Cluster stability scores for microarray data in cancer studies

<p>Abstract</p> <p>Background</p> <p>A potential benefit of profiling of tissue samples using microarrays is the generation of molecular fingerprints that will define subtypes of disease. Hierarchical clustering has been the primary analytical tool used to define diseas...

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Main Authors: Ghosh Debashis, Smolkin Mark
Format: Article
Language:English
Published: BMC 2003-09-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/4/36
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spelling doaj-ca0d4ce246644696bf0368a883ca72032020-11-24T23:04:56ZengBMCBMC Bioinformatics1471-21052003-09-01413610.1186/1471-2105-4-36Cluster stability scores for microarray data in cancer studiesGhosh DebashisSmolkin Mark<p>Abstract</p> <p>Background</p> <p>A potential benefit of profiling of tissue samples using microarrays is the generation of molecular fingerprints that will define subtypes of disease. Hierarchical clustering has been the primary analytical tool used to define disease subtypes from microarray experiments in cancer settings. Assessing cluster reliability poses a major complication in analyzing output from clustering procedures. While most work has focused on estimating the number of clusters in a dataset, the question of stability of individual-level clusters has not been addressed.</p> <p>Results</p> <p>We address this problem by developing cluster stability scores using subsampling techniques. These scores exploit the redundancy in biologically discriminatory information on the chip. Our approach is generic and can be used with any clustering method. We propose procedures for calculating cluster stability scores for situations involving both known and unknown numbers of clusters. We also develop cluster-size adjusted stability scores. The method is illustrated by application to data three cancer studies; one involving childhood cancers, the second involving B-cell lymphoma, and the final is from a malignant melanoma study.</p> <p>Availability</p> <p>Code implementing the proposed analytic method can be obtained at the second author's website.</p> http://www.biomedcentral.com/1471-2105/4/36
collection DOAJ
language English
format Article
sources DOAJ
author Ghosh Debashis
Smolkin Mark
spellingShingle Ghosh Debashis
Smolkin Mark
Cluster stability scores for microarray data in cancer studies
BMC Bioinformatics
author_facet Ghosh Debashis
Smolkin Mark
author_sort Ghosh Debashis
title Cluster stability scores for microarray data in cancer studies
title_short Cluster stability scores for microarray data in cancer studies
title_full Cluster stability scores for microarray data in cancer studies
title_fullStr Cluster stability scores for microarray data in cancer studies
title_full_unstemmed Cluster stability scores for microarray data in cancer studies
title_sort cluster stability scores for microarray data in cancer studies
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2003-09-01
description <p>Abstract</p> <p>Background</p> <p>A potential benefit of profiling of tissue samples using microarrays is the generation of molecular fingerprints that will define subtypes of disease. Hierarchical clustering has been the primary analytical tool used to define disease subtypes from microarray experiments in cancer settings. Assessing cluster reliability poses a major complication in analyzing output from clustering procedures. While most work has focused on estimating the number of clusters in a dataset, the question of stability of individual-level clusters has not been addressed.</p> <p>Results</p> <p>We address this problem by developing cluster stability scores using subsampling techniques. These scores exploit the redundancy in biologically discriminatory information on the chip. Our approach is generic and can be used with any clustering method. We propose procedures for calculating cluster stability scores for situations involving both known and unknown numbers of clusters. We also develop cluster-size adjusted stability scores. The method is illustrated by application to data three cancer studies; one involving childhood cancers, the second involving B-cell lymphoma, and the final is from a malignant melanoma study.</p> <p>Availability</p> <p>Code implementing the proposed analytic method can be obtained at the second author's website.</p>
url http://www.biomedcentral.com/1471-2105/4/36
work_keys_str_mv AT ghoshdebashis clusterstabilityscoresformicroarraydataincancerstudies
AT smolkinmark clusterstabilityscoresformicroarraydataincancerstudies
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