Cite
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation.
MLA
Lincoln, Stephen E., et al. “One in Seven Pathogenic Variants Can Be Challenging to Detect by NGS: An Analysis of 450,000 Patients with Implications for Clinical Sensitivity and Genetic Test Implementation.” Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 23, no. 9, Sept. 2021, pp. 1673–80. EBSCOhost, https://doi.org/10.1038/s41436-021-01187-w.
APA
Lincoln, S. E., Hambuch, T., Zook, J. M., Bristow, S. L., Hatchell, K., Truty, R., Kennemer, M., Shirts, B. H., Fellowes, A., Chowdhury, S., Klee, E. W., Mahamdallie, S., Cleveland, M. H., Vallone, P. M., Ding, Y., Seal, S., DeSilva, W., Tomson, F. L., Huang, C., … Nussbaum, R. L. (2021). One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation. Genetics in Medicine : Official Journal of the American College of Medical Genetics, 23(9), 1673–1680. https://doi.org/10.1038/s41436-021-01187-w
Chicago
Lincoln, Stephen E, Tina Hambuch, Justin M Zook, Sara L Bristow, Kathryn Hatchell, Rebecca Truty, Michael Kennemer, et al. 2021. “One in Seven Pathogenic Variants Can Be Challenging to Detect by NGS: An Analysis of 450,000 Patients with Implications for Clinical Sensitivity and Genetic Test Implementation.” Genetics in Medicine : Official Journal of the American College of Medical Genetics 23 (9): 1673–80. doi:10.1038/s41436-021-01187-w.