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Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis

We examined the properties of growth mixture modeling in finding longitudinal quantitative trait loci in a genome-wide association study. Two software packages are commonly used in these analyses: Mplus and the SAS TRAJ procedure. We analyzed the 200 replicates of the simulated data with these progr...

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Autores principales: Chang, Su-Wei, Choi, Seung Hoan, Li, Ke, Fleur, Rose Saint, Huang, Chengrui, Shen, Tong, Ahn, Kwangmi, Gordon, Derek, Kim, Wonkuk, Wu, Rongling, Mendell, Nancy R, Finch, Stephen J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795884/
https://www.ncbi.nlm.nih.gov/pubmed/20017977
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author Chang, Su-Wei
Choi, Seung Hoan
Li, Ke
Fleur, Rose Saint
Huang, Chengrui
Shen, Tong
Ahn, Kwangmi
Gordon, Derek
Kim, Wonkuk
Wu, Rongling
Mendell, Nancy R
Finch, Stephen J
author_facet Chang, Su-Wei
Choi, Seung Hoan
Li, Ke
Fleur, Rose Saint
Huang, Chengrui
Shen, Tong
Ahn, Kwangmi
Gordon, Derek
Kim, Wonkuk
Wu, Rongling
Mendell, Nancy R
Finch, Stephen J
author_sort Chang, Su-Wei
collection PubMed
description We examined the properties of growth mixture modeling in finding longitudinal quantitative trait loci in a genome-wide association study. Two software packages are commonly used in these analyses: Mplus and the SAS TRAJ procedure. We analyzed the 200 replicates of the simulated data with these programs using three tests: the likelihood-ratio test statistic, a direct test of genetic model coefficients, and the chi-square test classifying subjects based on the trajectory model's posterior Bayesian probability. The Mplus program was not effective in this application due to its computational demands. The distributions of these tests applied to genes not related to the trait were sensitive to departures from Hardy-Weinberg equilibrium. The likelihood-ratio test statistic was not usable in this application because its distribution was far from the expected asymptotic distributions when applied to markers with no genetic relation to the quantitative trait. The other two tests were satisfactory. Power was still substantial when we used markers near the gene rather than the gene itself. That is, growth mixture modeling may be useful in genome-wide association studies. For markers near the actual gene, there was somewhat greater power for the direct test of the coefficients and lesser power for the posterior Bayesian probability chi-square test.
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spelling pubmed-27958842009-12-18 Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis Chang, Su-Wei Choi, Seung Hoan Li, Ke Fleur, Rose Saint Huang, Chengrui Shen, Tong Ahn, Kwangmi Gordon, Derek Kim, Wonkuk Wu, Rongling Mendell, Nancy R Finch, Stephen J BMC Proc Proceedings We examined the properties of growth mixture modeling in finding longitudinal quantitative trait loci in a genome-wide association study. Two software packages are commonly used in these analyses: Mplus and the SAS TRAJ procedure. We analyzed the 200 replicates of the simulated data with these programs using three tests: the likelihood-ratio test statistic, a direct test of genetic model coefficients, and the chi-square test classifying subjects based on the trajectory model's posterior Bayesian probability. The Mplus program was not effective in this application due to its computational demands. The distributions of these tests applied to genes not related to the trait were sensitive to departures from Hardy-Weinberg equilibrium. The likelihood-ratio test statistic was not usable in this application because its distribution was far from the expected asymptotic distributions when applied to markers with no genetic relation to the quantitative trait. The other two tests were satisfactory. Power was still substantial when we used markers near the gene rather than the gene itself. That is, growth mixture modeling may be useful in genome-wide association studies. For markers near the actual gene, there was somewhat greater power for the direct test of the coefficients and lesser power for the posterior Bayesian probability chi-square test. BioMed Central 2009-12-15 /pmc/articles/PMC2795884/ /pubmed/20017977 Text en Copyright ©2009 Chang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Chang, Su-Wei
Choi, Seung Hoan
Li, Ke
Fleur, Rose Saint
Huang, Chengrui
Shen, Tong
Ahn, Kwangmi
Gordon, Derek
Kim, Wonkuk
Wu, Rongling
Mendell, Nancy R
Finch, Stephen J
Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
title Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
title_full Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
title_fullStr Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
title_full_unstemmed Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
title_short Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
title_sort growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795884/
https://www.ncbi.nlm.nih.gov/pubmed/20017977
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