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The aim of this study was to establish a fast and reliable molecular method for identification and differentiation.
qPCR is now increasingly being used as a molecular method for enumerating bacterial load in complex microbiota like rumen (Klieve et al. 2003; Tajima et al. 2001).
The purpose of this study was to develop a simple, rapid and reliable molecular method for specific authentication of seahorse species.
Therefore, a molecular method for identification of S. Weltevreden in clinical isolates based on amplification of a specific DNA sequence present in its genome is proposed.
Nucleic acid sequence-based amplification (NASBA) is a molecular method for amplification of target RNA segments in which the necessity of thermo cycling is excluded due to lack of any thermal variation in the reaction environment.
Quantitative PCR (qPCR) is the standard molecular method for detection of polyomavirus JC (JCPyV) DNA reactivation in serum and cerebrospinal fluid (CSF) in patients at risk of progressive multifocal leukoencephalopathy (PML).
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Molecular methods for subtyping isolates are necessary for allowing epidemiological surveillance and control of eradication programs.
Results and conclusion: Serological methods and molecular methods for the detection and quantitation of HIV are discussed.
The aim of this study was to improve molecular methods for the detection of bovine viral diarrhoea virus (BVDV).
The application of molecular methods for the epidemiology of TB complement traditional approaches used in public health.
Our case also highlights the diagnostic role of molecular methods for these infections in routine laboratories for rapid management and better patient outcome.
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