摘要
Abstract
Objective To explore the indoor quality controlproblems in HBV DNA quantitative detection of real-time fluorescence quantitative PCR. Indoor quality control serum HBsAg positive self detection.Methods For 1~7 months of 2013 by real-time fluorescence quantitativePCR method and clinical specimens, synchronous detection, curve of standard logarithm, calculated for eachpositive quality control results of the slope, intercept and correlation coefficient (R) value and related results ,standard deviation (s) and the coefficient of variation(CV), scat er picture quality control chart for quality control by using the EXCEL line. Results The 1~7 months of 2013 were positive results of internal quality control of homemade measured values are in control, the standard deviation and variation coefficient were within the al owable range, meet the requirements. Conclusion This laboratory detection of HBV-DNA quantitative real-time fluorescence quantitative PCR detection process,quality control methods and quality control of homemadegood stability, can provide valid and reliable accurate test results for clinical.关键词
实时荧光定量/聚合酶链反应/HBV-DNA/室内质控Key words
Real time fluorescence quantitative PCR/Polymerase chain reaction/HBV-DNA/Quality control