Abstract
The advance in high-throughput genomic technologies including microarrays has generated a tremendous amount of gene expression data for the entire genome. Deciphering transcriptional networks that convey information on members of gene clusters and cluster interactions is a crucial analysis task in the post-sequence era. Most of the existing analysis methods for large-scale genome-wide gene expression profiles involve several steps that often require human intervention. We propose a matrix theory-based approach to analyze the cross correlations of gene expression data in an entirely automatic and objective manner to eliminate the ambiguities and subjectivity inherent to human decisions. The correlations calculated from experimental measurements typically contain both genuine and random components. In the proposed approach, we remove the random component by testing the statistics of the eigenvalues of the correlation matrix against a null hypothesis - a truly correlation matrix obtained from mutually uncorrelated expression data series. Our investigation on the components of deviating eigenvectors using varimax orthogonal rotation reveals distinct functional modules. We apply the proposed approach to the publicly available yeast cycle expression data and produce a transcriptional network that consists of interacting functional modules. The experimental results nicely conform to those obtained in previously published literatures
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