Identification of Gene Regulatory Networks from Single-Cell Expression Data.

Abstract

Single-cell RNAseq is an emerging technology that allows the quantification of gene expression in individual cells. In plants, single-cell sequencing technology has been applied to generate root cell expression maps under many experimental conditions. DAP-seq and ATAC-seq have also been used to generate genome-scale maps of protein-DNA interactions and open chromatin regions in plants. In this protocol, we describe a multistep computational pipeline for the integration of single-cell RNAseq data with DAP-seq and ATAC-seq data to predict regulatory networks and key regulatory genes. Our approach utilizes machine learning methods including feature selection and stability selection to identify candidate regulatory genes. The network generated by this pipeline can be used to provide a putative annotation of gene regulatory modules and to identify candidate transcription factors that could play a key role in specific cell types.