APA (7th ed.) Citation

S, S., HP, H., A, V., Z, F., A, E., TP, K., . . . B, T. (2025). Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis. Frontiers in genetics, 16, 1499456. https://doi.org/10.3389/fgene.2025.1499456

Chicago Style (17th ed.) Citation

S, Sen, et al. "Validation of a Comprehensive Long-read Sequencing Platform for Broad Clinical Genetic Diagnosis." Frontiers in Genetics 16 (2025): 1499456. https://doi.org/10.3389/fgene.2025.1499456.

MLA (9th ed.) Citation

S, Sen, et al. "Validation of a Comprehensive Long-read Sequencing Platform for Broad Clinical Genetic Diagnosis." Frontiers in Genetics, vol. 16, 2025, p. 1499456, https://doi.org/10.3389/fgene.2025.1499456.