siVAE: interpretable deep generative models for single-cell transcriptomes.

Journal: Genome biology
Published Date:

Abstract

Neural networks such as variational autoencoders (VAE) perform dimensionality reduction for the visualization and analysis of genomic data, but are limited in their interpretability: it is unknown which data features are represented by each embedding dimension. We present siVAE, a VAE that is interpretable by design, thereby enhancing downstream analysis tasks. Through interpretation, siVAE also identifies gene modules and hubs without explicit gene network inference. We use siVAE to identify gene modules whose connectivity is associated with diverse phenotypes such as iPSC neuronal differentiation efficiency and dementia, showcasing the wide applicability of interpretable generative models for genomic data analysis.

Authors

  • Yongin Choi
    Graduate Group in Biomedical Engineering, University of California, Davis, Davis, CA, USA.
  • Ruoxin Li
    Department of Chemistry, Tsinghua University, Beijing 100084, China.
  • Gerald Quon
    Department of Molecular and Cellular Biology, University of California-Davis, Davis, CA,USA.