Résultats de la recherche - 4 results
Validation of intra- and inter-laboratory reproducibility of the Xpert HPV assay according to the international guidelines for cervical cancer screening.
intra- and inter-laboratory agreement regarding detection of high-risk HPV DNA exceeding 87% with kappa ≥0.5. RESULTS The Xpert HPV assay showed high intra-laboratory reproducibility with an overall ...
Performance of a Cartridge-Based Assay for Detection of Clinically Significant Human Papillomavirus (HPV) Infection: Lessons from VALGENT (Validation of HPV Genotyping Tests).
HPV were 98% and 97%, respectively. The kappa agreements for HPV16 and HPV18 /45 between the clinically validated reference test (GP5 +/6+ LMNX) and the Xpert HPV were 0.92 and 0.91, respectively. The ...
Direct comparison of two vaginal self-sampling devices for the detection of human papillomavirus infections.
rates between self-collected and clinician-collected specimens (Evalyn: 91.2% [kappa 0.822]; Qvintip: 89.0% [kappa 0.779]). Colposcopy and histological evaluation revealed 55 women without cervical ...
Clinical and Analytical Performance of the Onclarity HPV Assay Using the VALGENT Framework.
a relative specificity of 0.99 (95% CI, 0.97 to 1.00; P = 0.186 for noninferiority). The kappa for agreement between the Onclarity assay and the GP5+/6+ LMNX assay for HR-HPV was 0.92 (95% CI, 0.89 to 0.94), ...