Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research

Flavia M Facio1, Julie C Sapp, Amy Linn

  • 1National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

BMC Medical Genomics
|October 11, 2012
PubMed
Summary

Informed consent for massively-parallel sequencing (MPS) studies can be clarified by distinguishing between hypothesis-testing and hypothesis-generating approaches. This distinction aids communication and addresses challenges with secondary findings in genetic research.

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