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dc.contributor.authorWood, AR
dc.contributor.authorTuke, MA
dc.contributor.authorNalls, MA
dc.contributor.authorHernandez, DG
dc.contributor.authorBandinelli, S
dc.contributor.authorSingleton, AB
dc.contributor.authorMelzer, D
dc.contributor.authorFerrucci, L
dc.contributor.authorFrayling, TM
dc.contributor.authorWeedon, MN
dc.date.accessioned2017-03-13T08:57:07Z
dc.date.issued2014-10-02
dc.description.abstractEpistasis occurs when the effect of a genetic variant on a trait is dependent on genotypes of other variants elsewhere in the genome. Hemani et al. recently reported the detection and replication of many instances of epistasis between pairs of variants influencing gene expression levels in humans1. Using whole-genome sequencing data from 450 individuals we strongly replicated many of the reported interactions but, in each case, a single third variant captured by our sequencing data could explain all of the apparent epistasis. Our results provide an alternative explanation for the apparent epistasis observed for gene expression in humans. There is a Reply to this Brief Communication Arising by Hemani, G. et al. Nature 514, http://dx.doi.org/10.1038/nature13692 (2014).en_GB
dc.identifier.citationVol. 514, pp. E3 - E5en_GB
dc.identifier.doi10.1038/nature13691
dc.identifier.othernature13691
dc.identifier.urihttp://hdl.handle.net/10871/26475
dc.language.isoenen_GB
dc.publisherNature Publishing Groupen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/25279928en_GB
dc.subjectEpistasis, Geneticen_GB
dc.subjectFemaleen_GB
dc.subjectGene Expression Regulationen_GB
dc.subjectHumansen_GB
dc.subjectMaleen_GB
dc.subjectTranscription, Geneticen_GB
dc.titleAnother explanation for apparent epistasisen_GB
dc.typeArticleen_GB
dc.date.available2017-03-13T08:57:07Z
exeter.place-of-publicationEngland
dc.descriptionThis is the author accepted manuscript. The final version is available from the publisher via the DOI in this record.en_GB
dc.identifier.journalNatureen_GB
dc.identifier.pmid25279928


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