Gene trajectory inference for single-cell data by optimal transport metrics.
Rihao QuXiuyuan ChengEsen SefikJay S Stanley IiiBoris LandaFrancesco StrinoSarah PlattJames GarritanoIan D OdellRonald CoifmanRichard A FlavellPeggy MyungYuval KlugerPublished in: Nature biotechnology (2024)
Single-cell RNA sequencing has been widely used to investigate cell state transitions and gene dynamics of biological processes. Current strategies to infer the sequential dynamics of genes in a process typically rely on constructing cell pseudotime through cell trajectory inference. However, the presence of concurrent gene processes in the same group of cells and technical noise can obscure the true progression of the processes studied. To address this challenge, we present GeneTrajectory, an approach that identifies trajectories of genes rather than trajectories of cells. Specifically, optimal transport distances are calculated between gene distributions across the cell-cell graph to extract gene programs and define their gene pseudotemporal order. Here we demonstrate that GeneTrajectory accurately extracts progressive gene dynamics in myeloid lineage maturation. Moreover, we show that GeneTrajectory deconvolves key gene programs underlying mouse skin hair follicle dermal condensate differentiation that could not be resolved by cell trajectory approaches. GeneTrajectory facilitates the discovery of gene programs that control the changes and activities of biological processes.
Keyphrases
- single cell
- genome wide
- rna seq
- genome wide identification
- copy number
- high throughput
- cell therapy
- public health
- genome wide analysis
- depressive symptoms
- transcription factor
- small molecule
- dendritic cells
- immune response
- acute myeloid leukemia
- signaling pathway
- air pollution
- deep learning
- anti inflammatory
- rectal cancer