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Statistical significance for hierarchical clustering in genetic association and microarray expression studies

BACKGROUND: With the increasing amount of data generated in molecular genetics laboratories, it is often difficult to make sense of results because of the vast number of different outcomes or variables studied. Examples include expression levels for large numbers of genes and haplotypes at large num...

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Autores principales: Levenstien, Mark A, Yang, Yaning, Ott, Jürg
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC328091/
https://www.ncbi.nlm.nih.gov/pubmed/14667254
http://dx.doi.org/10.1186/1471-2105-4-62
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author Levenstien, Mark A
Yang, Yaning
Ott, Jürg
author_facet Levenstien, Mark A
Yang, Yaning
Ott, Jürg
author_sort Levenstien, Mark A
collection PubMed
description BACKGROUND: With the increasing amount of data generated in molecular genetics laboratories, it is often difficult to make sense of results because of the vast number of different outcomes or variables studied. Examples include expression levels for large numbers of genes and haplotypes at large numbers of loci. It is then natural to group observations into smaller numbers of classes that allow for an easier overview and interpretation of the data. This grouping is often carried out in multiple steps with the aid of hierarchical cluster analysis, each step leading to a smaller number of classes by combining similar observations or classes. At each step, either implicitly or explicitly, researchers tend to interpret results and eventually focus on that set of classes providing the "best" (most significant) result. While this approach makes sense, the overall statistical significance of the experiment must include the clustering process, which modifies the grouping structure of the data and often removes variation. RESULTS: For hierarchically clustered data, we propose considering the strongest result or, equivalently, the smallest p-value as the experiment-wise statistic of interest and evaluating its significance level for a global assessment of statistical significance. We apply our approach to datasets from haplotype association and microarray expression studies where hierarchical clustering has been used. CONCLUSION: In all of the cases we examine, we find that relying on one set of classes in the course of clustering leads to significance levels that are too small when compared with the significance level associated with an overall statistic that incorporates the process of clustering. In other words, relying on one step of clustering may furnish a formally significant result while the overall experiment is not significant.
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spelling pubmed-3280912004-02-05 Statistical significance for hierarchical clustering in genetic association and microarray expression studies Levenstien, Mark A Yang, Yaning Ott, Jürg BMC Bioinformatics Methodology Article BACKGROUND: With the increasing amount of data generated in molecular genetics laboratories, it is often difficult to make sense of results because of the vast number of different outcomes or variables studied. Examples include expression levels for large numbers of genes and haplotypes at large numbers of loci. It is then natural to group observations into smaller numbers of classes that allow for an easier overview and interpretation of the data. This grouping is often carried out in multiple steps with the aid of hierarchical cluster analysis, each step leading to a smaller number of classes by combining similar observations or classes. At each step, either implicitly or explicitly, researchers tend to interpret results and eventually focus on that set of classes providing the "best" (most significant) result. While this approach makes sense, the overall statistical significance of the experiment must include the clustering process, which modifies the grouping structure of the data and often removes variation. RESULTS: For hierarchically clustered data, we propose considering the strongest result or, equivalently, the smallest p-value as the experiment-wise statistic of interest and evaluating its significance level for a global assessment of statistical significance. We apply our approach to datasets from haplotype association and microarray expression studies where hierarchical clustering has been used. CONCLUSION: In all of the cases we examine, we find that relying on one set of classes in the course of clustering leads to significance levels that are too small when compared with the significance level associated with an overall statistic that incorporates the process of clustering. In other words, relying on one step of clustering may furnish a formally significant result while the overall experiment is not significant. BioMed Central 2003-12-11 /pmc/articles/PMC328091/ /pubmed/14667254 http://dx.doi.org/10.1186/1471-2105-4-62 Text en Copyright © 2003 Levenstien et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Methodology Article
Levenstien, Mark A
Yang, Yaning
Ott, Jürg
Statistical significance for hierarchical clustering in genetic association and microarray expression studies
title Statistical significance for hierarchical clustering in genetic association and microarray expression studies
title_full Statistical significance for hierarchical clustering in genetic association and microarray expression studies
title_fullStr Statistical significance for hierarchical clustering in genetic association and microarray expression studies
title_full_unstemmed Statistical significance for hierarchical clustering in genetic association and microarray expression studies
title_short Statistical significance for hierarchical clustering in genetic association and microarray expression studies
title_sort statistical significance for hierarchical clustering in genetic association and microarray expression studies
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC328091/
https://www.ncbi.nlm.nih.gov/pubmed/14667254
http://dx.doi.org/10.1186/1471-2105-4-62
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