TL;DR
This paper introduces a method to derive individual sample-specific gene regulatory networks from aggregate models, enabling detailed analysis of heterogeneity in biological data for advancing precision medicine.
Contribution
The paper presents a novel approach to reverse engineer sample-specific networks from aggregate models, addressing heterogeneity in gene regulation analysis.
Findings
Accurately reconstructs sample-specific networks from aggregate models.
Demonstrates applicability on simulated, yeast, and human data.
Reveals network topology changes not visible in expression data.
Abstract
Biological systems are driven by intricate interactions among the complex array of molecules that comprise the cell. Many methods have been developed to reconstruct network models of those interactions. These methods often draw on large numbers of samples with measured gene expression profiles to infer connections between genes (or gene products). The result is an aggregate network model representing a single estimate for the likelihood of each interaction, or "edge," in the network. While informative, aggregate models fail to capture the heterogeneity that is represented in any population. Here we propose a method to reverse engineer sample-specific networks from aggregate network models. We demonstrate the accuracy and applicability of our approach in several data sets, including simulated data, microarray expression data from synchronized yeast cells, and RNA-seq data collected from…
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