lee2022clinicalStudy of pediatric norovirus gastroenteritis cases admitted to Chang Gung Memorial Hospital (Taiwan) during 2017–2018. Norovirus was quantified from fecal specimens using a SYBR Green-based real-time qRT-PCR method and genotypes were characterized by sequencing. CSV figure data provide norovirus concentrations over days after symptom onset, reported either as gc/mL (many participants) or gc/wet gram (one immunocompromised patient with prolonged shedding).
gc_ml
Norovirus RNA concentration measured by SYBR Green-based real-time quantitative RT-PCR (qRT-PCR) from fecal specimen extract; values reported as gene copies per mL (gc/mL).
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.
gc_wet_gram
Norovirus RNA concentration measured by SYBR Green-based real-time quantitative RT-PCR (qRT-PCR) from stool; values reported as gene copies per wet gram (gc/wet gram).
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.