<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(11)</volume><submitter>He A</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Human papillomavirus (HPV) 6 and 11 are the two most common low-risk HPV subtypes, accounting for more than 90% of condyloma acuminatum. A simple, accurate and rapid screening method to be applied in community-level hospitals is in high demand.&lt;h4>Methods&lt;/h4>Endogenous internally controlled recombinase-assisted amplification (EIC-RAA) assays for HPV6 and 11 were performed in a single closed-tube at 39 °C within 30 min. The sensitivity and specificity of EIC-RAA were examined using recombinant plasmids and pre-tested HPV DNA. A total of 233 clinical samples were collected, and the DNA was extracted by traditional multi-step extraction, or sample releasing agent, before analysis by EIC-RAA. For comparison, HPV detection via Quantitative real-time PCR (qPCR) was also perfor</pubmed_abstract><journal>Heliyon</journal><pagination>e11323</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9647352</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of field-applicable endogenous internally controlled recombinase-aided amplification (EIC-RAA) assays for the detection of human papillomavirus genotypes 6 and 11 using sample releasing agent.</pubmed_title><pmcid>PMC9647352</pmcid><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Tan H</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Fang C</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Nie M</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Ming Y</pubmed_authors><pubmed_authors>Rong X</pubmed_authors><pubmed_authors>He A</pubmed_authors><pubmed_authors>Shen X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of field-applicable endogenous internally controlled recombinase-aided amplification (EIC-RAA) assays for the detection of human papillomavirus genotypes 6 and 11 using sample releasing agent.</name><description>&lt;h4>Objective&lt;/h4>Human papillomavirus (HPV) 6 and 11 are the two most common low-risk HPV subtypes, accounting for more than 90% of condyloma acuminatum. A simple, accurate and rapid screening method to be applied in community-level hospitals is in high demand.&lt;h4>Methods&lt;/h4>Endogenous internally controlled recombinase-assisted amplification (EIC-RAA) assays for HPV6 and 11 were performed in a single closed-tube at 39 °C within 30 min. The sensitivity and specificity of EIC-RAA were examined using recombinant plasmids and pre-tested HPV DNA. A total of 233 clinical samples were collected, and the DNA was extracted by traditional multi-step extraction, or sample releasing agent, before analysis by EIC-RAA. For comparison, HPV detection via Quantitative real-time PCR (qPCR) was also perfor</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-05-31T23:10:52.803Z</modification><creation>2024-10-17T17:11:01.768Z</creation></dates><accession>S-EPMC9647352</accession><cross_references><pubmed>36387484</pubmed><doi>10.1016/j.heliyon.2022.e11323</doi></cross_references></HashMap>