Rimmer, A., Phan, H., Mathieson, I., Iqbal, Z., Twigg, S. R. F., Wilkie, A. O. M., . . . Lunter, G. (2014). Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications. Nat Genet.
Citação norma ChicagoRimmer, Andy, Hang Phan, Iain Mathieson, Zamin Iqbal, Stephen R F. Twigg, Andrew O M. Wilkie, Gil McVean, and Gerton Lunter. "Integrating Mapping-, Assembly- and Haplotype-based Approaches for Calling Variants in Clinical Sequencing Applications." Nat Genet 2014.
MLA citiranjeRimmer, Andy, et al. "Integrating Mapping-, Assembly- and Haplotype-based Approaches for Calling Variants in Clinical Sequencing Applications." Nat Genet 2014.
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