Characterization of microbial pathogens is necessary for surveillance, outbreak detection, and tracing of outbreak sources. This unit describes a multiplex oligonucleotide ligation-PCR (MOL-PCR) optimized for characterization of microbial pathogens. With MOL-PCR, different types of markers, like unique sequences, single-nucleotide polymorphisms (SNPs) and indels, can be simultaneously analyzed in one assay. This assay consists of a multiplex ligation for detection of the markers, a singleplex PCR for signal amplification, and hybridization to MagPlex-TAG beads for readout on a Luminex platform after fluorescent staining. The current protocol describes the MOL-PCR, as well as methods for DNA isolation, probe design, and data interpretation a...
<p>A. Three oligonucleotides and two fluorescently labelled beads are used for interrogation of one ...
A proof of principle of a multi-target assay for genotyping Salmonella has been developed targeting ...
An optimized multiplex-polymerase chain reaction (m-PeR) assay has been developed using novel genes ...
Characterization of microbial pathogens is necessary for surveillance, outbreak detection, and traci...
<p>Characterization of microbial pathogens is necessary for surveillance, outbreak detection, ...
<p>With multiplex oligonucleotide ligation-PCR (MOL-PCR) different molecular markers can be si...
A multiplex oligonucleotide ligation-PCR (MOL-PCR) assay is a valuable high-throughput technique for...
<p>A multiplex oligonucleotide ligation-PCR (MOL-PCR) assay is a valuable high-throughput tech...
With multiplex oligonucleotide ligation-PCR (MOL-PCR) different molecular markers can be simultaneou...
Copyright © 2015 Véronique Wuyts et al. This is an open access article distributed under the Creati...
Multiplex oligonucleotide ligation-PCR (MOL-PCR) is a rapid method for simultaneous detection of mul...
Subtyping below the serovar level is essential for surveillance and outbreak detection and investiga...
Abstract Subtyping below the serovar level is essential for surveillance and outbreak detection and ...
Abstract Subtyping below the serovar level is essential for surveillance and outbreak detection and ...
Salmonellosis outbreaks involving typhoid fever and human gastroenteritis are important diseases in ...
<p>A. Three oligonucleotides and two fluorescently labelled beads are used for interrogation of one ...
A proof of principle of a multi-target assay for genotyping Salmonella has been developed targeting ...
An optimized multiplex-polymerase chain reaction (m-PeR) assay has been developed using novel genes ...
Characterization of microbial pathogens is necessary for surveillance, outbreak detection, and traci...
<p>Characterization of microbial pathogens is necessary for surveillance, outbreak detection, ...
<p>With multiplex oligonucleotide ligation-PCR (MOL-PCR) different molecular markers can be si...
A multiplex oligonucleotide ligation-PCR (MOL-PCR) assay is a valuable high-throughput technique for...
<p>A multiplex oligonucleotide ligation-PCR (MOL-PCR) assay is a valuable high-throughput tech...
With multiplex oligonucleotide ligation-PCR (MOL-PCR) different molecular markers can be simultaneou...
Copyright © 2015 Véronique Wuyts et al. This is an open access article distributed under the Creati...
Multiplex oligonucleotide ligation-PCR (MOL-PCR) is a rapid method for simultaneous detection of mul...
Subtyping below the serovar level is essential for surveillance and outbreak detection and investiga...
Abstract Subtyping below the serovar level is essential for surveillance and outbreak detection and ...
Abstract Subtyping below the serovar level is essential for surveillance and outbreak detection and ...
Salmonellosis outbreaks involving typhoid fever and human gastroenteritis are important diseases in ...
<p>A. Three oligonucleotides and two fluorescently labelled beads are used for interrogation of one ...
A proof of principle of a multi-target assay for genotyping Salmonella has been developed targeting ...
An optimized multiplex-polymerase chain reaction (m-PeR) assay has been developed using novel genes ...