APA (7th ed.) Citation

Q, D., C, S., R, M., B, T., MS, R., K, K., . . . RK, J. (2023). SCIP: Software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing. Human genetics, 142(2), 201. https://doi.org/10.1007/s00439-022-02494-1

Chicago Style (17th ed.) Citation

Q, Ding, et al. "SCIP: Software for Efficient Clinical Interpretation of Copy Number Variants Detected by Whole-genome Sequencing." Human Genetics 142, no. 2 (2023): 201. https://doi.org/10.1007/s00439-022-02494-1.

MLA (9th ed.) Citation

Q, Ding, et al. "SCIP: Software for Efficient Clinical Interpretation of Copy Number Variants Detected by Whole-genome Sequencing." Human Genetics, vol. 142, no. 2, 2023, p. 201, https://doi.org/10.1007/s00439-022-02494-1.