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HBV Drug Resistance Typing EQA/PT Scheme
To assess the performance of laboratories in the detection of drug resistance mutations in the hepatitis B virus (HBV) DNA polymerase gene using sequencing techniques and/or LiPA technology.
Total Number of Challenges: 1
Number of Panel Members: 4
Distribution / Testing Period: Q3
| Sample NA Target Source | Cultured and/or Clinical material |
| Matrix Panel Format | Plasma |
| Panel Member Target Range | Various mutations – DNA polymerase |
| Panel Member Sample Volume | 1.0 ml |
| Panel Sample Pre-treatment Requirement | Ready for analysis. Treat as clinical samples and analyse accordingly. |
| Panel Analysis Type | Sequence Analysis |
| Panel Testing | Evaluated by various molecular methodologies |
| Storage / Shipment Conditions | <-20°C / Frozen on Dry-ice |
| Accreditation / Regulatory Status | Accredited to ISO 17043 |
$1,426.53
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