The effect of tissue composition on gene co-expression

被引:15
作者
Zhang, Yun [1 ,2 ]
Cuerdo, Jonavelle [3 ]
Halushka, Marc K. [4 ]
McCall, Matthew N. [5 ]
机构
[1] J Craig Venter Inst, Dept Informat, Rockville, MD USA
[2] Univ Rochester, Med Ctr, Rochester, NY 14627 USA
[3] Univ Rochester, Rochester, NY 14627 USA
[4] Johns Hopkins Univ, Dept Pathol, Baltimore, MD 21218 USA
[5] Dept Biostat & Computat Biol & Biomed Genet, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
transcriptomics; deconvolution; cell-types; induced covariance; co-expression; tissue composition; COMPUTATIONAL PURIFICATION; REGULATORY NETWORKS; EXPRESSION; DECONVOLUTION; INFORMATION; ALGORITHM; IMPACT;
D O I
10.1093/bib/bbz135
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:127 / 139
页数:13
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