Validation of Novaprep® HQ+ liquid-based cytology medium for high-risk human papillomavirus detection by hc2
Résumé
Preanalytical conditions determine the reliability and validity of bioassays. Therefore, the analytic performances of biological tests need to be determined when preanalytical steps differ from those recommended by the manufacturer. The objective of the study was to assess the analytic performance of the hc2 test for the detection of high-risk HPV DNA from cells stored in the new Novaprep® HQ+ medium.
Domaines
CancerOrigine | Publication financée par une institution |
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