APA (7th ed.) Citation

Wünsch, C., Banck, H., Müller-Tidow, C., & Dugas, M. (2020). AMLVaran: A software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting. BMC Medical Genomics, 13(1), 1. https://doi.org/10.1186/s12920-020-0668-3

Chicago Style (17th ed.) Citation

Wünsch, Christian, Henrik Banck, Carsten Müller-Tidow, and Martin Dugas. "AMLVaran: A Software Approach to Implement Variant Analysis of Targeted NGS Sequencing Data in an Oncological Care Setting." BMC Medical Genomics 13, no. 1 (2020): 1. https://doi.org/10.1186/s12920-020-0668-3.

MLA (9th ed.) Citation

Wünsch, Christian, et al. "AMLVaran: A Software Approach to Implement Variant Analysis of Targeted NGS Sequencing Data in an Oncological Care Setting." BMC Medical Genomics, vol. 13, no. 1, 2020, p. 1, https://doi.org/10.1186/s12920-020-0668-3.