Toward clinical genomics in everyday medicine: perspectives and recommendations

Susan Delaney(Coriell Institute For Medical Research), Michael Hultner(Lockheed Martin (United States)), Howard J. Jacob(HudsonAlpha Institute for Biotechnology), David H. Ledbetter(Geisinger Health System), Jeanette McCarthy(Duke University), M.A. Ball, Kenneth B. Beckman(University of Minnesota), John W. Belmont(Children's Nutrition Research Center at Baylor College of Medicine), Cinnamon S. Bloss(University of California San Diego), Michael F. Christman(Coriell Institute For Medical Research), Andy Cosgrove, Stephen A. Damiani(Mission Australia), Timothy Danis, Massimo Delledonne(University of Verona), Michael J. Dougherty(American Society of Human Genetics), Joel T. Dudley(Icahn School of Medicine at Mount Sinai), W. Andrew Faucett(Geisinger Health System), Jennifer Friedman(University of California San Diego), David H. Haase(Maxwell Technologies (United States)), T S Hays(University of Minnesota), Stu Heilsberg, Jeff Huber(Google (United States)), Leah Kaminsky, Nikki Ledbetter(Geisinger Health System), Warren H. Lee, Elissa Levin(Icahn School of Medicine at Mount Sinai), Ondrej Libiger(Revolution Analytics (United States)), Michael D. Linderman(Icahn School of Medicine at Mount Sinai), Richard L. Love, David Magnus(Stanford Medicine), AnneMarie Martland(Revolution Analytics (United States)), Susan L. McClure(ScienceMedia (United States)), Scott E. Megill(Coriell Institute For Medical Research), Helen Messier, Robert L. Nussbaum(Invitae (United States)), Latha Palaniappan(Palo Alto University), Bradley Patay(Scripps Clinic Medical Group), Bradley W. Popovich(Genome British Columbia), John Quackenbush(Dana-Farber Cancer Institute), Mark J. Savant(California Wellness Foundation), Michael M. Su(Anthem (United States)), Sharon F. Terry(Genetic Alliance), Steven Tucker(Mount Elizabeth Novena Hospital), William T. Wong(Creative Commons), Robert C. Green(Broad Institute)
Expert Review of Molecular Diagnostics
January 26, 2016
Cited by 105Open Access
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Abstract

Precision or personalized medicine through clinical genome and exome sequencing has been described by some as a revolution that could transform healthcare delivery, yet it is currently used in only a small fraction of patients, principally for the diagnosis of suspected Mendelian conditions and for targeting cancer treatments. Given the burden of illness in our society, it is of interest to ask how clinical genome and exome sequencing can be constructively integrated more broadly into the routine practice of medicine for the betterment of public health. In November 2014, 46 experts from academia, industry, policy and patient advocacy gathered in a conference sponsored by Illumina, Inc. to discuss this question, share viewpoints and propose recommendations. This perspective summarizes that work and identifies some of the obstacles and opportunities that must be considered in translating advances in genomics more widely into the practice of medicine.


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