’s needs to accurately call and prioritize variants in combination with AlamutTM Visual Plus for deep exploration and full-genome visualization to enhance variant interpretation 1201 S Figueroa St, Los Angeles, 90015, CA, USA false MM/DD/YYYY 30 OPAQUE axnljDEozzdWjvMNzmGn156867

1201 S Figueroa St, Los Angeles, 90015, CA, USA

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