4.6 Article

A novel method for cross-species gene expression analysis

期刊

BMC BIOINFORMATICS
卷 14, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1471-2105-14-70

关键词

Gene expression; Evolution; Meta-analysis; Orthologs; Paralogs; Microarray; RNA-seq

资金

  1. Life Science Area of Advance at Chalmers University of Technology, Sweden
  2. Swedish Research Council (VR)
  3. Foundation for Strategic Environmental Research (MISTRA)
  4. Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS)
  5. Swedish Society for Medical Research (SSMF)
  6. Gothenburg Bioinformatics Network (GOTBIN)

向作者/读者索取更多资源

Background: Analysis of gene expression from different species is a powerful way to identify evolutionarily conserved transcriptional responses. However, due to evolutionary events such as gene duplication, there is no one-to-one correspondence between genes from different species which makes comparison of their expression profiles complex. Results: In this paper we describe a new method for cross-species meta-analysis of gene expression. The method takes the homology structure between compared species into account and can therefore compare expression data from genes with any number of orthologs and paralogs. A simulation study shows that the proposed method results in a substantial increase in statistical power compared to previously suggested procedures. As a proof of concept, we analyzed microarray data from heat stress experiments performed in eight species and identified several well-known evolutionarily conserved transcriptional responses. The method was also applied to gene expression profiles from five studies of estrogen exposed fish and both known and potentially novel responses were identified. Conclusions: The method described in this paper will further increase the potential and reliability of meta-analysis of gene expression profiles from evolutionarily distant species. The method has been implemented in R and is freely available at http://bioinformatics.math.chalmers.se/Xspecies/.

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