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Clinical Integration of Next Generation Sequencing: A Policy Analysis

Overview of attention for article published in The Journal of Law, Medicine & Ethics, January 2021
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Title
Clinical Integration of Next Generation Sequencing: A Policy Analysis
Published in
The Journal of Law, Medicine & Ethics, January 2021
DOI 10.1111/jlme.12158
Pubmed ID
Authors

David Kaufman, Margaret Curnutte, Amy L. McGuire

Abstract

Clinical next generation sequencing (NGS) technologies are challenging existing regulatory paradigms. We advocate a coordinate policy approach, which first requires a comprehensive understanding of the existing regulatory and legal structures. This paper introduces four key policy domains - including quality assurance, insurance coverage, intellectual property management, and data sharing - that must be addressed to ensure high quality clinical NGS. In bringing these policy issues into conversation through this special issue for the Journal of Law, Medicine & Ethics, we hope to lay the foundation for further discussion by a range of stakeholder groups with diverse and strong interests in the governance of NGS.

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Mendeley readers

The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 7%
Argentina 1 3%
Unknown 26 90%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 28%
Student > Master 5 17%
Other 4 14%
Student > Ph. D. Student 4 14%
Student > Bachelor 4 14%
Other 2 7%
Unknown 2 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 11 38%
Social Sciences 6 21%
Biochemistry, Genetics and Molecular Biology 3 10%
Medicine and Dentistry 3 10%
Economics, Econometrics and Finance 1 3%
Other 2 7%
Unknown 3 10%