MuDCoD: multi-subject community detection in personalized dynamic gene networks from single-cell RNA sequencing

Author:

Şapcı Ali Osman Berk12ORCID,Lu Shan3,Yan Shuchen3,Ay Ferhat45ORCID,Tastan Oznur2ORCID,Keleş Sündüz36

Affiliation:

1. Bioinformatics and Systems Biology Graduate Program, University of California San Diego , La Jolla, CA 92093, United States

2. Faculty of Engineering and Natural Sciences, Sabancı University , Istanbul 34956, Turkey

3. Department of Statistics, University of Wisconsin-Madison , Madison, WI 53706, United States

4. Department of Pediatrics, University of California San Diego , La Jolla, CA 92093, United States

5. Centers for Autoimmunity, Inflammation and Cancer Immunotherapy, La Jolla Institute for Immunology , La Jolla, CA 92037, United States

6. Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison , Madison, WI 53706, United States

Abstract

Abstract Motivation With the wide availability of single-cell RNA-seq (scRNA-seq) technology, population-scale scRNA-seq datasets across multiple individuals and time points are emerging. While the initial investigations of these datasets tend to focus on standard analysis of clustering and differential expression, leveraging the power of scRNA-seq data at the personalized dynamic gene co-expression network level has the potential to unlock subject and/or time-specific network-level variation, which is critical for understanding phenotypic differences. Community detection from co-expression networks of multiple time points or conditions has been well-studied; however, none of the existing settings included networks from multiple subjects and multiple time points simultaneously. To address this, we develop Multi-subject Dynamic Community Detection (MuDCoD) for multi-subject community detection in personalized dynamic gene networks from scRNA-seq. MuDCoD builds on the spectral clustering framework and promotes information sharing among the networks of the subjects as well as networks at different time points. It clusters genes in the personalized dynamic gene networks and reveals gene communities that are variable or shared not only across time but also among subjects. Results Evaluation and benchmarking of MuDCoD against existing approaches reveal that MuDCoD effectively leverages apparent shared signals among networks of the subjects at individual time points, and performs robustly when there is no or little information sharing among the networks. Applications to population-scale scRNA-seq datasets of human-induced pluripotent stem cells during dopaminergic neuron differentiation and CD4+ T cell activation indicate that MuDCoD enables robust inference for identifying time-varying personalized gene modules. Our results illustrate how personalized dynamic community detection can aid in the exploration of subject-specific biological processes that vary across time. Availability and implementation MuDCoD is publicly available at https://github.com/bo1929/MuDCoD as a Python package. Implementation includes simulation and real-data experiments together with extensive documentation.

Funder

National Institutes of Health

Chan Zuckerberg Initiative

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference32 articles.

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