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"Ten years after the sequencing of the human genome, scientists have developed genetic tests that can predict a person's response to certain drugs, estimate the risk of developing Alzheimer's disease, and make other predictions based on known links between genes and diseases. However, genetic tests have yet to become a routine part of medical care, in part because there is not enough evidence to show they help improve patients' health.The Institute of Medicine (IOM) held a workshop to explore how researchers can gather better evidence more efficiently on the clinical utility of genetic tests. Generating Evidence for Genomic Diagnostic Test Development compares the evidence that is required for decisions regarding clearance, use, and reimbursement, to the evidence that is currently generated. The report also addresses innovative and efficient ways to generate high-quality evidence, as well as barriers to generating this evidence. Generating Evidence for Genomic Diagnostic Test Development contains information that will be of great value to regulators and policymakers, payers, health-care providers, researchers, funders, and evidence-based review groups."--Publisher's description.
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Previews available in: English
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1
Generating Evidence for Genomic Diagnostic Test Development: Workshop Summary
2011, National Academies Press
in English
0309211085 9780309211086
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Generating evidence for genomic diagnostic test development: workshop summary
2011, National Academies Press
in English
0309211042 9780309211048
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Generating Evidence for Genomic Diagnostic Test Development: Workshop Summary
2011, National Academies Press
in English
0309211050 9780309211055
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Generating Evidence for Genomic Diagnostic Test Development: Workshop Summary
2011, National Academies Press
in English
0309211077 9780309211079
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Book Details
Edition Notes
Includes bibliographical references (p. 63-66).
Also available in Open Book format via the National Academies Press home page.
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