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Lod scores for gene mapping in the presence of marker map uncertainty

dc.contributor.authorStringham, Heather M.en_US
dc.contributor.authorBoehnke, Michaelen_US
dc.date.accessioned2006-04-19T13:59:29Z
dc.date.available2006-04-19T13:59:29Z
dc.date.issued2001-07en_US
dc.identifier.citationStringham, Heather M.; Boehnke, Michael (2001)."Lod scores for gene mapping in the presence of marker map uncertainty." Genetic Epidemiology 21(1): 31-39. <http://hdl.handle.net/2027.42/34934>en_US
dc.identifier.issn0741-0395en_US
dc.identifier.issn1098-2272en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34934
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11443732&dopt=citationen_US
dc.description.abstractMultipoint lod scores are typically calculated for a grid of locus positions, moving the putative disease locus across a fixed map of genetic markers. Changing the order of a set of markers and/or the distances between the markers can make a substantial difference in the resulting lod score curve and the location and height of its maximum. The typical approach of using the best maximum likelihood marker map is not easily justified if other marker orders are nearly as likely and give substantially different lod score curves. To deal with this problem, we propose three weighted multipoint lod score statistics that make use of information from all plausible marker orders. In each of these statistics, the information conditional on a particular marker order is included in a weighted sum, with weight equal to the posterior probability of that order. We evaluate the type 1 error rate and power of these three statistics on the basis of results from simulated data, and compare these results to those obtained using the best maximum likelihood map and the map with the true marker order. We find that the lod score based on a weighted sum of maximum likelihoods improves on using only the best maximum likelihood map, having a type 1 error rate and power closest to that of using the true marker order in the simulation scenarios we considered. Genet. Epidemiol. 21:31–39, 2001. © 2001 Wiley-Liss, Inc.en_US
dc.format.extent51109 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleLod scores for gene mapping in the presence of marker map uncertaintyen_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.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arboren_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arbor ; Department of Biostatistics, School of Public Health, University of Michigan, 1420 Washington Heights, Ann Arbor, MI 48109-2029en_US
dc.identifier.pmid11443732en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34934/1/1016_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/gepi.1016en_US
dc.identifier.sourceGenetic Epidemiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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