Cell type-specific gene regulatory network inference from single cell transcriptomics with ctOTVelo

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The paper studies how to infer gene regulatory networks from single-cell transcriptomics while accounting for the fact that gene regulation changes over time and can differ across cell types. It introduces ctOTVelo, an extension of the authors’ previous work that uses cell type labels or cell type proportions during GRN inference, and evaluates it on time-stamped and pseudotime-stamped transcriptomics. The key finding is that ctOTVelo achieves state-of-the-art performance for GRN prediction and can generate cell type-specific GRNs for downstream cell type resolution of regulatory relationships. The provided text does not state explicit limitations, but it notes the method depends on available time structure (timepoints or pseudotime) and cell-type information for inference. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract Inferring gene regulatory networks (GRNs) from gene expression is a crucial task for understanding functional relationships. Gene expression data (transcriptomics) provide a snapshot of gene activity, encoding information about gene regulatory relationships. However, gene regulation is a dynamic process, modulating across time and with different cell types. Temporal GRN inference methods aim to capture these dynamics by utilizing time-stamped transcriptomics, gene expression data of similar samples captured across discrete timepoints, or pseudotime transcriptomics, computationally ordering cells based on an inferred trajectory. These methods can estimate constant or temporal gene regulatory relationships, but may not capture finer, cell type specific relationships. We propose ctOTVelo, an extension to our previous work to account for cell type specificity during GRN inference. ctOTVelo incorporates cell type labels or proportions when inferring the GRN from single cell transcriptomics data. Our methods achieve state-of-the-art performance in GRN prediction in time-stamped and pseudotime-stamped transcriptomics. Furthermore, ctOTVelo is able to generate cell type specific GRNs, allowing cell type resolution analysis of gene regulatory relationships. Competing Interest Statement The authors have declared no competing interest. Footnotes zhaow{at}wfu.edu ying_ma{at}brown.edu bjorn_sandstede{at}brown.edu ritambhara{at}brown.edu

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last seen: 2026-05-20T01:45:00.602351+00:00