Sequencing and Resolution of Amplified Herpes Simplex Virus DNA with Intermediate Melting Curves as Genotype 1 or 2 by LightCycler PCR Assay
Author:
Affiliation:
1. AIDS Healthcare Foundation, Jacksonville, Florida 32204
2. Division of Clinical Microbiology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.43.4.1843-1845.2005
Reference10 articles.
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2. Burrows, J., A. Nitsche, B. Bayly, E. Walker, G. Higgins, and T. Kok. 2002. Detection and subtyping of herpes simplex virus in clinical samples by LightCycler PCR, enzyme immunoassay and cell culture. BMC Microbiol.2:12.
3. Diagnosis of Herpes Simplex Virus Infections in the Clinical Laboratory by LightCycler PCR
4. Koenig, M., K. S. Reynolds, W. Aldous, and M. Hickman. 2001. Comparison of LightCycler PCR, enzyme immunoassay, and tissue culture for detection of herpes simplex virus. Diagn. Microbiol. Infect. Dis.40:107-110.
5. Smith, T. F., M. J. Espy, and M. F. Jones. 2004. Molecular virology: current and future trends, p. 543-548. D. H. Persing, F. C. Tenover, J. Versalovic, Y. W. Tang, E. R. Unger, D. A. Relman, and T. J. White (ed.), Molecular microbiology diagnostic principles and practice. ASM Press, Washington, D.C.
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