Details

Join us for an interactive, team-based workshop designed to accelerate genomic interpretation skills and collaboration. This session blends the energy of a hackathon with a structured learning environment to revisit real-world, unresolved pediatric cases.
 

What You’ll Experience:

  • Collaborative, case-based problem solving in a guided workshop format 
  • Hands-on analysis using advanced genomic technologies
  • Team presentations and shared insights across groups

What You’ll Learn:

  • Key interpretation techniques, including:
    Variant filtering
    Annotation
    Phenotype–genotype correlation 
  • Strategies to improve efficiency and reduce time to diagnosis

Who Should Attend:

  • Physicians 
  • Clinical geneticists and researchers 
  • Bioinformaticians and variant analysts 
  • Cross-functional clinical and research teams

Event Details

  • Time: October 8 from 9 AM to 5 PM ET
  • Location: Boston Children Hospital - 300 Longwood Ave, Boston, MA 02115
  • Cost: Free (registration required)
  • Capacity: Limited to maintain an interactive experience; register early
  • Includes: Lunch and refreshments
Register now
Date & Time
8 Oct. 2026
09:00 AM - 05:00 PM
Location
Boston Children Hospital
Capacity
Register now as capacity is limited to maintain an interactive experience.
Topic
Genetic & rare diseases
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