Abstract
Complex tissues are composed of a large number of different types of cells, each involved in a multitude of biological processes. Consequently, an important component to understanding such processes is understanding the cell-type composition of the tissues. Estimating cell-type composition using high-throughput gene expression data is known as cell-type deconvolution. In this paper we first summarize the extensive deconvolution literature by identifying a common regression-like approach to deconvolution. We call this approach the unified deconvolution-as-regression (UDAR) framework. While methods that fall under this framework all use a similar model, they fit using data on different scales. Two popular scales for gene expression data are logarithmic and linear. Unfortunately, each of these scales has problems in the UDAR framework. Using log-scale gene expressions proposes a biologically implausible model and using linear-scale gene expressions will lead to statistically inefficient estimators. To explore ways to address these issues, in this paper we consider how deconvolution methods may use an adjusted model that is a hybrid of the two scales. In analysis on simulations as well as a collection of eleven real benchmark datasets, we find a prototypical hybrid-scale adjustment to the UDAR framework improves statistical efficiency and robustness. More broadly, we believe these hybrid-scale modeling principles may be incorporated into many existing deconvolution methods.
Acknowledgments
The authors gratefully acknowledge support from the National Science Foundation (grant no. DMS-1646108).
Citation
Gregory J. Hunt. Johann A. Gagnon-Bartsch. "The role of scale in the estimation of cell-type proportions." Ann. Appl. Stat. 15 (1) 270 - 286, March 2021. https://doi.org/10.1214/20-AOAS1395
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