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Design of a 2D Melting Curve-Based Multiplex PCR Assay for Detection of SARS-CoV-2/RSV/Influenza A-B. [PDF]
Sayan M, Arikan A, Atesoğlu T.
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Application of microfluidic chip-based multiplex PCR in diagnosing reproductive tract pathogens among patients with premature rupture of membranes. [PDF]
Zhang L, Shao Z.
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Multicenter evaluation of fast multiplex PCR for detection of pathogens in lower respiratory tract infections. [PDF]
Wang L +14 more
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Multiplex PCR-based rapid pathogen identification in acute cholecystitis using the FilmArray BCID2 panel. [PDF]
Nakamura G +10 more
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ThermoPlex: an automated design tool for target-specific multiplex PCR primers based on DNA thermodynamics. [PDF]
Agmata A +3 more
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2021
Amplification of different nucleic acid targets in the same reaction (multiplex polymerase chain reaction) is challenging but an extremely useful tool especially for viroid diagnosis. In the amplification mixtures, several pairs of primers work together in the same conditions to detect different targets.
Francesco, Faggioli, Marta, Luigi
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Amplification of different nucleic acid targets in the same reaction (multiplex polymerase chain reaction) is challenging but an extremely useful tool especially for viroid diagnosis. In the amplification mixtures, several pairs of primers work together in the same conditions to detect different targets.
Francesco, Faggioli, Marta, Luigi
openaire +2 more sources
Multiplex PCR Design for Scalable Resequencing
2021While conventional PCR applications typically focus on a single PCR assay per reaction, multiplex PCR applications are a convenient and scalable solution becoming more routine. Multiplex methods can be applied to virtually any DNA template source (e.g., plant or human DNA, FFPE DNA isolated from clinical samples, bisulfite-converted DNA for DNA ...
Korbie, Darren, Trau, Matt
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Multiplex Real-Time PCR (MRT-PCR) for Diarrheagenic
2012Diarrheagenic Escherichia coli strains are important causes of diarrhea in children from the developing world and are now being recognized as emerging enteropathogens in the developed world. Current methods of detection are too expensive and labor-intensive for routine detection of these organisms to be practical.
Barletta, Francesca +2 more
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