Conferences & Events
Join us at upcoming conferences to connect and discuss the future of exome and genome sequencing.
Upcoming Conferences
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Connect with GeneDx at CHNC 2026 to learn how rapid genome sequencing can help NICU teams uncover the genetic causes of complex conditions, inform care decisions, and provide answers for infants and their families.
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Connect with GeneDx at ASHG 2026 to discover how the largest rare disease dataset is powering more precise genetic answers.
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Connect with GeneDx at SDBP 2026.
Join GeneDx at Becker’s to discuss how genetic testing can support your organization’s goals and the patients you serve. Schedule a meeting with our team to explore opportunities to work together.
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Connect with GeneDx at NSGC to explore genetic testing, discover resources for genetic counselors, and learn how we can help you find answers for your patients.
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Connect with GeneDx at AES 2026 to learn how exome and genome sequencing can help uncover the genetic causes of epilepsy, inform clinical management, and provide answers for patients and families.
Booth #1805
Past Conferences
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Connect with GeneDx at CNS 2026 to learn how exome and genome sequencing can help uncover the genetic causes of complex neurological conditions, inform clinical management, and provide answers for children and their families.
Booth #601
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Connect with GeneDx at the 2026 Rare Trials Summit, September 14–16 in Boston, to explore how genomic insights can help accelerate rare disease drug development.
On Tuesday, September 15 from 9:00–9:30 a.m., join Colleen Caleshu, MSc, LCGC, Senior Director of Translational Research at GeneDx, for “From Data to Discovery: Finding the Right Patients for Rare Disease Trials.” The session will explore how combining genetically confirmed cohorts with rich phenotypic and longitudinal real-world data can improve patient identification and clinical trial planning.
Ready to bring genetic testing into your practice?
We’re here to support every step.

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