Validating, augmenting and refining genome-wide association signals

dc.contributor.authorIoannidis, J. P.en
dc.contributor.authorThomas, G.en
dc.contributor.authorDaly, M. J.en
dc.date.accessioned2015-11-24T18:53:24Z
dc.date.available2015-11-24T18:53:24Z
dc.identifier.issn1471-0064-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18554
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectGenetic Heterogeneityen
dc.subjectGenetic Linkageen
dc.subjectGenomeen
dc.subjectGenome-Wide Association Study/*methodsen
dc.subjectHumansen
dc.subjectPhenotypeen
dc.subjectReproducibility of Resultsen
dc.titleValidating, augmenting and refining genome-wide association signalsen
heal.abstractStudies using genome-wide platforms have yielded an unprecedented number of promising signals of association between genomic variants and human traits. This Review addresses the steps required to validate, augment and refine such signals to identify underlying causal variants for well-defined phenotypes. These steps include: large-scale exact replication across both similar and diverse populations; fine mapping and resequencing; determination of the most informative markers and multiple independent informative loci; incorporation of functional information; and improved phenotype mapping of the implicated genetic effects. Even in cases for which replication proves that an effect exists, confident localization of the causal variant often remains elusive.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1038/nrg2544-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/19373277-
heal.journalNameNat Rev Geneten
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2009-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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