Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues
Share this article
Click the icon of the social media platform on which you would like to share this article.
Email this article to a friend
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Other content recommended for you
- Guideline for feedback of individual genetic research findings for genomics research in Africa
- Taking it to the bank: the ethical management of individual findings arising in secondary research
- Should institutions fund the feedback of individual findings in genomic research?
- Cardiovascular genetics: the role of genetic testing in diagnosis and management of patients with hypertrophic cardiomyopathy
- Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management
- Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases
- Whole-genome sequencing
- The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists
- Modern genomic techniques in the identification of genetic causes of cardiomyopathy
- Rare MYC-N11S germline mutation indicative of inherited breast cancer in a multigeneration family