Enhancer-driven gene regulatory networks inference from single-cell RNA-seq and ATAC-seq data

Author:

Li Yang12,Ma Anjun1234,Wang Yizhong5,Guo Qi12,Wang Cankun12,Fu Hongjun62,Liu Bingqiang5,Ma Qin1234

Affiliation:

1. Department of Biomedical Informatics , College of Medicine, , Columbus, OH 43210, United States

2. The Ohio State University , College of Medicine, , Columbus, OH 43210, United States

3. Pelotonia Institute for Immuno-Oncology , The James Comprehensive Cancer Center, , Columbus, OH 43210, United States

4. The Ohio State University , The James Comprehensive Cancer Center, , Columbus, OH 43210, United States

5. School of Mathematics, Shandong University , Jinan, Shandong 250100, China

6. Department of Neuroscience , College of Medicine, , Columbus, OH 43210, United States

Abstract

Abstract Deciphering the intricate relationships between transcription factors (TFs), enhancers, and genes through the inference of enhancer-driven gene regulatory networks (eGRNs) is crucial in understanding gene regulatory programs in a complex biological system. This study introduces STREAM, a novel method that leverages a Steiner forest problem model, a hybrid biclustering pipeline, and submodular optimization to infer eGRNs from jointly profiled single-cell transcriptome and chromatin accessibility data. Compared to existing methods, STREAM demonstrates enhanced performance in terms of TF recovery, TF–enhancer linkage prediction, and enhancer–gene relation discovery. Application of STREAM to an Alzheimer's disease dataset and a diffuse small lymphocytic lymphoma dataset reveals its ability to identify TF-enhancer–gene relations associated with pseudotime, as well as key TF-enhancer–gene relations and TF cooperation underlying tumor cells.

Funder

National Institute of General Medical Sciences

National Institutes of Health

National Science Foundation

Pelotonia Institute of Immuno-Oncology

Publisher

Oxford University Press (OUP)

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