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Adjusting for covariates on a slippery slope: linkage analysis of change over time

BACKGROUND: We analyzed the Genetic Analysis Workshop 13 (GAW13) simulated data to contrast and compare different methods for the genetic linkage analysis of hypertension and change in blood pressure over time. We also examined methods for incorporating covariates into the linkage analysis. We used...

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Autores principales: Rampersaud, Evadnie, Allen, Andrew, Li, Yi-Ju, Shao, Yujun, Bass, Meredyth, Haynes, Carol, Ashley-Koch, Allison, Martin, Eden R, Schmidt, Silke, Hauser, Elizabeth R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866487/
https://www.ncbi.nlm.nih.gov/pubmed/14975118
http://dx.doi.org/10.1186/1471-2156-4-S1-S50
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author Rampersaud, Evadnie
Allen, Andrew
Li, Yi-Ju
Shao, Yujun
Bass, Meredyth
Haynes, Carol
Ashley-Koch, Allison
Martin, Eden R
Schmidt, Silke
Hauser, Elizabeth R
author_facet Rampersaud, Evadnie
Allen, Andrew
Li, Yi-Ju
Shao, Yujun
Bass, Meredyth
Haynes, Carol
Ashley-Koch, Allison
Martin, Eden R
Schmidt, Silke
Hauser, Elizabeth R
author_sort Rampersaud, Evadnie
collection PubMed
description BACKGROUND: We analyzed the Genetic Analysis Workshop 13 (GAW13) simulated data to contrast and compare different methods for the genetic linkage analysis of hypertension and change in blood pressure over time. We also examined methods for incorporating covariates into the linkage analysis. We used methods for quantitative trait loci (QTL) linkage analysis with and without covariates and affected sib-pair (ASP) analysis of hypertension followed by ordered subset analysis (OSA), using variables associated with change in blood pressure over time. RESULTS: Four of the five baseline genes and one of the three slope genes were not detected by any method using conventional criteria. OSA detected baseline gene b35 on chromosome 13 when using the slope in blood pressure to adjust for change over time. Slope gene s10 was detected by the ASP analysis and slope gene s11 was detected by QTL linkage analysis as well as by OSA analysis. Analysis of null chromosomes, i.e., chromosomes without genes, did not reveal significant increases in type I error. However, there were a number of genes indirectly related to blood pressure detected by a variety of methods. CONCLUSIONS: We noted that there is no obvious first choice of analysis software for analyzing a complicated model, such as the one underlying the GAW13 simulated data. Inclusion of covariates and longitudinal data can improve localization of genes for complex traits but it is not always clear how best to do this. It remains a worthwhile task to apply several different approaches since one method is not always the best.
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spelling pubmed-18664872007-05-11 Adjusting for covariates on a slippery slope: linkage analysis of change over time Rampersaud, Evadnie Allen, Andrew Li, Yi-Ju Shao, Yujun Bass, Meredyth Haynes, Carol Ashley-Koch, Allison Martin, Eden R Schmidt, Silke Hauser, Elizabeth R BMC Genet Proceedings BACKGROUND: We analyzed the Genetic Analysis Workshop 13 (GAW13) simulated data to contrast and compare different methods for the genetic linkage analysis of hypertension and change in blood pressure over time. We also examined methods for incorporating covariates into the linkage analysis. We used methods for quantitative trait loci (QTL) linkage analysis with and without covariates and affected sib-pair (ASP) analysis of hypertension followed by ordered subset analysis (OSA), using variables associated with change in blood pressure over time. RESULTS: Four of the five baseline genes and one of the three slope genes were not detected by any method using conventional criteria. OSA detected baseline gene b35 on chromosome 13 when using the slope in blood pressure to adjust for change over time. Slope gene s10 was detected by the ASP analysis and slope gene s11 was detected by QTL linkage analysis as well as by OSA analysis. Analysis of null chromosomes, i.e., chromosomes without genes, did not reveal significant increases in type I error. However, there were a number of genes indirectly related to blood pressure detected by a variety of methods. CONCLUSIONS: We noted that there is no obvious first choice of analysis software for analyzing a complicated model, such as the one underlying the GAW13 simulated data. Inclusion of covariates and longitudinal data can improve localization of genes for complex traits but it is not always clear how best to do this. It remains a worthwhile task to apply several different approaches since one method is not always the best. BioMed Central 2003-12-31 /pmc/articles/PMC1866487/ /pubmed/14975118 http://dx.doi.org/10.1186/1471-2156-4-S1-S50 Text en Copyright © 2003 Rampersaud 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
Rampersaud, Evadnie
Allen, Andrew
Li, Yi-Ju
Shao, Yujun
Bass, Meredyth
Haynes, Carol
Ashley-Koch, Allison
Martin, Eden R
Schmidt, Silke
Hauser, Elizabeth R
Adjusting for covariates on a slippery slope: linkage analysis of change over time
title Adjusting for covariates on a slippery slope: linkage analysis of change over time
title_full Adjusting for covariates on a slippery slope: linkage analysis of change over time
title_fullStr Adjusting for covariates on a slippery slope: linkage analysis of change over time
title_full_unstemmed Adjusting for covariates on a slippery slope: linkage analysis of change over time
title_short Adjusting for covariates on a slippery slope: linkage analysis of change over time
title_sort adjusting for covariates on a slippery slope: linkage analysis of change over time
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866487/
https://www.ncbi.nlm.nih.gov/pubmed/14975118
http://dx.doi.org/10.1186/1471-2156-4-S1-S50
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