1932

Abstract

An ethical quandary is emerging over custodianship of and access to DNA specimens and attached data, clinical and genetic, held in large disease cohort collections. The balance of patients’ rights and science/society's quest for broad open access must be resolved in order to realize the promise of gene association studies of complex human disease. A way forward may be to convene a colloquium of international medical and science organizations charged with developing global consensus guidance and ethical principles for access to and use of genomic biobanks.

Loading

Article metrics loading...

/content/journals/10.1146/annurev-genom-082908-150133
2009-09-22
2024-12-11
Loading full text...

Full text loading...

/content/journals/10.1146/annurev-genom-082908-150133
Loading
/content/journals/10.1146/annurev-genom-082908-150133
Loading

Data & Media loading...

  • Article Type: Review Article
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error