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

Farrer, Rhys AHenk, Daniel AMacLean, DanStudholme, David JFisher, Matthew C2018-11-022018-11-022013-03-21Farrer, 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/srep015122045-2322PubMedCentral: PMC3604800ORCID: /0000-0001-8456-7458/work/50284153http://hdl.handle.net/2164/11384Funding: 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.6683237engQH426 GeneticsNatural Environment Research Council (NERC)Wellcome TrustQH426Using false discovery rates to benchmark SNP-callers in next-generation sequencing projectsJournal article10.1038/srep015123