“…All HPV testing will be performed using the clinically validated and Federal Drug Agency-approved Cobas 4800 DNA test (Roche Diagnostics, Switzerland), 45 as this is the routine test platform used in the CDR. The test is an automated real-time PCR-based test designed to detect high-risk HPV types: 16,18,31,33,35,39,45,51,52,56,58,59, 66 and 68 45 46 and is validated for use on SurePath collected samples. 47 Results will be reported as (1) HPV negative, (2) HPV positive (HPV16, HPV18 and/ or other HPV types) or (3) invalid.…”