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Using false discovery rates to benchmark SNP-callers in next-generation sequencing projects

dc.contributor.authorFarrer, Rhys A
dc.contributor.authorHenk, Daniel A
dc.contributor.authorMacLean, Dan
dc.contributor.authorStudholme, David J
dc.contributor.authorFisher, Matthew C
dc.contributor.institutionUniversity of Aberdeen.Medical Sciencesen
dc.date.accessioned2018-11-02T16:20:05Z
dc.date.available2018-11-02T16:20:05Z
dc.date.issued2013-03-21
dc.descriptionFunding: R.A.F. was funded by the Natural Environment Research Council (NERC). D.A.H. and M.C.F. were supported by the Wellcome Trust. No additional external funding received for this study.en
dc.description.statusPeer revieweden
dc.format.extent6
dc.format.extent683237
dc.identifier140311338
dc.identifierf73ed354-685d-4478-a317-296bac8830f9
dc.identifier23518929
dc.identifier84875767941
dc.identifier.citationFarrer, R A, Henk, D A, MacLean, D, Studholme, D J & Fisher, M C 2013, 'Using false discovery rates to benchmark SNP-callers in next-generation sequencing projects', Scientific Reports, vol. 3, 1512. https://doi.org/10.1038/srep01512en
dc.identifier.doi10.1038/srep01512
dc.identifier.issn2045-2322
dc.identifier.otherPubMedCentral: PMC3604800
dc.identifier.otherORCID: /0000-0001-8456-7458/work/50284153
dc.identifier.urihttp://hdl.handle.net/2164/11384
dc.identifier.vol3en
dc.language.isoeng
dc.relation.ispartofScientific Reportsen
dc.subjectQH426 Geneticsen
dc.subjectNatural Environment Research Council (NERC)en
dc.subjectWellcome Trusten
dc.subject.lccQH426en
dc.titleUsing false discovery rates to benchmark SNP-callers in next-generation sequencing projectsen
dc.typeJournal articleen

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