pombubpa2012assessmentEvaluation study in Thailand assessing the commercial immunochromatographic assay RIDA® QUICK Norovirus for detection of norovirus in stool from patients with acute gastroenteritis, using RT-PCR/quantitative real-time RT-PCR as reference. CSV-provided data include quantitative norovirus concentrations for individual patients and genogroups (GI or GII) at specified days after a reference event (not specified in provided text/CSV).
gii
Quantitative norovirus genogroup II (GII) measurement in stool by commercial quantitative real-time RT-PCR (as referenced in the abstract) used to compare with RIDA® QUICK Norovirus immunochromatographic assay performance.
Measurements only — no shedding model is fitted to this analyte, usually because it is sampled once per participant, leaving no trajectory to fit, or because nothing was ever detected. Open triangles are non-detects, drawn at the assay's censoring limit. See the modelling methods for what these estimates do and do not support.
gi
Quantitative norovirus genogroup I (GI) measurement in stool by commercial quantitative real-time RT-PCR (as referenced in the abstract) used to compare with RIDA® QUICK Norovirus immunochromatographic assay performance.
Measurements only — no shedding model is fitted to this analyte, usually because it is sampled once per participant, leaving no trajectory to fit, or because nothing was ever detected. Open triangles are non-detects, drawn at the assay's censoring limit. See the modelling methods for what these estimates do and do not support.