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Extended pedigree patterned covariance matrix mixed models for quantitative phenotype analysis

dc.contributor.authorSchork, Nicholas J.en_US
dc.date.accessioned2006-04-28T17:01:20Z
dc.date.available2006-04-28T17:01:20Z
dc.date.issued1992en_US
dc.identifier.citationSchork, Nicholas J. (1992)."Extended pedigree patterned covariance matrix mixed models for quantitative phenotype analysis." Genetic Epidemiology 9(2): 73-86. <http://hdl.handle.net/2027.42/38501>en_US
dc.identifier.issn0741-0395en_US
dc.identifier.issn1098-2272en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38501
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1639246&dopt=citationen_US
dc.description.abstractOvert computational constraints in the formation of mixed models for the analysis of large extended-pedigree quantitative trait data which allow one to reliably characterize and partition sources of variation resulting from a variety sources have proven difficult to overcome. The present paper suggests that by combining a restricted patterned covariance matrix approach to modeling and partitioning the variation arising from polygenic and environmental forces with an Elston–Stewart like algorithmic approach to modeling variation resulting from a single genetic locus with large phenotypic effects one can produce a model that is at once intuitively appealing, efficient computationally, and reliable numerically. Extensions and variations of this approach are also discussed, as are some simulation and timing studies carried out in an effort to validate the accuracy and computational efficiency of the proposed methodology. © 1992 Wiley-Liss, Inc.en_US
dc.format.extent855419 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleExtended pedigree patterned covariance matrix mixed models for quantitative phenotype analysisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Hypertension, Department of Medicine and Department of Epidemiology, University of Michigan, Ann Arbor, Michigan ; Department of Medicine and Department of Epidemiology, University of Michigan, R6592 Kresge I, Ann Arbor, MI 48109-0500en_US
dc.identifier.pmid1639246en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38501/1/1370090202_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/gepi.1370090202en_US
dc.identifier.sourceGenetic Epidemiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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