The Need to Standardize the Reanalysis of Genomic Sequencing Results: Findings from Interviews with Underserved Families in Genomic Research
Author:
Publisher
Springer Science and Business Media LLC
Subject
Health Policy,Health (social science)
Link
https://link.springer.com/content/pdf/10.1007/s11673-023-10267-2.pdf
Reference39 articles.
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2. Al-Nabhani, M. S., Al-Rashdi, F., Al-Murshedi, F., et al. 2018. Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits. Clinical Genetics 94(6): 495– 501.
3. Appelbaum, P.S., E. Parens, S.M. Berger, W.K. Chung, and W. Burke. 2020. Is there a duty to reinterpret genetic data? The ethical dimensions. Genetics in Medicine 22(3): 633–639.
4. Aronson, S.J., E.H. Clark, M. Varugheese, S. Baxter, L.J. Babb, and H.L. Rehm. 2012. Communicating new knowledge on previously reported genetic variants. Genetics in Medicine 14(8): 713–719.
5. Baker, S.W., J.R. Murrell, A.I. Nesbitt, et al. 2019. Automated clinical exome reanalysis reveals novel diagnoses. The Journal of Molecular Diagnostics 21(1): 38–48.
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