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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.date.accessioned2018-11-02T16:20:05Z
dc.date.available2018-11-02T16:20:05Z
dc.date.issued2013-03-21
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 . DOI: 10.1038/srep01512en
dc.identifier.issn2045-2322
dc.identifier.otherPURE: 140311338
dc.identifier.otherPURE UUID: f73ed354-685d-4478-a317-296bac8830f9
dc.identifier.otherPubMed: 23518929
dc.identifier.otherPubMedCentral: PMC3604800
dc.identifier.otherScopus: 84875767941
dc.identifier.urihttp://hdl.handle.net/2164/11384
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.format.extent6en
dc.language.isoeng
dc.relation.ispartofScientific Reportsen
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/en
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
dc.contributor.institutionUniversity of Aberdeen, Medical Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1038/srep01512


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