APA (7th ed.) Citation

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.) Citation

Ainscough, 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.) Citation

Ainscough, 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.

Warning: These citations may not always be 100% accurate.