Abstract

The use of single-cell transcriptomics has become a major approach to delineate cell subpopulations and the transitions between them. While various computational tools using different mathematical methods have been developed to infer clusters, marker genes, and cell lineage, none yet integrate these within a mathematical framework to perform multiple tasks coherently. Such coherence is critical for the inference of cell-cell communication, a major remaining challenge. Here, we present similarity matrix-based optimization for single-cell data analysis (SoptSC), in which unsupervised clustering, pseudotemporal ordering, lineage inference, and marker gene identification are inferred via a structured cell-to-cell similarity matrix. SoptSC then predicts cell-cell communication networks, enabling reconstruction of complex cell lineages that include feedback or feedforward interactions. Application of SoptSC to early embryonic development, epidermal regeneration, and hematopoiesis demonstrates robust identification of subpopulations, lineage relationships, and pseudotime, and prediction of pathway-specific cell communication patterns regulating processes of development and differentiation.

Keywords

BiologyInferenceComputational biologyTranscriptomeCell lineageLineage (genetic)GeneticsGene regulatory networkCellEvolutionary biologyGeneCellular differentiationGene expressionArtificial intelligenceComputer science

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Publication Info

Year
2019
Type
article
Volume
47
Issue
11
Pages
e66-e66
Citations
160
Access
Closed

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Shuxiong Wang, Matthew Karikomi, Adam L. MacLean et al. (2019). Cell lineage and communication network inference via optimization for single-cell transcriptomics. Nucleic Acids Research , 47 (11) , e66-e66. https://doi.org/10.1093/nar/gkz204

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DOI
10.1093/nar/gkz204