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Novel Light Upon Extension Real Time PCR Assays for Detection and Quantification of Genogroup I and II Noroviruses in Clinical Specimens

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Figure

TABLE 1. Primers used for evaluation of the assay conditions with conventional PCR on clinical specimens
TABLE 2. Detection and quantification of NV GI and NV GII inLUX real-time PCR assays on 61 clinical specimensfrom Sweden
TABLE 4. Detection and quantification of norovirus GI and GII inLUX real-time PCR assays on 42 clinical specimens from Nicaragua
FIG. 3. First-derivative dissociation curves. (A) Eight NV GI-positive samples, 10 NV GII-positive samples and 8 negative samples run intriplicates in a duplex real-time PCR assay consisting of both NV GI- and NV GII-specific primer pairs

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