NEMix: single-cell nested effects models for probabilistic pathway stimulation

PLoS Comput Biol. 2015 Apr 16;11(4):e1004078. doi: 10.1371/journal.pcbi.1004078. eCollection 2015 Apr.

Abstract

Nested effects models have been used successfully for learning subcellular networks from high-dimensional perturbation effects that result from RNA interference (RNAi) experiments. Here, we further develop the basic nested effects model using high-content single-cell imaging data from RNAi screens of cultured cells infected with human rhinovirus. RNAi screens with single-cell readouts are becoming increasingly common, and they often reveal high cell-to-cell variation. As a consequence of this cellular heterogeneity, knock-downs result in variable effects among cells and lead to weak average phenotypes on the cell population level. To address this confounding factor in network inference, we explicitly model the stimulation status of a signaling pathway in individual cells. We extend the framework of nested effects models to probabilistic combinatorial knock-downs and propose NEMix, a nested effects mixture model that accounts for unobserved pathway activation. We analyzed the identifiability of NEMix and developed a parameter inference scheme based on the Expectation Maximization algorithm. In an extensive simulation study, we show that NEMix improves learning of pathway structures over classical NEMs significantly in the presence of hidden pathway stimulation. We applied our model to single-cell imaging data from RNAi screens monitoring human rhinovirus infection, where limited infection efficiency of the assay results in uncertain pathway stimulation. Using a subset of genes with known interactions, we show that the inferred NEMix network has high accuracy and outperforms the classical nested effects model without hidden pathway activity. NEMix is implemented as part of the R/Bioconductor package 'nem' and available at www.cbg.ethz.ch/software/NEMix.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms*
  • Animals
  • Computer Simulation*
  • Humans
  • Likelihood Functions
  • Models, Biological*
  • Models, Statistical*
  • Proteins / metabolism*
  • Signal Transduction / physiology*
  • Software

Substances

  • Proteins

Grants and funding

CD, UG, and NB were supported by SystemsX.ch (www.systemsx.ch), the Swiss initiative in systems biology, under grant No. 51RT-0_126008 (InfectX), and CD and NB under grant No. 51RTP0_151029 (TargetInfectX). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.