Newborn testing and screening by whole-genome sequencing

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Abstract

Over the course of the next few decades, the availability of cheap, efficient DNA sequencing technology will lead to a medical landscape in which each baby's genome is sequenced, and that information is used to shape a lifetime of personalized strategies for disease prevention, detection, and treatment.

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Kingsmore, S. F. (2016, March 1). Newborn testing and screening by whole-genome sequencing. Genetics in Medicine. Nature Publishing Group. https://doi.org/10.1038/gim.2015.172

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