Publication:
Comparison of Methods to Account for Relatedness in Genome-Wide Association Studies with Family-Based Data

dc.contributor.authorJakris Eu-ahsunthornwattanaen_US
dc.contributor.authorE. Nancy Milleren_US
dc.contributor.authorMichaela Fakiolaen_US
dc.contributor.authorSelma M.B. Jeronimoen_US
dc.contributor.authorJenefer M. Blackwellen_US
dc.contributor.authorHeather J. Cordellen_US
dc.contributor.otherNewcastle University, United Kingdomen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherCambridge Institute for Medical Researchen_US
dc.contributor.otherUniversidade Federal do Rio Grande do Norteen_US
dc.contributor.otherTelethon Kids Instituteen_US
dc.date.accessioned2018-11-09T01:48:37Z
dc.date.available2018-11-09T01:48:37Z
dc.date.issued2014-01-01en_US
dc.description.abstractApproaches based on linear mixed models (LMMs) have recently gained popularity for modelling population substructure and relatedness in genome-wide association studies. In the last few years, a bewildering variety of different LMM methods/software packages have been developed, but it is not always clear how (or indeed whether) any newly-proposed method differs from previously-proposed implementations. Here we compare the performance of several LMM approaches (and software implementations, including EMMAX, GenABEL, FaST-LMM, Mendel, GEMMA and MMM) via their application to a genome-wide association study of visceral leishmaniasis in 348 Brazilian families comprising 3626 individuals (1972 genotyped). The implementations differ in precise details of methodology implemented and through various user-chosen options such as the method and number of SNPs used to estimate the kinship (relatedness) matrix. We investigate sensitivity to these choices and the success (or otherwise) of the approaches in controlling the overall genome-wide error-rate for both real and simulated phenotypes. We compare the LMM results to those obtained using traditional family-based association tests (based on transmission of alleles within pedigrees) and to alternative approaches implemented in the software packages MQLS, ROADTRIPS and MASTOR. We find strong concordance between the results from different LMM approaches, and all are successful in controlling the genome-wide error rate (except for some approaches when applied naively to longitudinal data with many repeated measures). We also find high correlation between LMMs and alternative approaches (apart from transmission-based approaches when applied to SNPs with small or non-existent effects). We conclude that LMM approaches perform well in comparison to competing approaches. Given their strong concordance, in most applications, the choice of precise LMM implementation cannot be based on power/type I error considerations but must instead be based on considerations such as speed and ease-of-use. © 2014 Eu-ahsunthornwattana et al.en_US
dc.identifier.citationPLoS Genetics. Vol.10, No.7 (2014)en_US
dc.identifier.doi10.1371/journal.pgen.1004445en_US
dc.identifier.issn15537404en_US
dc.identifier.issn15537390en_US
dc.identifier.other2-s2.0-84905455421en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/33170
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84905455421&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleComparison of Methods to Account for Relatedness in Genome-Wide Association Studies with Family-Based Dataen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84905455421&origin=inwarden_US

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