Methods: An integrative literature review that examined research studies on both animals and humans that focused on exome and whole genome sequencing use in nursing science via PubMed/ MEDLINE and CINAHL with no date restriction to current.
Results: No studies were found in the nursing literature that focus on the role of the nurse or advanced practice nurses in collecting, reviewing, and disclosing results from whole genome sequencing to patients.
Conclusion: The identification of consequential genetic variants for actionable health conditions is an important area for advancement in nursing research and practice. Nurses are uniquely positioned to provide the effective translation of powerful genomic technologies into positive health care outcomes for the American population, and other populations worldwide. As nurse scientists and genetic counselors consider genome sequencing use in the clinical and community settings, it is important for us to think about the usefulness of this technology as a screening tool and how it has been used in the past to identify heritable disorders in programs such as prenatal screening. Nurses in the United States from either the International Society of Nurses in Genetics nor the American Academy of Nursing Genetic Healthcare Expert Panel have currently published statements or policy briefs on this issue of genome sequencing as a screening tool, however, we are certain that these will be forthcoming.