Multiplex real-time PCR for SARS-CoV-2, influenza A/B and RSV: analytical and clinical evaluation
Journal of Clinical Virology (PMC) · 2021
Curated peer-reviewed / authoritative reference. Open the source link for the full text.
Real-time fluorescence-monitored amplification enabling rapid detection and, with appropriate calibration, quantitative measurement of pathogen load.
qPCR adds quantification to speed: monitoring fluorescence each cycle allows both rapid detection and measurement of pathogen load — critical for monitoring viral infections such as CMV and EBV in transplant patients.
Specimen requirements: data to be updated. Please contact ID Labs.
Container information: data to be updated.
Validated target list: data to be updated. Please contact ID Labs for the current configuration.
| Characteristic | Value | Source |
|---|---|---|
| Analytical / clinical performance | Performance characteristics: please contact ID Labs — data to be updated. | ID Labs Validated Performance |
Qualitative detection where speed matters, and quantitative monitoring (viral load) where calibrated. Simultaneous analysis of hundreds of samples with a high degree of analytical precision.
Journal of Clinical Virology (PMC) · 2021
Curated peer-reviewed / authoritative reference. Open the source link for the full text.
PMC (peer-reviewed review) · 2024
Curated peer-reviewed / authoritative reference. Open the source link for the full text.
Targeted amplification of pathogen DNA for sensitive, specific qualitative detection of infectious agents.
The reference molecular approach for RNA viruses: reverse transcription of RNA into cDNA followed by amplification and detection.
Panel configuration, specimen logistics and turnaround details on request.
Information on this page is educational and does not replace professional clinical judgment. Performance values are labelled by source (ID Labs Specification / ID Labs Validated Performance / Manufacturer Specification / Published Scientific Evidence). Molecular results must be correlated clinically and, where appropriate, confirmed by culture and phenotypic susceptibility testing.