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Comparison of biometrical models for joint linkage association mapping
Joint linkage association mapping (JLAM) combines the advantages of linkage mapping and association mapping, and is a powerful tool to dissect the genetic architecture of complex traits. The main goal of this study was to use a cross-validation strategy, resample model averaging and empirical data a...
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Published in: | Heredity 2012-03, Vol.108 (3), p.332-340 |
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description | Joint linkage association mapping (JLAM) combines the advantages of linkage mapping and association mapping, and is a powerful tool to dissect the genetic architecture of complex traits. The main goal of this study was to use a cross-validation strategy, resample model averaging and empirical data analyses to compare seven different biometrical models for JLAM with regard to the correction for population structure and the quantitative trait loci (QTL) detection power. Three linear models and four linear mixed models with different approaches to control for population stratification were evaluated. Models A, B and C were linear models with either cofactors (Model-A), or cofactors and a population effect (Model-B), or a model in which the cofactors and the single-nucleotide polymorphism effect were modeled as nested within population (Model-C). The mixed models, D, E, F and G, included a random population effect (Model-D), or a random population effect with defined variance structure (Model-E), a kinship matrix defining the degree of relatedness among the genotypes (Model-F), or a kinship matrix and principal coordinates (Model-G). The tested models were conceptually different and were also found to differ in terms of power to detect QTL. Model-B with the cofactors and a population effect, effectively controlled population structure and possessed a high predictive power. The varying allele substitution effects in different populations suggest as a promising strategy for JLAM to use Model-B for the detection of QTL and then to estimate their effects by applying Model-C. |
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The tested models were conceptually different and were also found to differ in terms of power to detect QTL. Model-B with the cofactors and a population effect, effectively controlled population structure and possessed a high predictive power. The varying allele substitution effects in different populations suggest as a promising strategy for JLAM to use Model-B for the detection of QTL and then to estimate their effects by applying Model-C.</description><identifier>ISSN: 0018-067X</identifier><identifier>EISSN: 1365-2540</identifier><identifier>DOI: 10.1038/hdy.2011.78</identifier><identifier>PMID: 21878984</identifier><identifier>CODEN: HDTYAT</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Beta vulgaris - genetics ; Biomedical and Life Sciences ; Biomedicine ; Biometrics ; Chromosome Mapping ; Comparative studies ; Cytogenetics ; Ecology ; Evolutionary Biology ; Gene mapping ; Genetic Linkage ; Genotype ; Genotypes ; Human Genetics ; Linkage Disequilibrium ; Models, Genetic ; Models, Statistical ; Original ; original-article ; Plant Genetics and Genomics ; Population structure ; Quantitative Trait Loci ; Reproducibility of Results</subject><ispartof>Heredity, 2012-03, Vol.108 (3), p.332-340</ispartof><rights>The Genetics Society 2012</rights><rights>Copyright Nature Publishing Group Mar 2012</rights><rights>Copyright © 2012 The Genetics Society 2012 The Genetics Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-83c2df075bc5309662cd9d5c71fc4218bae4eaef6a4d7c364e7386a6e63d124c3</citedby><cites>FETCH-LOGICAL-c476t-83c2df075bc5309662cd9d5c71fc4218bae4eaef6a4d7c364e7386a6e63d124c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282402/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282402/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21878984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Würschum, T</creatorcontrib><creatorcontrib>Liu, W</creatorcontrib><creatorcontrib>Gowda, M</creatorcontrib><creatorcontrib>Maurer, H P</creatorcontrib><creatorcontrib>Fischer, S</creatorcontrib><creatorcontrib>Schechert, A</creatorcontrib><creatorcontrib>Reif, J C</creatorcontrib><title>Comparison of biometrical models for joint linkage association mapping</title><title>Heredity</title><addtitle>Heredity</addtitle><addtitle>Heredity (Edinb)</addtitle><description>Joint linkage association mapping (JLAM) combines the advantages of linkage mapping and association mapping, and is a powerful tool to dissect the genetic architecture of complex traits. 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The tested models were conceptually different and were also found to differ in terms of power to detect QTL. Model-B with the cofactors and a population effect, effectively controlled population structure and possessed a high predictive power. 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subjects | Beta vulgaris - genetics Biomedical and Life Sciences Biomedicine Biometrics Chromosome Mapping Comparative studies Cytogenetics Ecology Evolutionary Biology Gene mapping Genetic Linkage Genotype Genotypes Human Genetics Linkage Disequilibrium Models, Genetic Models, Statistical Original original-article Plant Genetics and Genomics Population structure Quantitative Trait Loci Reproducibility of Results |
title | Comparison of biometrical models for joint linkage association mapping |
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