A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health

Abstract excerpt

points• There is currently insufficient scientific evidence to support routine nondiagnostic use of germline genome sequencing in healthcare settings and population screening, but an increasing number of health systems are piloting genomic sequencing projects for clinical care.• In principle, numerous diagnostic or prognostic tests based on genes or variants could be used for different purposes across the life...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Cancer Genomics and Diagnostics
• Share to Ethics in Clinical Research
• Share to Genomics and Rare Diseases