Koboldt, D. C. (2020). Best practices for variant calling in clinical sequencing. Genome Med.
Dyfyniad Arddull ChicagoKoboldt, Daniel C. "Best Practices for Variant Calling in Clinical Sequencing." Genome Med 2020.
Dyfyniad MLAKoboldt, Daniel C. "Best Practices for Variant Calling in Clinical Sequencing." Genome Med 2020.
Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.