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Two-part permutation tests for DNA methylation and microarray data

BACKGROUND: One important application of microarray experiments is to identify differentially expressed genes. Often, small and negative expression levels were clipped-off to be equal to an arbitrarily chosen cutoff value before a statistical test is carried out. Then, there are two types of data: t...

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Autores principales: Neuhäuser, Markus, Boes, Tanja, Jöckel, Karl-Heinz
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC551601/
https://www.ncbi.nlm.nih.gov/pubmed/15725357
http://dx.doi.org/10.1186/1471-2105-6-35
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author Neuhäuser, Markus
Boes, Tanja
Jöckel, Karl-Heinz
author_facet Neuhäuser, Markus
Boes, Tanja
Jöckel, Karl-Heinz
author_sort Neuhäuser, Markus
collection PubMed
description BACKGROUND: One important application of microarray experiments is to identify differentially expressed genes. Often, small and negative expression levels were clipped-off to be equal to an arbitrarily chosen cutoff value before a statistical test is carried out. Then, there are two types of data: truncated values and original observations. The truncated values are not just another point on the continuum of possible values and, therefore, it is appropriate to combine two statistical tests in a two-part model rather than using standard statistical methods. A similar situation occurs when DNA methylation data are investigated. In that case, there are null values (undetectable methylation) and observed positive values. For these data, we propose a two-part permutation test. RESULTS: The proposed permutation test leads to smaller p-values in comparison to the original two-part test. We found this for both DNA methylation data and microarray data. With a simulation study we confirmed this result and could show that the two-part permutation test is, on average, more powerful. The new test also reduces, without any loss of power, to a standard test when there are no null or truncated values. CONCLUSION: The two-part permutation test can be used in routine analyses since it reduces to a standard test when there are positive values only. Further advantages of the new test are that it opens the possibility to use other test statistics to construct the two-part test and that it avoids the use of any asymptotic distribution. The latter advantage is particularly important for the analysis of microarrays since sample sizes are usually small.
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spelling pubmed-5516012005-03-04 Two-part permutation tests for DNA methylation and microarray data Neuhäuser, Markus Boes, Tanja Jöckel, Karl-Heinz BMC Bioinformatics Methodology Article BACKGROUND: One important application of microarray experiments is to identify differentially expressed genes. Often, small and negative expression levels were clipped-off to be equal to an arbitrarily chosen cutoff value before a statistical test is carried out. Then, there are two types of data: truncated values and original observations. The truncated values are not just another point on the continuum of possible values and, therefore, it is appropriate to combine two statistical tests in a two-part model rather than using standard statistical methods. A similar situation occurs when DNA methylation data are investigated. In that case, there are null values (undetectable methylation) and observed positive values. For these data, we propose a two-part permutation test. RESULTS: The proposed permutation test leads to smaller p-values in comparison to the original two-part test. We found this for both DNA methylation data and microarray data. With a simulation study we confirmed this result and could show that the two-part permutation test is, on average, more powerful. The new test also reduces, without any loss of power, to a standard test when there are no null or truncated values. CONCLUSION: The two-part permutation test can be used in routine analyses since it reduces to a standard test when there are positive values only. Further advantages of the new test are that it opens the possibility to use other test statistics to construct the two-part test and that it avoids the use of any asymptotic distribution. The latter advantage is particularly important for the analysis of microarrays since sample sizes are usually small. BioMed Central 2005-02-22 /pmc/articles/PMC551601/ /pubmed/15725357 http://dx.doi.org/10.1186/1471-2105-6-35 Text en Copyright © 2005 Neuhäuser et al; licensee BioMed Central Ltd.
spellingShingle Methodology Article
Neuhäuser, Markus
Boes, Tanja
Jöckel, Karl-Heinz
Two-part permutation tests for DNA methylation and microarray data
title Two-part permutation tests for DNA methylation and microarray data
title_full Two-part permutation tests for DNA methylation and microarray data
title_fullStr Two-part permutation tests for DNA methylation and microarray data
title_full_unstemmed Two-part permutation tests for DNA methylation and microarray data
title_short Two-part permutation tests for DNA methylation and microarray data
title_sort two-part permutation tests for dna methylation and microarray data
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC551601/
https://www.ncbi.nlm.nih.gov/pubmed/15725357
http://dx.doi.org/10.1186/1471-2105-6-35
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