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About:
A multiplex real-time PCR panel assay for simultaneous detection and differentiation of 12 common swine viruses
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
A multiplex real-time PCR panel assay for simultaneous detection and differentiation of 12 common swine viruses
Creator
Bai, Jianfa
Das, Amaresh
Shi, Jishu
Liu, Xuming
Peddireddi, Lalitha
Anderson, Gary
Jia, Wei
Liu, Yanhua
Ma, Guiping
Shi, Xiju
Sun, Qing
Wang, Qin
Xu, Lu
Source
Elsevier; Medline; PMC
abstract
Mixed infection with different pathogens is common in swine production systems especially under intensive production conditions. Quick and accurate detection and differentiation of different pathogens are necessary for epidemiological surveillance, disease management and import and export controls. In this study, we developed and validated a panel of multiplex real-time PCR/RT-PCR assays composed of four subpanels, each detects three common swine pathogens. The panel detects 12 viruses or viral serotypes, namely, VSV-IN, VSV-NJ, SVDV, CSFV, ASFV, FMDV, PCV2, PPV, PRV, PRRSV-NA, PRRSV-EU and SIV. Correlation coefficients (R(2)) and PCR amplification efficiencies of all singular and triplex real-time PCR reactions are within the acceptable range. Comparison between singular and triplex real-time PCR assays of each subpanel indicates that there is no significant interference on assay sensitivities caused by multiplexing. Specificity tests on 226 target clinical samples or 4 viral strains and 91 non-target clinical samples revealed that the real-time PCR panel is 100% specific, and there is no cross amplification observed. The limit of detection of each triplex real-time PCR is less than 10 copies per reaction for DNA, and less than 16 copies per reaction for RNA viruses. The newly developed multiplex real-time PCR panel also detected different combinations of co-infections as confirmed by other means of detections.
has issue date
2016-08-06
(
xsd:dateTime
)
bibo:doi
10.1016/j.jviromet.2016.08.005
bibo:pmid
27506582
has license
no-cc
sha1sum (hex)
633ee9755d994f4e6f4515a40b507dd81cb17811
schema:url
https://doi.org/10.1016/j.jviromet.2016.08.005
resource representing a document's title
A multiplex real-time PCR panel assay for simultaneous detection and differentiation of 12 common swine viruses
has PubMed Central identifier
PMC7119729
has PubMed identifier
27506582
schema:publication
J Virol Methods
resource representing a document's body
covid:633ee9755d994f4e6f4515a40b507dd81cb17811#body_text
is
schema:about
of
named entity 'specific'
named entity 'assays'
named entity 'Comparison'
named entity 'real-time PCR'
named entity 'copies'
named entity 'multiplex'
named entity 'disease management'
named entity 'pathogens'
named entity 'reactions'
named entity 'MEANS'
named entity 'PCV2'
named entity 'IMPORT AND EXPORT'
named entity 'REAL-TIME PCR '
named entity 'RNA VIRUSES'
named entity 'FMDV'
named entity 'DNA'
named entity 'AMPLIFICATION'
named entity 'ACCURATE'
named entity 'ACCEPTABLE'
named entity 'QUICK'
named entity 'CLINICAL'
named entity 'REACTIONS'
named entity 'INTERFERENCE'
named entity 'STUDY'
covid:arg/633ee9755d994f4e6f4515a40b507dd81cb17811
named entity 'ASFV'
named entity 'TARGET'
named entity 'EFFICIENCIES'
named entity 'DETECTED'
named entity 'PANEL'
named entity 'PATHOGENS'
named entity 'COMBINATIONS'
named entity 'COMPARISON'
named entity 'COMMON'
named entity 'NEWLY'
named entity 'MULTIPLEXING'
named entity 'PCR'
named entity 'CONFIRMED BY'
named entity 'OF EACH'
named entity '226'
named entity 'CORRELATION'
named entity 'NECESSARY'
named entity 'LESS THAN'
named entity 'LIMIT OF DETECTION'
named entity 'PRV'
named entity 'PRODUCTION'
named entity 'NON-TARGET'
named entity 'MULTIPLEX REAL-TIME PCR'
named entity 'REAL-TIME PCR '
named entity 'COMMON'
named entity 'ASSAY'
named entity 'SEROTYPES'
named entity 'TESTS'
named entity 'DETECTION'
named entity 'COMPOSED OF'
named entity 'REACTION'
named entity '100%'
named entity 'VIRUSES'
named entity 'ASSAY'
named entity 'DIFFERENTIATION'
named entity 'RANGE'
named entity 'REVEALED'
named entity 'VSV'
named entity 'SAMPLES'
named entity 'SYSTEMS'
named entity 'CONDITIONS'
named entity 'SURVEILLANCE'
named entity 'MIXED INFECTION'
named entity 'PANEL'
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