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Interpretable factor models of single-cell RNA-seq via variational autoencoders

MOTIVATION: 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. RESULTS: We present an approach based on a modificati...

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Detalles Bibliográficos
Autores principales: Svensson, Valentine, Gayoso, Adam, Yosef, Nir, Pachter, Lior
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267837/
https://www.ncbi.nlm.nih.gov/pubmed/32176273
http://dx.doi.org/10.1093/bioinformatics/btaa169
Descripción
Sumario:MOTIVATION: 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. RESULTS: 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. AVAILABILITY AND IMPLEMENTATION: The factor model is available in the scVI package hosted at https://github.com/YosefLab/scVI/. CONTACT: v@nxn.se SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.