Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data

<p>Abstract</p> <p>Background</p> <p>The causes of complex diseases are difficult to grasp since many different factors play a role in their onset. To find a common genetic background, many of the existing studies divide their population into controls and cases; a class...

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Main Authors: Zwinderman Aeilko H, Waaijenborg Sandra
Format: Article
Language:English
Published: BMC 2010-02-01
Series:Algorithms for Molecular Biology
Online Access:http://www.almob.org/content/5/1/17
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spelling doaj-8e986c2a61814a0ba5a824cd15236cab2020-11-24T21:21:30ZengBMCAlgorithms for Molecular Biology1748-71882010-02-01511710.1186/1748-7188-5-17Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP dataZwinderman Aeilko HWaaijenborg Sandra<p>Abstract</p> <p>Background</p> <p>The causes of complex diseases are difficult to grasp since many different factors play a role in their onset. To find a common genetic background, many of the existing studies divide their population into controls and cases; a classification that is likely to cause heterogeneity within the two groups. Rather than dividing the study population into cases and controls, it is better to identify the phenotype of a complex disease by a set of intermediate risk factors. But these risk factors often vary over time and are therefore repeatedly measured.</p> <p>Results</p> <p>We introduce a method to associate multiple repeatedly measured intermediate risk factors with a high dimensional set of single nucleotide polymorphisms (SNPs). Via a two-step approach, we summarized the time courses of each individual and, secondly apply these to penalized nonlinear canonical correlation analysis to obtain sparse results.</p> <p>Conclusions</p> <p>Application of this method to two datasets which study the genetic background of cardiovascular diseases, show that compared to progression over time, mainly the constant levels in time are associated with sets of SNPs.</p> http://www.almob.org/content/5/1/17
collection DOAJ
language English
format Article
sources DOAJ
author Zwinderman Aeilko H
Waaijenborg Sandra
spellingShingle Zwinderman Aeilko H
Waaijenborg Sandra
Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data
Algorithms for Molecular Biology
author_facet Zwinderman Aeilko H
Waaijenborg Sandra
author_sort Zwinderman Aeilko H
title Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data
title_short Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data
title_full Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data
title_fullStr Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data
title_full_unstemmed Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data
title_sort association of repeatedly measured intermediate risk factors for complex diseases with high dimensional snp data
publisher BMC
series Algorithms for Molecular Biology
issn 1748-7188
publishDate 2010-02-01
description <p>Abstract</p> <p>Background</p> <p>The causes of complex diseases are difficult to grasp since many different factors play a role in their onset. To find a common genetic background, many of the existing studies divide their population into controls and cases; a classification that is likely to cause heterogeneity within the two groups. Rather than dividing the study population into cases and controls, it is better to identify the phenotype of a complex disease by a set of intermediate risk factors. But these risk factors often vary over time and are therefore repeatedly measured.</p> <p>Results</p> <p>We introduce a method to associate multiple repeatedly measured intermediate risk factors with a high dimensional set of single nucleotide polymorphisms (SNPs). Via a two-step approach, we summarized the time courses of each individual and, secondly apply these to penalized nonlinear canonical correlation analysis to obtain sparse results.</p> <p>Conclusions</p> <p>Application of this method to two datasets which study the genetic background of cardiovascular diseases, show that compared to progression over time, mainly the constant levels in time are associated with sets of SNPs.</p>
url http://www.almob.org/content/5/1/17
work_keys_str_mv AT zwindermanaeilkoh associationofrepeatedlymeasuredintermediateriskfactorsforcomplexdiseaseswithhighdimensionalsnpdata
AT waaijenborgsandra associationofrepeatedlymeasuredintermediateriskfactorsforcomplexdiseaseswithhighdimensionalsnpdata
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