A, T., J, L., J, N., C, H., J, T., K, C., . . . D, P. (2014). SMaSH: A benchmarking toolkit for human genome variant calling. Bioinformatics (Oxford, England), 30(19), 2787. https://doi.org/10.1093/bioinformatics/btu345
Chicago Style (17th ed.) CitationA, Talwalkar, et al. "SMaSH: A Benchmarking Toolkit for Human Genome Variant Calling." Bioinformatics (Oxford, England) 30, no. 19 (2014): 2787. https://doi.org/10.1093/bioinformatics/btu345.
MLA (9th ed.) CitationA, Talwalkar, et al. "SMaSH: A Benchmarking Toolkit for Human Genome Variant Calling." Bioinformatics (Oxford, England), vol. 30, no. 19, 2014, p. 2787, https://doi.org/10.1093/bioinformatics/btu345.
Warning: These citations may not always be 100% accurate.