Overview
Syllabus
Introduction
The power of technology
Patient perspective
Big data
Challenges
Opportunities
Regulatory uncertainty
We have to be patient
The burden of public health
Sequencing as monitoring
Ethical considerations
Dont do something just because we can
The DTC genetic community
Genomics as a research tool
Reducing disparities
Access
Disparities
The Great Human Diaspora
Public sophistication
Science literacy
Medical students and the public
Ethics in genomics
Making genetic information more accessible
No comprehensive privacy laws
Evolution of better social models
Jim Evans
Taught by
TEDMED