Cite
Resolving the full spectrum of human genome variation using Linked-Reads.
MLA
Marks, Patrick, et al. “Resolving the Full Spectrum of Human Genome Variation Using Linked-Reads.” Genome Research, vol. 29, no. 4, Apr. 2019, pp. 635–45. EBSCOhost, https://doi.org/10.1101/gr.234443.118.
APA
Marks, P., Garcia, S., Barrio, A. M., Belhocine, K., Bernate, J., Bharadwaj, R., Bjornson, K., Catalanotti, C., Delaney, J., Fehr, A., Fiddes, I. T., Galvin, B., Heaton, H., Herschleb, J., Hindson, C., Holt, E., Jabara, C. B., Jett, S., Keivanfar, N., … Church, D. M. (2019). Resolving the full spectrum of human genome variation using Linked-Reads. Genome Research, 29(4), 635–645. https://doi.org/10.1101/gr.234443.118
Chicago
Marks, Patrick, Sarah Garcia, Alvaro Martinez Barrio, Kamila Belhocine, Jorge Bernate, Rajiv Bharadwaj, Keith Bjornson, et al. 2019. “Resolving the Full Spectrum of Human Genome Variation Using Linked-Reads.” Genome Research 29 (4): 635–45. doi:10.1101/gr.234443.118.