4.7 Review

The effect of tissue composition on gene co-expression

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 22, Issue 1, Pages 127-139

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbz135

Keywords

transcriptomics; deconvolution; cell-types; induced covariance; co-expression; tissue composition

Funding

  1. National Institutes of Health [R00HG006853, R01HL137811, T32ES007271, HHSN272201200005C]
  2. University of Rochester CTSA [UL1TR002001]
  3. National Center for Advancing Translational Sciences of the National Institutes of Health

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This study illustrates the effect of variable cell-type composition on correlation-based network estimation and demonstrates that a deconvolution method can be applied to two component cell-type mixtures. The results suggest that uncorrelated cell-type-specific markers are ideally suited for deconvoluting the expression and co-expression patterns of an individual cell type.
Variable cellular composition of tissue samples represents a significant challenge for the interpretation of genomic profiling studies. Substantial effort has been devoted to modeling and adjusting for compositional differences when estimating differential expression between sample types. However, relatively little attention has been given to the effect of tissue composition on co-expression estimates. In this study, we illustrate the effect of variable cell-type composition on correlation-based network estimation and provide a mathematical decomposition of the tissue-level correlation. We show that a class of deconvolution methods developed to separate tumor and stromal signatures can be applied to two component cell-type mixtures. In simulated and real data, we identify conditions in which a deconvolution approach would be beneficial. Our results suggest that uncorrelated cell-type-specific markers are ideally suited to deconvolute both the expression and co-expression patterns of an individual cell type. We provide a Shiny application for users to interactively explore the effect of cell-type composition on correlation-based co-expression estimation for any cell types of interest.

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