Benchmarking variational AutoEncoders on cancer transcriptomics data

PLoS One. 2023 Oct 5;18(10):e0292126. doi: 10.1371/journal.pone.0292126. eCollection 2023.

Abstract

Deep generative models, such as variational autoencoders (VAE), have gained increasing attention in computational biology due to their ability to capture complex data manifolds which subsequently can be used to achieve better performance in downstream tasks, such as cancer type prediction or subtyping of cancer. However, these models are difficult to train due to the large number of hyperparameters that need to be tuned. To get a better understanding of the importance of the different hyperparameters, we examined six different VAE models when trained on TCGA transcriptomics data and evaluated on the downstream tasks of cluster agreement with cancer subtypes and survival analysis. We studied the effect of the latent space dimensionality, learning rate, optimizer, initialization and activation function on the quality of subsequent downstream tasks on the TCGA samples. We found β-TCVAE and DIP-VAE to have a good performance, on average, despite being more sensitive to hyperparameters selection. Based on these experiments, we derived recommendations for selecting the different hyperparameters settings. To ensure generalization, we tested all hyperparameter configurations on the GTEx dataset. We found a significant correlation (ρ = 0.7) between the hyperparameter effects on clustering performance in the TCGA and GTEx datasets. This highlights the robustness and generalizability of our recommendations. In addition, we examined whether the learned latent spaces capture biologically relevant information. Hereto, we measured the correlation and mutual information of the different representations with various data characteristics such as gender, age, days to metastasis, immune infiltration, and mutation signatures. We found that for all models the latent factors, in general, do not uniquely correlate with one of the data characteristics nor capture separable information in the latent factors even for models specifically designed for disentanglement.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benchmarking*
  • Cluster Analysis
  • Gene Expression Profiling
  • Humans
  • Neoplasms* / genetics
  • Transcriptome

Grants and funding

ME,MR: European Union’ H2020 research and innovation program under the MSCA grant agreement [861190 (PAVE)]: (https://pave-cancer.eu/EU_Projects/PAVE.nsf/xStart_Basic.xsp) TA,AM,MR: NWO Gravitation project: BRAINSCAPES: A Roadmap from Neurogenetics to Neurobiology (NWO: 024.004.012) SM&MR:have received funding from the Convergence Health & Technology program of the Delft University of Technology and Erasmus Medical Center. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.