You’re invited to join Illumina at the upcoming ACMG 2022 event. With the increased demand of WES and WGS and the ever-expansion of gene panels, we are bringing you implementation solutions for WGS-as-a-backbone assay, carving out panels virtually for reporting.
Book with us your demo of Illumina’s XAI (explainable AI) data interpretation solution, Emedgene, which is accelerated by DRAGEN™. You will experience how to power your germline digital workflows starting with your Illumina sequencing instrument, end-to-end.
We’ll have dynamic discussion around pediatric neurology research, the recent NICUSeq study, recent test utilitization studies, and more. After the talks, join us in the booth, get your hands on Emedgene or learn from an interpretation expert, and celebrate the many milestones in the medical genomics field that we are so honored to be part of with you as our partner.
Thursday, March 24, at 10:30 AM CDT
As whole genome sequencing begins to gain acceptance in clinical practice, most regional centers must rely on external reference laboratories to provide sequencing and interpretive services. We describe our institution's experience with implementation of whole genome sequencing with structural variant detection for large, targeted panels and whole exome analyses. By leveraging direct relationships between our laboratory and clinicians, this approach facilitates efficient molecular diagnoses for our patients.
Matthew Bower, MS, LGC
Licensed Genetic Counselor
University of Minnesota Medical Center, Fairview
We are hosting private demos from the Illumina booth. Schedule your session now with a data interpretation expert and sequencing solutions expert for a hands-on, interactive learning experience tailored to your use case. Submit a meeting request