Ainscough, B. J., Barnell, E. K., Ronning, P., Campbell, K. M., Wagner, A. H., Fehniger, T. A., . . . Griffith, O. L. (2018). A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data. Nature genetics, 50(12), 1735-1743. https://doi.org/10.1038/s41588-018-0257-y
Chicago Style (17th ed.) CitationAinscough, Benjamin J., et al. "A Deep Learning Approach to Automate Refinement of Somatic Variant Calling from Cancer Sequencing Data." Nature Genetics 50, no. 12 (2018): 1735-1743. https://doi.org/10.1038/s41588-018-0257-y.
MLA (9th ed.) CitationAinscough, Benjamin J., et al. "A Deep Learning Approach to Automate Refinement of Somatic Variant Calling from Cancer Sequencing Data." Nature Genetics, vol. 50, no. 12, 2018, pp. 1735-1743, https://doi.org/10.1038/s41588-018-0257-y.