An Efficient and User-Friendly Software for PCR Primer Design for Detection of Highly Variable Bacteria
Author:
Publisher
Springer Nature Switzerland
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-23198-8_13
Reference19 articles.
1. Ling, T.K., Xiong, J., Yu, Y., Lee, C.C., Ye, H., Hawkey, P.M.: Multicenter antimicrobial susceptibility survey of gram-negative bacteria isolated from patients with community-acquired infections in the People’s Republic of China. Antimicrob Agents Chemother 50(1), 374–378 (2006)
2. Conter, C.C., et al.: PCR primers designed for new world Leishmania: a systematic review. Exp. Parasitol. 207, 107773 (2019)
3. Bui, T.H., et al.: Multiplex PCR method for differentiating highly pathogenic Yersinia enterocolitica and low pathogenic Yersinia enterocolitica, and Yersinia pseudotuberculosis. J. Vet. Med. Sci. 83(12), 1982–1987 (2021)
4. Bouju-Albert, A., Saltaji, S., Dousset, X., Prévost, H., Jaffrès, E.: Quantification of Viable Brochothrix thermosphacta in Cold-Smoked Salmon Using PMA/PMAxx-qPCR. Front Microbiol 12, 654178 (2021)
5. Wang, K., et al.: MFEprimer-3.0: quality control for PCR primers. Nucleic Acids Res. 47(1),W610–W613 (2019)
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