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Incorporation of biological knowledge into distance for clustering genes.

ABSTRACT: UNLABELLED:In this paper we propose a data based algorithm to marry existing biological knowledge (e.g., functional annotations of genes) with experimental data (gene expression profiles) in creating an overall dissimilarity that can be used with any clustering algorithm that uses a general dissimilarity matrix. We explore this idea with two publicly available gene expression data sets and functional annotations where the results are compared with the clustering results that uses only the experimental data. Although more elaborate evaluations might be called for, the present paper makes a strong case for utilizing existing biological information in the clustering process. AVAILABILITY:Supplement is available at www.somnathdatta.org/Supp/Bioinformation/appendix.pdf.

SUBMITTER: Boratyn GM

PROVIDER: S-EPMC1896054 | biostudies-literature | 2007 Apr

REPOSITORIES: biostudies-literature

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Incorporation of biological knowledge into distance for clustering genes.

Boratyn Grzegorz M GM Datta Susmita S Datta Somnath S

Bioinformation 20070410 10

<h4>Unlabelled</h4>In this paper we propose a data based algorithm to marry existing biological knowledge (e.g., functional annotations of genes) with experimental data (gene expression profiles) in creating an overall dissimilarity that can be used with any clustering algorithm that uses a general dissimilarity matrix. We explore this idea with two publicly available gene expression data sets and functional annotations where the results are compared with the clustering results that uses only th ...[more]

PMID: 17597929

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Project description:Background: Many tools used to analyze microarrays in different conditions have been described. However, the integration of the deregulated genes within coherent metabolic pathways is lacking. Currently no objective selection criterion, based on biological functions exists, to determine a threshold demonstrating that a gene is indeed differentially expressed. Methodology/Principal Findings: To improve transcriptomic analysis of microarrays, we propose a new statistical approach, which takes into account biological parameters. We present an iterative method to optimise the selection of differentially expressed gene in two experimental conditions. The stringency level of gene selection was associated simultaneously with the p-value of expression variation and the occurrence rate parameter, which is associated with the percentage of donors whose transcriptomic profile is similar. Our method intertwines stringency level settings, biological data and a knowledge database to highlight molecular interactions using networks and pathways. Analysis performed during iterations helped us select the optimal threshold required for the most pertinent selection of differently expressed genes. Conclusions/significance: We have applied this approach to the well documented mechanism of human macrophage response to lipopolysaccharide stimulation. For example, we thus verified that our method was able to determine with the highest degree of accuracy the best threshold for selecting genes, which are truly differentially expressed. Macrophages isolated from six heathy donnor was/or not stimulated. Paired data, i.e. LPS stimulated macrophages versus unstimulated macrophages from the same donor have been compared (eg, Donor1_LPS vs Donor1_NT; see processed data file linked below). The six comparaisons have been globaly analyse using two parameters, i.e. threshod and occurency, associated with a request of a database knowledge. Both parameters has been tune to define the best setting allowing to optimize the selection of differentially expressed genes

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Incorporation of biological knowledge into distance for clustering genes.

Publications

Incorporation of biological knowledge into distance for clustering genes.

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