Abstract
Although advances in single-cell technologies have enabled the characterization of multiple omics profiles in individual cells, extracting functional and mechanistic insights from such information remains a major challenge. Here, we present scapGNN, a graph neural network (GNN)-based framework that creatively transforms sparse single-cell profile data into the stable gene–cell association network for inferring single-cell pathway activity scores and identifying cell phenotype–associated gene modules from single-cell multi-omics data. Systematic benchmarking demonstrated that scapGNN was more accurate, robust, and scalable than state-of-the-art methods in various downstream single-cell analyses such as cell denoising, batch effect removal, cell clustering, cell trajectory inference, and pathway or gene module identification. scapGNN was developed as a systematic R package that can be flexibly extended and enhanced for existing analysis processes. It provides a new analytical platform for studying single cells at the pathway and network levels.
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CITATION STYLE
Han, X., Wang, B., Situ, C., Qi, Y., Zhu, H., Li, Y., & Guo, X. (2023). scapGNN: A graph neural network–based framework for active pathway and gene module inference from single-cell multi-omics data. PLoS Biology, 21(11 November). https://doi.org/10.1371/journal.pbio.3002369
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