This Genomics and Precision Health essay discusses the risks and potential benefits of performing genome sequencing in healthy people.
This Viewpoint discusses sharing the underlying data of genetic testing to develop more precise disease risk estimates and understand whether physicians should act on them.
This Editorial discusses possible contributions of genomic sequencing to progress in clinical care, from molecular diagnosis to improved outcomes.
Dewey and colleagues found that depending on the sequencing platform used, there was incomplete coverage of inherited disease genes, low reproducibility of potentially clinically significant genetic variation, and uncertainty about clinically reportable findings.
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