6 hours
Whitehead Institute
Free Tickets Available
Wed, 12 Nov, 2025 at 09:00 am to 03:00 pm (GMT-05:00)
Whitehead Institute
455 Main Street, Cambridge, United States
Many rare disease patients today still face long "diagnostic odysseys" and low diagnosis yields. The accurate clinical interpretation of rare and novel variants remains a major barrier to diagnosis and treatment.
Currently, clinicians and researchers approach variant analysis very differently. Most clinical genetics insights originate from basic research, yet functional genomics researchers often lack the clinical context necessary to design models that accurately reflect real patient phenotypes. Conversely, clinicians either have limited awareness of genetics or struggle to find researchers with relevant expertise for their patients’ conditions. BridgeRD aims to address this disconnect by:
We invite clinicians, clinical variant scientists, basic science researchers, and AI scientists to accelerate efforts to functionally characterize rare variants, improve clinical care, and drive the field forward.
Practicing clinicians, trainees, and academic and industry professionals are welcome to share their insights and explore potential cross-disciplinary initiatives for accelerating the diagnosis and treatment of rare diseases.
BridgeRD2025 is excited to host a variety of opportunities to learn, collaborate, and brainstorm solutions to challenges in studying and treating rare disease:
Agenda Details:
9:00a - 9:15a: Opening Remarks
9:15a - 9:45a: Keynote
9:45a - 10:45a: Speaker Session I
10:45a - 11:15a: Coffee Break
11:15a - 12:15p: Speaker Session II
12:15p - 12:30p: Closing Remarks
12:30p - 1:30p: Networking Lunch
1:30p - 3:00p: Interactive Problem-Solving Workshop
Also check out other Workshops in Cambridge.
Tickets for BridgeRD: Clinical Genetics Meets Functional Genomics for Rare Diseases can be booked here.
Ticket type | Ticket price |
---|---|
General Admission: In-person | Free |
General Admission: Virtual | Free |