Publication | Open Access
DeepVelo: Deep Learning extends RNA velocity to multi-lineage systems with cell-specific kinetics
24
Citations
28
References
2022
Year
Unknown Venue
EngineeringTranscriptomics TechnologyGene Regulatory NetworkCell DifferentiationTrajectory AnalysisTranscriptional RegulationTime-dependent KineticsSingle Cell SequencingRna BiologyTranslatomicsSingle-cell GenomicsDeep LearningSingle-cell AnalysisBioinformaticsFunctional GenomicsEpigenetic RegulationCell BiologyGene ExpressionBiologyDevelopmental BiologyRna VelocityComputational BiologySystems BiologyMedicineCell-specific KineticsCell DevelopmentNon-coding Rna
1 Abstract The introduction of RNA velocity in single-cell studies has opened new ways of examining cell differentiation and tissue development. Existing RNA velocity estimation methods rely on strong assumptions of predefined dynamics and cell-agnostic constant transcriptional kinetic rates, which are often violated in complex and heterogeneous single-cell RNA sequencing (scRNA-seq) data. To overcome these limitations, we propose DeepVelo, a novel method that estimates the cell-specific dynamics of splicing kinetics using Graph Convolution Networks (GCNs). DeepVelo generalizes RNA velocity to cell populations containing time-dependent kinetics and multiple lineages, which are common in developmental and pathological systems. We applied DeepVelo to disentangle multifaceted kinetics in the processes of dentate gyrus neurogenesis, pancreatic endocrinogenesis, and hindbrain development. The method infers time-varying cellular rates of transcription, splicing and degradation, recovers each cell’s stage in the underlying differentiation process, and detects functionally relevant driver genes regulating these processes. DeepVelo relaxes the constraints of previous techniques, facilitates the study of more complex differentiation and lineage decision events in heterogeneous scRNA-seq data, and is more computationally efficient than previous techniques.
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