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Rapid and sensitive detection of Little cherry virus 2 using isothermal reverse transcription- RPA

RT-RPA and lateral flow used to detect the Little cherry virus 2 coat protein gene. RT-RPA was simple, fast, and specific. The test has the sensitivity of RT-PCR and is more cost effective, being capable of detecting the virus from crude extracts from field samples.

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Rapid detection of Schmallenberg Virus & Bovine Viral Diarrhoea Virus using isothermal amplification

Among a wide range of available technologies, high-speed real-time reverse transcriptase quantitative PCR (RT-qPCR) and the two isothermal amplification techniques loop-mediated isothermal amplification (LAMP) and recombinase polymerase amplification (RPA) represent three promising candidates for integration into mobile pen-side tests.

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Rapid Molecular Assays for the Detection of Yellow Fever Virus in Low-Resource Settings

RPA assays were developed to detect Yellow Fever Virus on three different platforms (real-time with or without microfluidic semi-automated system and lateral-flow assay). The assay was able to detect 20 different YFV strains with no cross-reactions with closely related viruses. The RPA assay proved to be a robust, portable method with a low detection limit (

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