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Average accuracy of assay of moxifloxacin and cefixime were found to be 100.68% and 9893%%, respectively.
This was largely due to the improvement in sensitivity and accuracy of assay with the new method, which resulted in a decrease in the normal value in healthy controls.
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Precision and accuracy of assays were confirmed using standard quality controls (Precinorm Clin Chem Multi 1 and 2, Roche Diagnostics).
Further, recent infection testing algorithms using a multiple incidence assays in combination with additional clinical (e.g., CD4 cell count, RNA testing), laboratory (e.g., ART testing), and historical information should be explored for improving the accuracy of assay-derived incidence estimates.
This finding could be attributed to early infection, transient intestinal virus passage, or low accuracy of assays used (14 ).
Moreover, lack of a clearly defined number of T cells specific for a defined antigen within each aliquot hampers the assessment of the accuracy of assays applied.
The accuracy of assaying PKB activation by immunohistochemical analysis using antibody against the phosphorylated active form of PKB has not been definitively established.
The accuracy of the assay was validated by comparison to a radioactive ATPase assay (Supplementary Figure S3).
Inter- and intra-assay coefficients of variance were calculated in order to determine the accuracy of the assay.
Because this digital assay does not rely on internal or external standards, the RSD of approximately 3.0% demonstrates the true accuracy of the assay.
The results for precision and accuracy of the assay are summarised in Table 3.
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