Please use this identifier to cite or link to this item: https://doi.org/10.1093/nar/gkq089
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dc.titleLarge-scale evolutionary surveillance of the 2009 H1N1 influenza A virus using resequencing arrays
dc.contributor.authorLee, C.W.H.
dc.contributor.authorKoh, C.W.
dc.contributor.authorChan, Y.S.
dc.contributor.authorAw, P.P.K.
dc.contributor.authorLoh, K.H.
dc.contributor.authorHan, B.L.
dc.contributor.authorThien, P.L.
dc.contributor.authorNai, G.Y.W.
dc.contributor.authorHibberd, M.L.
dc.contributor.authorWong, C.W.
dc.contributor.authorSung, W.-K.
dc.date.accessioned2013-07-04T07:29:28Z
dc.date.available2013-07-04T07:29:28Z
dc.date.issued2010
dc.identifier.citationLee, C.W.H., Koh, C.W., Chan, Y.S., Aw, P.P.K., Loh, K.H., Han, B.L., Thien, P.L., Nai, G.Y.W., Hibberd, M.L., Wong, C.W., Sung, W.-K. (2010). Large-scale evolutionary surveillance of the 2009 H1N1 influenza A virus using resequencing arrays. Nucleic Acids Research 38 (9) : e111-e111. ScholarBank@NUS Repository. https://doi.org/10.1093/nar/gkq089
dc.identifier.issn03051048
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/38902
dc.description.abstractIn April 2009, a new influenza A (H1N1 2009) virus emerged that rapidly spread around the world. While current variants of this virus have caused widespread disease, particularly in vulnerable groups, there remains the possibility that future variants may cause increased virulence, drug resistance or vaccine escape. Early detection of these virus variants may offer the chance for increased containment and potentially prevention of the virus spread. We have developed and field-tested a resequencing kit that is capable of interrogating all eight segments of the 2009 influenza A(H1N1) virus genome and its variants, with added focus on critical regions such as drug-binding sites, structural components and mutation hotspots. The accompanying base-calling software (EvolSTAR) introduces novel methods that utilize neighbourhood hybridization intensity profiles and substitution bias of probes on the microarray for mutation confirmation and recovery of ambiguous base queries. Our results demonstrate that EvolSTAR is highly accurate and has a much improved call rate. The high throughput and short turn-around time from sample to sequence and analysis results (30 h for 24 samples) makes this kit an efficient largescale evolutionary biosurveillance tool. © The Author(s) 2010.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1093/nar/gkq089
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCOMPUTER SCIENCE
dc.description.doi10.1093/nar/gkq089
dc.description.sourcetitleNucleic Acids Research
dc.description.volume38
dc.description.issue9
dc.description.pagee111-e111
dc.description.codenNARHA
dc.identifier.isiut000277994600008
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