Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1837
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dc.contributor.authorJanies, Daniel A.en_US
dc.contributor.authorTreseder, Travisen_US
dc.contributor.authorAlexandrov, Boyanen_US
dc.contributor.authorHABIB, FARHATen_US
dc.contributor.authorChen, Jennifer J.en_US
dc.contributor.authorFerreira, Renatoen_US
dc.contributor.authorCatalyurek, Umiten_US
dc.contributor.authorVaron, Andresen_US
dc.contributor.authorWheeler, Ward C.en_US
dc.date.accessioned2019-02-14T05:52:32Z
dc.date.available2019-02-14T05:52:32Z
dc.date.issued2011-01en_US
dc.identifier.citationCladistics, 27(1), 61-66.en_US
dc.identifier.issn0748-3007en_US
dc.identifier.issn1096-0031en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1837-
dc.identifier.urihttps://doi.org/10.1111/j.1096-0031.2010.00314.xen_US
dc.description.abstractNovel pathogens have the potential to become critical issues of national security, public health and economic welfare. As demonstrated by the response to Severe Acute Respiratory Syndrome (SARS) and influenza, genomic sequencing has become an important method for diagnosing agents of infectious disease. Despite the value of genomic sequences in characterizing novel pathogens, raw data on their own do not provide the information needed by public health officials and researchers. One must integrate knowledge of the genomes of pathogens with host biology and geography to understand the etiology of epidemics. To these ends, we have created an application called Supramap (http://supramap.osu.edu) to put information on the spread of pathogens and key mutations across time, space and various hosts into a geographic information system (GIS). To build this application, we created a web service for integrated sequence alignment and phylogenetic analysis as well as methods to describe the tree, mutations, and host shifts in Keyhole Markup Language (KML). We apply the application to 239 sequences of the polymerase basic 2 (PB2) gene of recent isolates of avian influenza (H5N1). We map a mutation, glutamic acid to lysine at position 627 in the PB2 protein (E627K), in H5N1 influenza that allows for increased replication of the virus in mammals. We use a statistical test to support the hypothesis of a correlation of E627K mutations with avian?mammalian host shifts but reject the hypothesis that lineages with E627K are moving westward. Data, instructions for use, and visualizations are included as supplemental materials.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectSupramap Projecten_US
dc.subjectInfectious diseasesen_US
dc.subjectNovel pathogensen_US
dc.subjectComputing poweren_US
dc.subjectPathogen genomic dataen_US
dc.subjectPhylogenetic analysesen_US
dc.subject2011en_US
dc.titleThe Supramap project: linking pathogen genomes with geography to fight emergent infectious diseasesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleCladisticsen_US
dc.publication.originofpublisherForeignen_US
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