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Approaches to Carrier Testing and Results Disclosure in Translational Genomics Research

dc.contributor.authorClayton, Ellen Wright
dc.contributor.authorPorter, Kathryn M.
dc.contributor.authoret al.
dc.date.accessioned2018-11-05T22:45:50Z
dc.date.available2018-11-05T22:45:50Z
dc.date.issued2017
dc.identifier.citationMolecular Genetics & Genomic Medicine 1-12 (2018)en_US
dc.identifier.urihttp://hdl.handle.net/1803/9327
dc.descriptionarticle published in a medical research journalen_US
dc.description.abstractBackground: Clinical genome and exome sequencing (CGES) is primarily used to address specific clinical concerns by detecting risk of future disease, clarifying diagnosis, or directing treatment. Additionally, CGES makes possible the disclosure of autosomal recessive and X-linked carrier results as additional secondary findings, and research about the impact of carrier results disclosure in this context is needed. Methods: Representatives from 11 projects in the clinical sequencing exploratory research (CSER) consortium collected data from their projects using a structured survey. The survey focused on project characteristics, which variants were offered and/or disclosed to participants as carrier results, methods for carrier results disclosure, and project-specific outcomes. We recorded quantitative responses and report descriptive statistics with the aim of describing the variability in approaches to disclosing carrier results in translational genomics research projects. Results: The proportion of participants with carrier results was related to the number of genes included, ranging from 3% (three genes) to 92% (4,600 genes). Between one and seven results were disclosed to those participants who received any positive result. Most projects offered participants choices about whether to receive some or all of the carrier results. There were a range of approaches to communicate results, and many projects used separate approaches for disclosing positive and negative results. Conclusion: Future translational genomics research projects will need to make decisions regarding whether and how to disclose carrier results. The CSER consortium experience identifies approaches that balance potential participant interest while limiting impact on project resources.en_US
dc.format.extent1 PDF (12 pages)en_US
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherMolecular Genetics & Genomic Medicineen_US
dc.subjectcarrier testingen_US
dc.subjectexomeen_US
dc.subjectgenomeen_US
dc.subjectsecondary findingsen_US
dc.subjecttranslational genomics researchen_US
dc.subject.lcshlawen_US
dc.titleApproaches to Carrier Testing and Results Disclosure in Translational Genomics Researchen_US
dc.title.alternativeThe Clinical Sequencing Exploratory Research Consortium Experienceen_US
dc.typeArticleen_US


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