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dc.creatorDimou N.L., Tsirigos K.D., Elofsson A., Bagos P.G.en
dc.date.accessioned2023-01-31T07:56:49Z
dc.date.available2023-01-31T07:56:49Z
dc.date.issued2017
dc.identifier10.1093/bioinformatics/btx008
dc.identifier.issn13674803
dc.identifier.urihttp://hdl.handle.net/11615/73360
dc.description.abstractMotivation: In the context of genome-wide association studies (GWAS), there is a variety of statistical techniques in order to conduct the analysis, but, in most cases, the underlying genetic model is usually unknown. Under these circumstances, the classical Cochran-Armitage trend test (CATT) is suboptimal. Robust procedures that maximize the power and preserve the nominal type I error rate are preferable. Moreover, performing a meta-analysis using robust procedures is of great interest and has never been addressed in the past. The primary goal of this work is to implement several robust methods for analysis and meta-analysis in the statistical package Stata and subsequently to make the software available to the scientific community. Results: The CATT under a recessive, additive and dominant model of inheritance as well as robust methods based on the Maximum Efficiency Robust Test statistic, the MAX statistic and the MIN2 were implemented in Stata. Concerning MAX and MIN2, we calculated their asymptotic null distributions relying on numerical integration resulting in a great gain in computational time without losing accuracy. All the aforementioned approaches were employed in a fixed or a random effects meta-analysis setting using summary data with weights equal to the reciprocal of the combined cases and controls. Overall, this is the first complete effort to implement procedures for analysis and meta-analysis in GWAS using Stata. Availability and Implementation: A Stata program and a web-server are freely available for academic users at http://www.compgen.org/tools/GWAR . © The Author 2017.en
dc.language.isoenen
dc.sourceBioinformaticsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85020279446&doi=10.1093%2fbioinformatics%2fbtx008&partnerID=40&md5=069c9a1b625becdf74b11fc3bb8ffc30
dc.subjectbiological modelen
dc.subjectgenetic predispositionen
dc.subjectgeneticsen
dc.subjectgenome-wide association studyen
dc.subjectgenomicsen
dc.subjecthumanen
dc.subjecthypertensionen
dc.subjectmeta analysis (topic)en
dc.subjectpopulation geneticsen
dc.subjectproceduresen
dc.subjectsingle nucleotide polymorphismen
dc.subjectsoftwareen
dc.subjectstatisticsen
dc.subjectstatistics and numerical dataen
dc.subjectGenetic Predisposition to Diseaseen
dc.subjectGenetics, Populationen
dc.subjectGenome-Wide Association Studyen
dc.subjectGenomicsen
dc.subjectHumansen
dc.subjectHypertensionen
dc.subjectMeta-Analysis as Topicen
dc.subjectModels, Geneticen
dc.subjectPolymorphism, Single Nucleotideen
dc.subjectSoftwareen
dc.subjectStatistics as Topicen
dc.subjectOxford University Pressen
dc.titleGWAR: Robust analysis and meta-analysis of genome-wide association studiesen
dc.typejournalArticleen


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