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.
Toward terminological clarity in digital biomarker research
Digital biomarker research has generated thousands of publications demonstrating associations between sensor-derived measures and clinical conditions, yet clinical adoption remains negligible. We identify a foundational



