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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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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. |
format | Text |
id | pubmed-2795884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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