Helix Events
2026 ACMG Annual Clinical Genetics Meeting
Join us live at the American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting in Baltimore, MD from March 10-14, 2026 and learn about Helix's latest innovations in research.
Meet our experts at Booth #817!
Clinical genomics
Same test today. Infinite possibilities tomorrow. The only platform built for lifelong clinical utility.
Sequence Once, Query Often®
Exome+® backbone, lifelong access
One sample becomes a lifetime of queryable data—enabling rapid clinical updates without the need for repeat chemistry.
Helix Wayfinder™
AI-powered insights at scale
Specialized AI agents interrogate every variant in Helix’s assay against global evidence, and synthesize ndings against ACMG/AMP standards.
Genetic Risk Assessment
Automated screening, clinical focus
Automate family history and consenting to quickly flag patients appropriate for testing, shifting your focus from administration to high-value clinical management.
Poster & Platform Talks
Helix Research Network scientists will be presenting several posters and talks on genomics, data and patient care.
Platform Talk
Title: Rare pathogenic, polygenic, and structural variant analysis in sarcomere-negative HCM patients of African and European genetic ancestry from 15 health systems
Presented by: Kelly Schiabor Barrett, PhD
Date: Wednesday, March 11th 2026
Time and Location: 12:30 pm – 12:45 pm, Room 318-323
Platform Talk
Title: From Uncertain to Actionable: Significant Reduction in Variants of Uncertain Significance in Hereditary Germline Testing via Multi-Institutional Real-World Evidence
Presented by: Liz Cirulli, PhD
Date: Wednesday, March 11th 2026
Time and Location: 1:00 pm – 1:15 pm, Room 318-323
Poster Presentations
Title: P141 Genetic Identification of Fabry Disease Reveals a High Burden of Undiagnosed Phenotypes and Reduces Diagnostic Workup
Presented by: Liz Cirulli, PhD., Associate Director, Research
Date: Thursday, March 12th, 2026
Time: 10:30am – 11:30am ET
Title: P234 Predicting Chronic Kidney Disease Following Mild Kidney Dysfunction: An Integrated Multi-Trait Polygenic and Clinical Risk Model with Multi-Site External Validation
Presented by: Liz Cirulli, PhD., Associate Director, Research
Date: Friday, March 13th, 2026
Time: 10:30am – 11:30am ET
Title: P510 Genetic Counseling Uptake and Reasons for Decline After Receipt of Positive CDCT1 Test Results in a Population Health Setting
Presented by: Kate Lynch, Associate Director, Medical Information & Communications
Date: Friday, March 13th, 2026
Time: 10:30am – 11:30am ET