KucharÃk, M.; BudiÅ¡, J.; Hýblová, M.; Minárik, G.; Szemes, T.
Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH. Diagnostics 2021, 11, 708.
https://doi.org/10.3390/diagnostics11040708
AMA Style
KucharÃk M, BudiÅ¡ J, Hýblová M, Minárik G, Szemes T.
Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH. Diagnostics. 2021; 11(4):708.
https://doi.org/10.3390/diagnostics11040708
Chicago/Turabian Style
KucharÃk, Marcel, Jaroslav BudiÅ¡, Michaela Hýblová, Gabriel Minárik, and Tomáš Szemes.
2021. "Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH" Diagnostics 11, no. 4: 708.
https://doi.org/10.3390/diagnostics11040708
APA Style
KucharÃk, M., BudiÅ¡, J., Hýblová, M., Minárik, G., & Szemes, T.
(2021). Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH. Diagnostics, 11(4), 708.
https://doi.org/10.3390/diagnostics11040708