Holly Etchegary

Memorial University of Newfoundland, Faculty of Medicine

Faculty of Medicine

St. John's, Newfoundland A1B 3X5 A1C 5V3








Scholarly Papers (1)


Reflections on the Cost of 'Low Cost' Whole Genome Sequencing: Framing the Health Policy Debate

PLOS Biology, V. 11, No. 11, November 2013, p. e1001699, U of Maryland Legal Studies Research Paper No. 2013-68
Number of pages: 6 Posted: 12 Nov 2013
University of Alberta - Health Law Institute, University of North Carolina (UNC) at Chapel Hill - School of Medicine, Baylor College of Medicine, University of Alberta - Emergency Medicine, University of Alberta - Faculty of Public Health, Arizona State University (ASU) - School for the Future of Innovation in Society, McGill University - BioMedical Ethics Unit, King’s College London, Dept of Social Science, Health & Medicine, University of Toronto - Institute of Health Policy, Management and Evaluation, University of Montreal, Dept of Social and Preventive Medicine, National Institutes of Health (NIH) - National Human Genome Research Institute, Catholic University of Leuven - Faculty of Medicine - Center for Biomedical Ethics and Law, Stanford University - Stanford Center for Biomedical Ethics (SCBE), University of Toronto, Granovsky Gluskin Family Medicine Centre, Memorial University of Newfoundland, Faculty of Medicine, McGill University - Centre for Genomics and Policy, Osaka, Dept of Biomedical Ethics & Public Policy, Graduate School of Medicine, Stanford University - Stanford Center for Biomedical Ethics (SCBE), University of Maryland Francis King Carey School of Law, University of Pennsylvania - Perelman School of Medicine, University of Toronto, Centre for Bioethics, University of Wisconsin-Madison, School of Law; Morgridge Institute for Research, Memorial University of Newfoundland - Faculty of Medicine, Université Laval - Faculty of Medicine, University of Toronto - Department of Health Policy, Management and Evaluation and University of Ottawa, Faculty of Medicine, Public Health Genomics
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whole genome sequencing, WGS, whole exome sequencing, WES, human genome