首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Performance Characteristics of the COBAS Amplicor Hepatitis C Virus (HCV) Monitor Version 2.0 International Unit Assay and the National Genetics Institute HCV Superquant Assay
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Performance Characteristics of the COBAS Amplicor Hepatitis C Virus (HCV) Monitor Version 2.0 International Unit Assay and the National Genetics Institute HCV Superquant Assay

机译:COBAS Amplicor丙型肝炎病毒(HCV)监控器2.0版国际单位测定和国家遗传研究所HCV超定量测定的性能特征

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摘要

The COBAS Amplicor Hepatitis C Virus (HCV) Monitor assay, version 2.0, which reports in international units per milliliter, was compared to the assay reported in copies per milliliter by analyzing dilution series and clinical plasma samples by both methods. In addition, the Amplicor international unit assay was compared to the National Genetics Institute HCV Superquant assay. The dilution series ranged from <100 to 5,000,000 HCV RNA copies/ml and consisted of 32 points, assayed in triplicate in each assay. Thirty clinical samples ranging from 1,000 to 1,000,000 HCV RNA copies/ml were assayed in duplicate. Deming regression analysis comparing the Amplicor HCV RNA international units-per-milliliter and copies-per-milliliter assays was calculated as follows: (Amplicor international units per milliliter) = 1.030(Amplicor copies per milliliter) − 0.392; R2 = 0.981; n = 28; Sy/x (standard error of the estimate) = 0.129. The linearity of the Amplicor international units-per-milliliter assay was as follows: observed = 0.886(expected) + 0.437; R2 = 0.983; n = 30. The linearity of the Superquant assay was as follows: observed= 0.918 (expected) + 0.436; R2 = 0.986; n = 32. Deming regression analysis comparing the Amplicor and Superquant assays was calculated as follows: Superquant = 1.066(Amplicor) − 0.0197; R2 = 0.908; Sy/x = 0.308; n = 28. The Amplicor and Superquant assays were linear through the range of 600 to 600,000 IU of HCV RNA/ml and ∼300 to 5,000,000 HCV RNA copies/ml, respectively. The narrow range of the Amplicor assay means that some samples will require dilution and retesting for accurate quantification above 600,000 IU of HCV RNA/ml. The Amplicor and Superquant assays agreed well within the range of 600 to 600,000 IU of HCV RNA/ml (∼1,000 to ∼1,000,000 HCV RNA copies/ml). Overall, the Amplicor and Superquant assays agree well, and results obtained in one assay could be expected to compare well with results from the other when reported in copies per milliliter.
机译:通过两种方法分析稀释系列和临床血浆样本,将以国际单位每毫升报告的COBAS Amplicor丙型肝炎病毒(HCV)监测器测定法2.0版与以每毫升拷贝数报告的测定法进行了比较。此外,将Amplicor国际单​​位测定与国家遗传研究所HCV Superquant测定进行了比较。稀释系列的范围从<100到5,000,000 HCV RNA拷贝/ ml,由32个点组成,每个测定一式三份。一式两份测定30种临床样品,每份样品的浓度从1,000到1,000,000 HCV RNA拷贝。 Deming回归分析比较Amplicor HCV RNA国际单位毫升数和每毫升单位拷贝数的计算方法如下:(每毫升国际单位扩增子)= 1.030(每毫升国际单位拷贝数)-0.392; R 2 = 0.981; n = 28; Sy / x(估算的标准误差)= 0.129。 Amplicor国际单​​位每毫升分析的线性如下:观察= 0.886(预期)+ 0.437; R 2 = 0.983; n = 30。Superquant测定法的线性如下:观察到= 0.918(预期)+0.436; n = 30。 R 2 = 0.986; n =32。比较Amplicor和Superquant分析的Deming回归分析计算如下:Superquant = 1.066(Amplicor)-0.0197; R 2 = 0.908; Sy / x = 0.308; n =28。Amplicor和Superquant分析分别在600至600,000 IU HCV RNA / ml和约300至5,000,000 HCV RNA拷贝/ ml范围内呈线性关系。 Amplicor测定法的狭窄范围意味着某些样品需要稀释并重新测试才能对HCV RNA / ml超过600,000 IU进行准确定量。在600至600,000 IU HCV RNA / ml(约1,000至约1,000,000 HCV RNA拷贝/ ml)的范围内,Amplicor和Superquant分析的一致性很好。总体而言,Amplicor和Superquant分析方法吻合良好,当以每毫升拷贝数报告时,一种分析方法获得的结果可与另一种分析结果很好地比较。

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