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Genome Sequencing Technologies and Nursing

Author(s)
Taylor, Jacquelyn Y.; Wright, Michelle L.; Hickey, Kathleen T.; Housman, David E
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Abstract
Background Advances in DNA sequencing technology have resulted in an abundance of personalized data with challenging clinical utility and meaning for clinicians. This wealth of data has potential to dramatically impact the quality of healthcare. Nurses are at the focal point in educating patients regarding relevant healthcare needs; therefore, an understanding of sequencing technology and utilizing these data are critical. Aim The objective of this study was to explicate the role of nurses and nurse scientists as integral members of healthcare teams in improving understanding of DNA sequencing data and translational genomics for patients. Approach A history of the nurse role in newborn screening is used as an exemplar. Discussion This study serves as an exemplar on how genome sequencing has been utilized in nursing science and incorporates linkages of other omics approaches used by nurses that are included in this special issue. This special issue showcased nurse scientists conducting multi-omic research from various methods, including targeted candidate genes, pharmacogenomics, proteomics, epigenomics, and the microbiome. From this vantage point, we provide an overview of the roles of nurse scientists in genome sequencing research and provide recommendations for the best utilization of nurses and nurse scientists related to genome sequencing.
Date issued
2017-03
URI
http://hdl.handle.net/1721.1/116521
Department
Massachusetts Institute of Technology. Department of Biology
Journal
Nursing Research
Publisher
Ovid Technologies (Wolters Kluwer Health)
Citation
Taylor, Jacquelyn Y. et al. “Genome Sequencing Technologies and Nursing.” Nursing Research 66, 2 (March 2017): 198–205 © Wolters Kluwer Health, Inc
Version: Author's final manuscript
ISSN
0029-6562

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