{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,6]],"date-time":"2026-01-06T02:22:56Z","timestamp":1767666176120},"reference-count":12,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2012,6,18]],"date-time":"2012-06-18T00:00:00Z","timestamp":1339977600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Medical Virology"],"published-print":{"date-parts":[[2012,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>This study was conducted to evaluate the overall performance of a reverse blot hybridization\u2010based assay, REBA HPV\u2010ID\u00ae (Molecules and Diagnostics, Wonju, Korea) for genotyping human papillomaviruses (HPV). HPV Genotyping on 356 specimens examined cytologically was performed using the REBA HPV\u2010ID\u00ae, and its results were compared with those obtained using the MyHPV DNA Chip\u00ae (Mygene, Seoul, Korea), DNA chip\u2010based HPV genotyping assay. The results from this study showed that the positivity rate of the REBA HPV\u2010ID\u00ae for abnormal cytological samples was higher (80.9%) than that of the MyHPV DNA chip (69.8%). In addition, the REBA HPV\u2010ID\u00ae positivity rate with normal cytological samples was higher (64.4%) than that obtained using DNA chips (34.4%). Subsequently, sequence analysis was performed with specimens that generated conflicting test results. Sequence analysis confirmed that the specimens which were positive by REBA HPV\u2010ID\u00ae did indeed contain HPV sequences. The results of this study suggest that the REBA HPV\u2010ID\u00ae is a sensitive test for genotyping HPV of clinical specimens. J. Med. 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