Literature DB >> 25298287

Clinical integration of next generation sequencing: a policy analysis.

David Kaufman1, 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.
© 2014 American Society of Law, Medicine & Ethics, Inc.

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Year:  2014        PMID: 25298287      PMCID: PMC5095695          DOI: 10.1111/jlme.12158

Source DB:  PubMed          Journal:  J Law Med Ethics        ISSN: 1073-1105            Impact factor:   1.718


  12 in total

1.  Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.

Authors:  Sarah E Calvo; Alison G Compton; Steven G Hershman; Sze Chern Lim; Daniel S Lieber; Elena J Tucker; Adrienne Laskowski; Caterina Garone; Shangtao Liu; David B Jaffe; John Christodoulou; Janice M Fletcher; Damien L Bruno; Jack Goldblatt; Salvatore Dimauro; David R Thorburn; Vamsi K Mootha
Journal:  Sci Transl Med       Date:  2012-01-25       Impact factor: 17.956

2.  First FDA authorization for next-generation sequencer.

Authors:  Francis S Collins; Margaret A Hamburg
Journal:  N Engl J Med       Date:  2013-11-19       Impact factor: 91.245

3.  Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology.

Authors:  Iris Schrijver; Nazneen Aziz; Daniel H Farkas; Manohar Furtado; Andrea Ferreira Gonzalez; Timothy C Greiner; Wayne W Grody; Tina Hambuch; Lisa Kalman; Jeffrey A Kant; Roger D Klein; Debra G B Leonard; Ira M Lubin; Rong Mao; Narasimhan Nagan; Victoria M Pratt; Mark E Sobel; Karl V Voelkerding; Jane S Gibson
Journal:  J Mol Diagn       Date:  2012-08-20       Impact factor: 5.568

4.  Realizing the opportunities of genomics in health care.

Authors:  Geoffrey S Ginsburg
Journal:  JAMA       Date:  2013-04-10       Impact factor: 56.272

Review 5.  Opening Pandora's Box--the new biology of driver mutations and clonal evolution in cancer as revealed by next generation sequencing.

Authors:  Qianli C Ma; Catherine A Ennis; Samuel Aparicio
Journal:  Curr Opin Genet Dev       Date:  2012-03-01       Impact factor: 5.578

6.  Development of the clinical next-generation sequencing industry in a shifting policy climate.

Authors:  Margaret A Curnutte; Karen L Frumovitz; Juli M Bollinger; Amy L McGuire; David J Kaufman
Journal:  Nat Biotechnol       Date:  2014-10       Impact factor: 54.908

7.  Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.

Authors:  Rossa W K Chiu; Ranjit Akolekar; Yama W L Zheng; Tak Y Leung; Hao Sun; K C Allen Chan; Fiona M F Lun; Attie T J I Go; Elizabeth T Lau; William W K To; Wing C Leung; Rebecca Y K Tang; Sidney K C Au-Yeung; Helena Lam; Yu Y Kung; Xiuqing Zhang; John M G van Vugt; Ryoko Minekawa; Mary H Y Tang; Jun Wang; Cees B M Oudejans; Tze K Lau; Kypros H Nicolaides; Y M Dennis Lo
Journal:  BMJ       Date:  2011-01-11

8.  Assuring the quality of next-generation sequencing in clinical laboratory practice.

Authors:  Amy S Gargis; Lisa Kalman; Meredith W Berry; David P Bick; David P Dimmock; Tina Hambuch; Fei Lu; Elaine Lyon; Karl V Voelkerding; Barbara A Zehnbauer; Richa Agarwala; Sarah F Bennett; Bin Chen; Ephrem L H Chin; John G Compton; Soma Das; Daniel H Farkas; Matthew J Ferber; Birgit H Funke; Manohar R Furtado; Lilia M Ganova-Raeva; Ute Geigenmüller; Sandra J Gunselman; Madhuri R Hegde; Philip L F Johnson; Andrew Kasarskis; Shashikant Kulkarni; Thomas Lenk; C S Jonathan Liu; Megan Manion; Teri A Manolio; Elaine R Mardis; Jason D Merker; Mangalathu S Rajeevan; Martin G Reese; Heidi L Rehm; Birgitte B Simen; Joanne M Yeakley; Justin M Zook; Ira M Lubin
Journal:  Nat Biotechnol       Date:  2012-11       Impact factor: 54.908

Review 9.  Informatics and clinical genome sequencing: opening the black box.

Authors:  Sowmiya Moorthie; Alison Hall; Caroline F Wright
Journal:  Genet Med       Date:  2012-09-13       Impact factor: 8.822

Review 10.  Recommendations for returning genomic incidental findings? We need to talk!

Authors:  Wylie Burke; Armand H Matheny Antommaria; Robin Bennett; Jeffrey Botkin; Ellen Wright Clayton; Gail E Henderson; Ingrid A Holm; Gail P Jarvik; Muin J Khoury; Bartha Maria Knoppers; Nancy A Press; Lainie Friedman Ross; Mark A Rothstein; Howard Saal; Wendy R Uhlmann; Benjamin Wilfond; Susan M Wolf; Ron Zimmern
Journal:  Genet Med       Date:  2013-08-01       Impact factor: 8.822

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  3 in total

1.  FDA's Proposed Guidance for Laboratory Developed Tests: How Should Regulators Balance the Risks and Promise of Innovation in Clinical Genetics?

Authors:  Michelle Bayefsky; Benjamin E Berkman
Journal:  FDLIs Food Drug Policy Forum       Date:  2015-02-25

2.  Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions.

Authors:  Donna A Messner; Pei Koay; Jennifer Al Naber; Robert Cook-Deegan; Mary Majumder; Gail Javitt; Rachel Dvoskin; Juli Bollinger; Margaret Curnutte; Amy L McGuire
Journal:  Per Med       Date:  2017-06-23       Impact factor: 2.512

3.  Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel.

Authors:  Donna A Messner; Jennifer Al Naber; Pei Koay; Robert Cook-Deegan; Mary Majumder; Gail Javitt; Patricia Deverka; Rachel Dvoskin; Juli Bollinger; Margaret Curnutte; Subhashini Chandrasekharan; Amy McGuire
Journal:  Appl Transl Genom       Date:  2016-05-25
  3 in total

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