A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity
ABSTRACT Recent research has revealed loci that display variance heterogeneity through various means such as biological disruption, linkage disequilibrium (LD), gene‐by‐gene (G × G), or gene‐by‐environment interaction. We propose a versatile likelihood ratio test that allows joint testing for mean a...
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Veröffentlicht in: | Genetic epidemiology 2014-01, Vol.38 (1), p.51-59 |
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creator | Cao, Ying Wei, Peng Bailey, Matthew Kauwe, John S. K. Maxwell, Taylor J. |
description | ABSTRACT
Recent research has revealed loci that display variance heterogeneity through various means such as biological disruption, linkage disequilibrium (LD), gene‐by‐gene (G × G), or gene‐by‐environment interaction. We propose a versatile likelihood ratio test that allows joint testing for mean and variance heterogeneity (LRTMV) or either effect alone (LRTM or LRTV) in the presence of covariates. Using extensive simulations for our method and others, we found that all parametric tests were sensitive to nonnormality regardless of any trait transformations. Coupling our test with the parametric bootstrap solves this issue. Using simulations and empirical data from a known mean‐only functional variant, we demonstrate how LD can produce variance‐heterogeneity loci (vQTL) in a predictable fashion based on differential allele frequencies, high D′, and relatively low r2 values. We propose that a joint test for mean and variance heterogeneity is more powerful than a variance‐only test for detecting vQTL. This takes advantage of loci that also have mean effects without sacrificing much power to detect variance only effects. We discuss using vQTL as an approach to detect G × G interactions and also how vQTL are related to relationship loci, and how both can create prior hypothesis for each other and reveal the relationships between traits and possibly between components of a composite trait. |
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Recent research has revealed loci that display variance heterogeneity through various means such as biological disruption, linkage disequilibrium (LD), gene‐by‐gene (G × G), or gene‐by‐environment interaction. We propose a versatile likelihood ratio test that allows joint testing for mean and variance heterogeneity (LRTMV) or either effect alone (LRTM or LRTV) in the presence of covariates. Using extensive simulations for our method and others, we found that all parametric tests were sensitive to nonnormality regardless of any trait transformations. Coupling our test with the parametric bootstrap solves this issue. Using simulations and empirical data from a known mean‐only functional variant, we demonstrate how LD can produce variance‐heterogeneity loci (vQTL) in a predictable fashion based on differential allele frequencies, high D′, and relatively low r2 values. We propose that a joint test for mean and variance heterogeneity is more powerful than a variance‐only test for detecting vQTL. This takes advantage of loci that also have mean effects without sacrificing much power to detect variance only effects. We discuss using vQTL as an approach to detect G × G interactions and also how vQTL are related to relationship loci, and how both can create prior hypothesis for each other and reveal the relationships between traits and possibly between components of a composite trait.</description><identifier>ISSN: 0741-0395</identifier><identifier>EISSN: 1098-2272</identifier><identifier>DOI: 10.1002/gepi.21778</identifier><identifier>PMID: 24482837</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Alzheimer Disease - genetics ; G × E ; G × G ; Gene Frequency - genetics ; Genes ; Genotype ; GWAS ; Humans ; Likelihood Functions ; linkage disequilibrium ; Linkage Disequilibrium - genetics ; Matrix Metalloproteinase 3 - cerebrospinal fluid ; Matrix Metalloproteinase 3 - genetics ; Models, Genetic ; Phenotype ; Quantitative Trait Loci - genetics ; Research Design ; rQTL ; vQTL</subject><ispartof>Genetic epidemiology, 2014-01, Vol.38 (1), p.51-59</ispartof><rights>2013 WILEY PERIODICALS, INC.</rights><rights>2014 WILEY PERIODICALS, INC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5198-e73f22ff746b17d781658d5859536720c28ba837fa0450ad1883e274aa0d84f13</citedby><cites>FETCH-LOGICAL-c5198-e73f22ff746b17d781658d5859536720c28ba837fa0450ad1883e274aa0d84f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fgepi.21778$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fgepi.21778$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,777,781,882,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24482837$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Ying</creatorcontrib><creatorcontrib>Wei, Peng</creatorcontrib><creatorcontrib>Bailey, Matthew</creatorcontrib><creatorcontrib>Kauwe, John S. K.</creatorcontrib><creatorcontrib>Maxwell, Taylor J.</creatorcontrib><title>A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity</title><title>Genetic epidemiology</title><addtitle>Genet. Epidemiol</addtitle><description>ABSTRACT
Recent research has revealed loci that display variance heterogeneity through various means such as biological disruption, linkage disequilibrium (LD), gene‐by‐gene (G × G), or gene‐by‐environment interaction. We propose a versatile likelihood ratio test that allows joint testing for mean and variance heterogeneity (LRTMV) or either effect alone (LRTM or LRTV) in the presence of covariates. Using extensive simulations for our method and others, we found that all parametric tests were sensitive to nonnormality regardless of any trait transformations. Coupling our test with the parametric bootstrap solves this issue. Using simulations and empirical data from a known mean‐only functional variant, we demonstrate how LD can produce variance‐heterogeneity loci (vQTL) in a predictable fashion based on differential allele frequencies, high D′, and relatively low r2 values. We propose that a joint test for mean and variance heterogeneity is more powerful than a variance‐only test for detecting vQTL. This takes advantage of loci that also have mean effects without sacrificing much power to detect variance only effects. We discuss using vQTL as an approach to detect G × G interactions and also how vQTL are related to relationship loci, and how both can create prior hypothesis for each other and reveal the relationships between traits and possibly between components of a composite trait.</description><subject>Alzheimer Disease - genetics</subject><subject>G × E</subject><subject>G × G</subject><subject>Gene Frequency - genetics</subject><subject>Genes</subject><subject>Genotype</subject><subject>GWAS</subject><subject>Humans</subject><subject>Likelihood Functions</subject><subject>linkage disequilibrium</subject><subject>Linkage Disequilibrium - genetics</subject><subject>Matrix Metalloproteinase 3 - cerebrospinal fluid</subject><subject>Matrix Metalloproteinase 3 - genetics</subject><subject>Models, Genetic</subject><subject>Phenotype</subject><subject>Quantitative Trait Loci - genetics</subject><subject>Research Design</subject><subject>rQTL</subject><subject>vQTL</subject><issn>0741-0395</issn><issn>1098-2272</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1vEzEQxS0EoqFw4Q9AlrggpC0ef6y9F6SqH0mlQitUCuJiObuzwWXjDfYukP8eh7QRcIDTHOY3T-_NI-QpsANgjL9a4MofcNDa3CMTYJUpONf8PpkwLaFgolJ75FFKN4wByEo9JHtcSsON0BNyekivMSY3-A7pxTL4-ZjoFaaBtn2kxzhgPfiwoG_QBepCQ69d9C7USGd5F_sFBvTD-jF50Lou4ZPbuU_en55cHc2K84vp2dHheVEryL5Qi5bzttWynINutIFSmUYZVSlRas5qbuYu-2odk4q5BowRyLV0jjVGtiD2yeut7mqcL7GpMQzRdXYV_dLFte2dt39ugv9sF_03KxlUksks8OJWIPZfx5zTLn2qsetcwH5MFhSvKilLWf4flZUwbPPRjD7_C73pxxjyJzaCXKucXmfq5ZaqY59SxHbnG5jdNGk3TdpfTWb42e9Jd-hddRmALfA9V7f-h5Sdnlye3YkW2xufBvyxu3Hxiy210Mp-eDu1x58u2ezjO7BC_ATN3bYR</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Cao, Ying</creator><creator>Wei, Peng</creator><creator>Bailey, Matthew</creator><creator>Kauwe, John S. K.</creator><creator>Maxwell, Taylor J.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201401</creationdate><title>A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity</title><author>Cao, Ying ; Wei, Peng ; Bailey, Matthew ; Kauwe, John S. K. ; Maxwell, Taylor J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5198-e73f22ff746b17d781658d5859536720c28ba837fa0450ad1883e274aa0d84f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Alzheimer Disease - genetics</topic><topic>G × E</topic><topic>G × G</topic><topic>Gene Frequency - genetics</topic><topic>Genes</topic><topic>Genotype</topic><topic>GWAS</topic><topic>Humans</topic><topic>Likelihood Functions</topic><topic>linkage disequilibrium</topic><topic>Linkage Disequilibrium - genetics</topic><topic>Matrix Metalloproteinase 3 - cerebrospinal fluid</topic><topic>Matrix Metalloproteinase 3 - genetics</topic><topic>Models, Genetic</topic><topic>Phenotype</topic><topic>Quantitative Trait Loci - genetics</topic><topic>Research Design</topic><topic>rQTL</topic><topic>vQTL</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Ying</creatorcontrib><creatorcontrib>Wei, Peng</creatorcontrib><creatorcontrib>Bailey, Matthew</creatorcontrib><creatorcontrib>Kauwe, John S. K.</creatorcontrib><creatorcontrib>Maxwell, Taylor J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetic epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Ying</au><au>Wei, Peng</au><au>Bailey, Matthew</au><au>Kauwe, John S. K.</au><au>Maxwell, Taylor J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity</atitle><jtitle>Genetic epidemiology</jtitle><addtitle>Genet. Epidemiol</addtitle><date>2014-01</date><risdate>2014</risdate><volume>38</volume><issue>1</issue><spage>51</spage><epage>59</epage><pages>51-59</pages><issn>0741-0395</issn><eissn>1098-2272</eissn><abstract>ABSTRACT
Recent research has revealed loci that display variance heterogeneity through various means such as biological disruption, linkage disequilibrium (LD), gene‐by‐gene (G × G), or gene‐by‐environment interaction. We propose a versatile likelihood ratio test that allows joint testing for mean and variance heterogeneity (LRTMV) or either effect alone (LRTM or LRTV) in the presence of covariates. Using extensive simulations for our method and others, we found that all parametric tests were sensitive to nonnormality regardless of any trait transformations. Coupling our test with the parametric bootstrap solves this issue. Using simulations and empirical data from a known mean‐only functional variant, we demonstrate how LD can produce variance‐heterogeneity loci (vQTL) in a predictable fashion based on differential allele frequencies, high D′, and relatively low r2 values. We propose that a joint test for mean and variance heterogeneity is more powerful than a variance‐only test for detecting vQTL. This takes advantage of loci that also have mean effects without sacrificing much power to detect variance only effects. We discuss using vQTL as an approach to detect G × G interactions and also how vQTL are related to relationship loci, and how both can create prior hypothesis for each other and reveal the relationships between traits and possibly between components of a composite trait.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24482837</pmid><doi>10.1002/gepi.21778</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - genetics G × E G × G Gene Frequency - genetics Genes Genotype GWAS Humans Likelihood Functions linkage disequilibrium Linkage Disequilibrium - genetics Matrix Metalloproteinase 3 - cerebrospinal fluid Matrix Metalloproteinase 3 - genetics Models, Genetic Phenotype Quantitative Trait Loci - genetics Research Design rQTL vQTL |
title | A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity |
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