| Literature DB >> 25339190 |
Galen E B Wright1, Adebowale A Adeyemo2, Nicki Tiffin3.
Abstract
Rapid advances in human genomic research are increasing the availability of genomic data for secondary analysis. Particularly in the case of vulnerable African populations, ethics and informed consent processes need to be transparent--both to ensure participant protection, as well as to share skills and to evolve best practice for informed consent from a shared knowledge base. An open dialogue between all stakeholders can facilitate this.Entities:
Mesh:
Year: 2014 PMID: 25339190 PMCID: PMC4445680 DOI: 10.1186/s40246-014-0018-7
Source DB: PubMed Journal: Hum Genomics ISSN: 1473-9542 Impact factor: 4.639