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    Facile, comprehensive, high-throughput genotyping of human genital papillomaviruses using spectrally addressable liquid bead microarrays

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    Authors
    Wallace, Jan
    Woda, Bruce A.
    Pihan, German A.
    UMass Chan Affiliations
    Department of Pathology
    Laboratory of Diagnostic Molecular Oncology
    Document Type
    Journal Article
    Publication Date
    2005-02-01
    Keywords
    DNA, Viral
    Female
    Genotype
    Humans
    Microspheres
    Oligonucleotide Array Sequence Analysis
    Papillomaviridae
    Papillomavirus Infections
    Polymerase Chain Reaction
    Uterine Cervical Neoplasms
    Life Sciences
    Medicine and Health Sciences
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    Link to Full Text
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867512/?tool=pubmed
    Abstract
    Human papillomavirus (HPV) is the worldwide cause of carcinoma of the uterine cervix, a cancer that is the second most common neoplasm in women, resulting in nearly 250,000 deaths a year. The magnitude of the risk of cancer after HPV infection, however, is virus type-specific. Over 40 HPV types can infect the genital tract. Comprehensive, high-throughput typing assays for HPV, however, are not currently available. Blending multiplex PCR and multiplex hybridization using spectrally addressable liquid bead microarrays we have developed a high-throughput, fast, single-tube-typing assay capable of simultaneously typing 45 HPV. The overall incidence of HPV in 429 women tested using this new assay was 72.2% for those with squamous intraepithelial lesions, 51.5% for those with atypical squamous cells of undetermined significance and 15.4% for women with normal cytology, respectively. This compared well with the incidence of HPV detected by a parallel non-typing generic high-risk assay. The new assay detected a wide spectrum of HPV types and a high incidence of mixed infections. We believe our assay may find widespread applications in areas requiring virus type-specific information, such as in epidemiological studies, cancer screening programs, monitoring therapeutic interventions, and evaluating the efficacy of HPV vaccine trials.
    Source
    J Mol Diagn. 2005 Feb;7(1):72-80.
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/38285
    PubMed ID
    15681477
    Related Resources
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    UMass Chan Faculty and Researcher Publications

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