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Clustering gene expression data with a penalized graph-based metric
BACKGROUND: The search for cluster structure in microarray datasets is a base problem for the so-called "-omic sciences". A difficult problem in clustering is how to handle data with a manifold structure, i.e. data that is not shaped in the form of compact clouds of points, forming arbitra...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023695/ https://www.ncbi.nlm.nih.gov/pubmed/21205299 http://dx.doi.org/10.1186/1471-2105-12-2 |
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author | Bayá, Ariel E Granitto, Pablo M |
author_facet | Bayá, Ariel E Granitto, Pablo M |
author_sort | Bayá, Ariel E |
collection | PubMed |
description | BACKGROUND: The search for cluster structure in microarray datasets is a base problem for the so-called "-omic sciences". A difficult problem in clustering is how to handle data with a manifold structure, i.e. data that is not shaped in the form of compact clouds of points, forming arbitrary shapes or paths embedded in a high-dimensional space, as could be the case of some gene expression datasets. RESULTS: In this work we introduce the Penalized k-Nearest-Neighbor-Graph (PKNNG) based metric, a new tool for evaluating distances in such cases. The new metric can be used in combination with most clustering algorithms. The PKNNG metric is based on a two-step procedure: first it constructs the k-Nearest-Neighbor-Graph of the dataset of interest using a low k-value and then it adds edges with a highly penalized weight for connecting the subgraphs produced by the first step. We discuss several possible schemes for connecting the different sub-graphs as well as penalization functions. We show clustering results on several public gene expression datasets and simulated artificial problems to evaluate the behavior of the new metric. CONCLUSIONS: In all cases the PKNNG metric shows promising clustering results. The use of the PKNNG metric can improve the performance of commonly used pairwise-distance based clustering methods, to the level of more advanced algorithms. A great advantage of the new procedure is that researchers do not need to learn a new method, they can simply compute distances with the PKNNG metric and then, for example, use hierarchical clustering to produce an accurate and highly interpretable dendrogram of their high-dimensional data. |
format | Text |
id | pubmed-3023695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30236952011-01-20 Clustering gene expression data with a penalized graph-based metric Bayá, Ariel E Granitto, Pablo M BMC Bioinformatics Methodology Article BACKGROUND: The search for cluster structure in microarray datasets is a base problem for the so-called "-omic sciences". A difficult problem in clustering is how to handle data with a manifold structure, i.e. data that is not shaped in the form of compact clouds of points, forming arbitrary shapes or paths embedded in a high-dimensional space, as could be the case of some gene expression datasets. RESULTS: In this work we introduce the Penalized k-Nearest-Neighbor-Graph (PKNNG) based metric, a new tool for evaluating distances in such cases. The new metric can be used in combination with most clustering algorithms. The PKNNG metric is based on a two-step procedure: first it constructs the k-Nearest-Neighbor-Graph of the dataset of interest using a low k-value and then it adds edges with a highly penalized weight for connecting the subgraphs produced by the first step. We discuss several possible schemes for connecting the different sub-graphs as well as penalization functions. We show clustering results on several public gene expression datasets and simulated artificial problems to evaluate the behavior of the new metric. CONCLUSIONS: In all cases the PKNNG metric shows promising clustering results. The use of the PKNNG metric can improve the performance of commonly used pairwise-distance based clustering methods, to the level of more advanced algorithms. A great advantage of the new procedure is that researchers do not need to learn a new method, they can simply compute distances with the PKNNG metric and then, for example, use hierarchical clustering to produce an accurate and highly interpretable dendrogram of their high-dimensional data. BioMed Central 2011-01-04 /pmc/articles/PMC3023695/ /pubmed/21205299 http://dx.doi.org/10.1186/1471-2105-12-2 Text en Copyright ©2011 Bayá and Granitto; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Bayá, Ariel E Granitto, Pablo M Clustering gene expression data with a penalized graph-based metric |
title | Clustering gene expression data with a penalized graph-based metric |
title_full | Clustering gene expression data with a penalized graph-based metric |
title_fullStr | Clustering gene expression data with a penalized graph-based metric |
title_full_unstemmed | Clustering gene expression data with a penalized graph-based metric |
title_short | Clustering gene expression data with a penalized graph-based metric |
title_sort | clustering gene expression data with a penalized graph-based metric |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023695/ https://www.ncbi.nlm.nih.gov/pubmed/21205299 http://dx.doi.org/10.1186/1471-2105-12-2 |
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