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Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles
BACKGROUND: The hierarchical clustering tree (HCT) with a dendrogram [1] and the singular value decomposition (SVD) with a dimension-reduced representative map [2] are popular methods for two-way sorting the gene-by-array matrix map employed in gene expression profiling. While HCT dendrograms tend t...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2322988/ https://www.ncbi.nlm.nih.gov/pubmed/18366693 http://dx.doi.org/10.1186/1471-2105-9-155 |
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author | Tien, Yin-Jing Lee, Yun-Shien Wu, Han-Ming Chen, Chun-Houh |
author_facet | Tien, Yin-Jing Lee, Yun-Shien Wu, Han-Ming Chen, Chun-Houh |
author_sort | Tien, Yin-Jing |
collection | PubMed |
description | BACKGROUND: The hierarchical clustering tree (HCT) with a dendrogram [1] and the singular value decomposition (SVD) with a dimension-reduced representative map [2] are popular methods for two-way sorting the gene-by-array matrix map employed in gene expression profiling. While HCT dendrograms tend to optimize local coherent clustering patterns, SVD leading eigenvectors usually identify better global grouping and transitional structures. RESULTS: This study proposes a flipping mechanism for a conventional agglomerative HCT using a rank-two ellipse (R2E, an improved SVD algorithm for sorting purpose) seriation by Chen [3] as an external reference. While HCTs always produce permutations with good local behaviour, the rank-two ellipse seriation gives the best global grouping patterns and smooth transitional trends. The resulting algorithm automatically integrates the desirable properties of each method so that users have access to a clustering and visualization environment for gene expression profiles that preserves coherent local clusters and identifies global grouping trends. CONCLUSION: We demonstrate, through four examples, that the proposed method not only possesses better numerical and statistical properties, it also provides more meaningful biomedical insights than other sorting algorithms. We suggest that sorted proximity matrices for genes and arrays, in addition to the gene-by-array expression matrix, can greatly aid in the search for comprehensive understanding of gene expression structures. Software for the proposed methods can be obtained at . |
format | Text |
id | pubmed-2322988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23229882008-04-18 Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles Tien, Yin-Jing Lee, Yun-Shien Wu, Han-Ming Chen, Chun-Houh BMC Bioinformatics Methodology Article BACKGROUND: The hierarchical clustering tree (HCT) with a dendrogram [1] and the singular value decomposition (SVD) with a dimension-reduced representative map [2] are popular methods for two-way sorting the gene-by-array matrix map employed in gene expression profiling. While HCT dendrograms tend to optimize local coherent clustering patterns, SVD leading eigenvectors usually identify better global grouping and transitional structures. RESULTS: This study proposes a flipping mechanism for a conventional agglomerative HCT using a rank-two ellipse (R2E, an improved SVD algorithm for sorting purpose) seriation by Chen [3] as an external reference. While HCTs always produce permutations with good local behaviour, the rank-two ellipse seriation gives the best global grouping patterns and smooth transitional trends. The resulting algorithm automatically integrates the desirable properties of each method so that users have access to a clustering and visualization environment for gene expression profiles that preserves coherent local clusters and identifies global grouping trends. CONCLUSION: We demonstrate, through four examples, that the proposed method not only possesses better numerical and statistical properties, it also provides more meaningful biomedical insights than other sorting algorithms. We suggest that sorted proximity matrices for genes and arrays, in addition to the gene-by-array expression matrix, can greatly aid in the search for comprehensive understanding of gene expression structures. Software for the proposed methods can be obtained at . BioMed Central 2008-03-20 /pmc/articles/PMC2322988/ /pubmed/18366693 http://dx.doi.org/10.1186/1471-2105-9-155 Text en Copyright © 2008 Tien 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 | Methodology Article Tien, Yin-Jing Lee, Yun-Shien Wu, Han-Ming Chen, Chun-Houh Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
title | Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
title_full | Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
title_fullStr | Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
title_full_unstemmed | Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
title_short | Methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
title_sort | methods for simultaneously identifying coherent local clusters with smooth global patterns in gene expression profiles |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2322988/ https://www.ncbi.nlm.nih.gov/pubmed/18366693 http://dx.doi.org/10.1186/1471-2105-9-155 |
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