Abstract
Single-cell RNA-seq technologies enable high throughput gene expression measurement of individual cells, and allow the discovery of heterogeneity within cell populations. Measurement of cell-to-cell gene expression similarity is critical to identification, visualization and analysis of cell populations. However, single-cell data introduce challenges to conventional measures of gene expression similarity because of the high level of noise, outliers and dropouts. Here, we propose a novel similarity-learning framework, SIMLR (single-cell interpretation via multi-kernel learning), which learns an appropriate distance metric from the data for dimension reduction, clustering and visualization applications. Benchmarking against state-of-the-art methods for these applications, we used SIMLR to re-analyse seven representative single-cell data sets, including high-throughput droplet-based data sets with tens of thousands of cells. We show that SIMLR greatly improves clustering sensitivity and accuracy, as well as the visualization and interpretability of the data.
Abbreviations
- SIMLR
- Single-cell Interpretation via multi-kernel enhanced similarity learning
- mESCs
- mouse embryonic stem cells
- NMI
- Normalized mutual information
- NNE
- Nearest neighbor error
- MDS
- Multidimensional scaling
- FA
- Factor analysis
- PCA
- Principal component analysis
- PPCA
- Probabilistic principal components analysis
- ZIFA
- Zero-inflated factor analysis
- SNE
- Stochastic neighbor embedding
- t-SNE
- t-distributed stochastic neighbor embedding