AI Article Synopsis

  • Microarray experiments create large datasets where distinguishing valuable biological information from noise is crucial.
  • The analysis of gene expression requires considering variability and repeated measurements to identify differentially expressed genes effectively.
  • A new algorithm uses symbolic transformation to detect patterns of concerted gene behavior, improving the identification of relevant signals in compound datasets, and has shown promising results with rat liver gene expression data.

Article Abstract

Microarray experiments generate massive amounts of data, necessitating innovative algorithms to distinguish biologically relevant information from noise. Because the variability of gene expression data is an important factor in determining which genes are differentially expressed, analysis techniques that take into account repeated measurements are critically important. Additionally, the selection of informative genes is typically done by searching for the individual genes that vary the most across conditions. Yet because genes tend to act in groups rather than individually, it may be possible to glean more information from the data by searching specifically for concerted behavior in a set of genes. Applying a symbolic transformation to the gene expression data allows the detection overrepresented patterns in the data, in contrast to looking only for genes that exhibit maximal differential expression. These challenges are approached by introducing an algorithm based on a new symbolic representation that searches for concerted gene expression patterns; furthermore, the symbolic representation takes into account the variance in multiple replicates and can be applied to long time series data. The proposed algorithm's ability to discover biologically relevant signals in gene expression data is exhibited by applying it to three datasets that measure gene expression in the rat liver.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133780PMC
http://dx.doi.org/10.1089/omi.2010.0005DOI Listing

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