APA (7th ed.) Citation

De La Vega, F. M., Chowdhury, S., Moore, B., Frise, E., McCarthy, J., Hernandez, E. J., . . . Huentelman, M. (2021). Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases. Genome Medicine, 13(1), 1. https://doi.org/10.1186/s13073-021-00965-0

Chicago Style (17th ed.) Citation

De La Vega, Francisco M., et al. "Artificial Intelligence Enables Comprehensive Genome Interpretation and Nomination of Candidate Diagnoses for Rare Genetic Diseases." Genome Medicine 13, no. 1 (2021): 1. https://doi.org/10.1186/s13073-021-00965-0.

MLA (9th ed.) Citation

De La Vega, Francisco M., et al. "Artificial Intelligence Enables Comprehensive Genome Interpretation and Nomination of Candidate Diagnoses for Rare Genetic Diseases." Genome Medicine, vol. 13, no. 1, 2021, p. 1, https://doi.org/10.1186/s13073-021-00965-0.