Nature MethodsBioinformaticsPeer-reviewed journal article
Discovering novel cell types across heterogeneous single-cell experiments
Maria BrbićiD, Marinka ŽitnikiD, Sheng WangiD, Angela Oliveira PiscoiD, Russ Biagio AltmaniD, Spyros DarmanisiD, Jure LeskoveciD
Abstract
Although tremendous effort has been put into cell type annotation and classification, identification of previously uncharacterized cell types in heterogeneous single-cell RNA-seq data remains a challenge. Here we present MARS, a meta-learning approach for identifying and annotating known as well as novel cell types. MARS overcomes the heterogeneity of cell types by transferring latent cell representations across multiple datasets. MARS uses deep learning to learn a cell embedding function as well as a set of landmarks in the cell embedding space. The method annotates cells by probabilistically defining a cell type based on nearest landmarks in the embedding space. MARS has a unique ability to discover cell types that have never been seen before and annotate experiments that are yet unannotated. We apply MARS to a large aging cell atlas of 23 tissues covering the life span of a mouse. MARS accurately identifies cell types, even when it has never seen them before. Further, the method automatically generates interpretable names for novel cell types. Remarkably, MARS estimates meaningful cell-type-specific signatures of aging and visualizes them as trajectories reflecting temporal relationships of cells in a tissue.
- organism: mouse
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: clustering
- research focus: benchmarking
- approach: deep learning
- approach: statistical model
- Citations
- 143
- FWCI
- 6.89
- Field percentile
- top 2%
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