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1 idation included determination of intra- and interassay accuracy and precision values, recovery studi
2 oncentration range of 0.2-200 ng/mL, and the interassay accuracy, intraassay precision, and interassa
5 ble to detect more genotypes per sample, the interassay agreement was acceptable (kappa = 0.53, 63% a
11 pecificity, but lack of standardization, and interassay and interlaboratory variation makes it diffic
14 The cRMP is highly precise with intra-assay, interassay, and total percent CVs of 2.7%, 1.3%, and 2.4
16 mpetitive enzyme-linked immunosorbent assay (interassay coefficient of variation < or = 10%) and comp
17 is also simple to use, has a relatively low interassay coefficient of variation (<6%), retains its p
18 uminex assay was precise, with an intra- and interassay coefficient of variation 8.1% and 9.3%; showe
19 ad a <10% interassay relative error and <15% interassay coefficient of variation across a range from
21 TS13-depleted plasma resulting in an average interassay coefficient of variation of 7.1% and a limit
28 ize BKV NAAT results, we anticipate improved interassay comparisons with a potential for establishing
31 ellent agreement between the assays, with an interassay concordance of 91.35% (kappa = 0.75; 95% conf
33 y coefficient of variation (CV) of 4% and an interassay CV of 6% obtained from seven studies, enablin
36 The sensor had excellent precision (1.9-8.2% interassay CV) and was comparable in performance to comm
37 rformance to single-analyte ELISAs (1.9-8.1% interassay CV; <2 ng/mL (or units/mL) detection limit fo
38 and reproducibility (serum assay, intra- and interassay CVs < 3% and ICCs > 99%; urine assay, intra-a
39 fficients of variation [CVs], 0.8%, and mean interassay CVs, 1.6%) and rapid (3.5 min per assay) and
43 Accuracy was >or=85.7% with intra-assay and interassay imprecision<or=13.9 and 12.4%, respectively.
48 terassay accuracy, intraassay precision, and interassay precision do not exceed 8.6%, 12%, and 12%, r
50 n of < or =2.5% coefficient of variation and interassay precision of < or =4.0% coefficient of variat
52 The coefficients of variation for intra- and interassay precision were less than 9 and 14%, respectiv
53 lidation results were as follows: intra- and interassay precision with %CV of 8.2-9.9 and 7.1-9.8%, r
54 specimen dilution, good clinical intra- and interassay precision, and excellent correlation with the
55 cimens for linearity, intra-assay precision, interassay precision, limit of detection, and specificit
58 alyzed separately, but this fails to capture interassay relationships, making multiassay biomarker di
60 s per reaction mixture, (vi) high intra- and interassay reproducibilities, and (vii) correct identifi
62 se at concentrations down to 58.8 fM with an interassay reproducibility (%RSD of n = 3) < 17.2%, and
63 orphometric techniques had good to excellent interassay reproducibility (R(2) = 0.62 to 0.96) and int
66 erent levels of methylation showed excellent interassay reproducibility of RSD (relative standard dev
68 ty was found to be between 2.5 and 12.3% and interassay reproducibility was between 6.1 and 15.2% for
69 een the assays (R(2) = 0.99); the intra- and interassay reproducibility was excellent overall (SD = 0
71 es are quantitative for all nucleotides, and interassay variabilities are between 5 and 7% when quant
73 The estimated standard deviations including interassay variability and intra-assay variability of th
75 ys are especially subject to high intra- and interassay variability because they are not subject to m
76 btained by chemical synthesis, an intra- and interassay variability below 8% and an accuracy of 92% t
78 cients (ICCs) between antibodies to quantify interassay variability for PD-L1 expression in tumor cel
80 ntly improved amplification specificity, and interassay variability is comparable to that of commerci
83 earity, specificity, sensitivity, intra- and interassay variability, and robustness to sample storage
84 peatability (RSDr = 6% and 9% for intra- and interassay variability, respectively) and specificity: o
90 s very accurate and precise, with intra- and interassay variations of less than 3% when 5 microg of p