Interpretable factor models of single-cell RNA-seq via variational autoencoders.
basic_science · Level V
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- Record sourced from PubMed, PMID 32176273.
- Also identified by DOI 10.1093/bioinformatics/btaa169 and PMC identifier 7267837.
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Abstract
Single-cell RNA-seq makes possible the investigation of variability in gene expression among cells, and dependence of variation on cell type. Statistical inference methods for such analyses must be scalable, and ideally interpretable. We present an approach based on a modification of a recently published highly scalable variational autoencoder framework that provides interpretability without sacrificing much accuracy. We demonstrate that our approach enables identification of gene programs in massive datasets. Our strategy, namely the learning of factor models with the auto-encoding variational Bayes framework, is not domain specific and may be useful for other applications. The factor model is available in the scVI package hosted at https://github.com/YosefLab/scVI/. v@nxn.se. Supplementary data are available at Bioinformatics online.
Medical subject headings
- RNA-Seq
- Single-Cell Analysis