Validation of intra- and inter-laboratory reproducibility of the Xpert HPV assay according to the international guidelines for cervical cancer screening-Reference-Cited by-同舟云学术

Validation of intra- and inter-laboratory reproducibility of the Xpert HPV assay according to the international guidelines for cervical cancer screening

Published:2018-10-29 Issue:1 Volume:15 Page:
ISSN:1743-422X
Container-title:Virology Journal
language:en
Short-container-title:Virol J

Author:

Akbari Ajmal,Vanden Broeck Davy^ORCID,Benoy Ina,Padalko Elizaveta,Bogers Johannes,Arbyn Marc

Publisher

Springer Science and Business Media LLC

Subject

Infectious Diseases,Virology

Link

http://link.springer.com/content/pdf/10.1186/s12985-018-1076-6.pdf

Reference10 articles.

1. Arbyn M, Ronco G, Anttila A, et al. Evidence regarding human papillomavirus testing in secondary prevention of cervical cancer. Vaccine. 2012;30(Suppl 5):F88–99.

2. Meijer CJLM, Berkhof H, Heideman DA, Hesselink AT, Snijders PJF. Validation of high-risk HPV tests for primary cervical screening. J Clin Virol. 2009;46:S1–4. https://doi.org/10.1016/S1386-6532(09)00540-X .

3. Arbyn M, Snijders PJF, Meijer CJLM, et al. Which high-risk HPV assays fulfil criteria for use in primary cervical cancer screening? Clin Microbiol Infect. 2015;21:817–26.

4. Micalessi IM, Boulet GA, Bogers JJ, Benoy IH, Depuydt CE. High-throughput detection, genotyping and quantification of the human papillomavirus using real-time PCR. Clin Chem Lab Med. 2012;50(4):655–61.

5. Depuydt CE, Benoy IH, Beert JF, Criel AM, Bogers JJ, Arbyn M. Clinical validation of a type-specific real-time quantitative human papillomavirus PCR against the performance of hybrid capture 2 for the purpose of cervical cancer screening. J Clin Microbiol. 2012;50(12):4073–7.

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