Biologically Interpretable VAE with Supervision for Transcriptomics Data Under Ordinal Perturbations

Seyednami Niyakan, Xihaier Luo, Byung-Jun Yoon, Xiaoning Qian

Keywords: VAE, Interpretability, Ordinality, Pathway analysis, Perturbed Transcriptomics

TL;DR: We propose a novel deep learning framework, EXPORT (EXPlainable VAE for ORdinally perturbed Transcriptomics data), for analyzing ordinally perturbed transcriptomics data that can incorporate any biological pathway knowledge in the VAE latent space.

Abstract:

Latent variable models such as the Variational Auto-Encoders (VAEs) have shown impressive performance for inferring expression patterns for cell subtyping and biomarker identification from transcriptomics data. However, the limited interpretability of their latent variables obscures deriving meaningful biological understanding of cellular responses to different external and internal perturbations. We here propose a novel deep learning framework, EXPORT (EXPlainable VAE for ORdinally perturbed Transcriptomics data), for analyzing ordinally perturbed transcriptomics data that can incorporate any biological pathway knowledge in the VAE latent space. With the corresponding pathway-informed decoder, the learned latent expression patterns can be explained as pathway-level responses to perturbations, offering direct interpretability with biological understanding.
More importantly, we explicitly model the ordinal nature of many real-world perturbations into the EXPORT framework by training an auxiliary ordinal regressor neural network to capture corresponding expression changes in the VAE latent representations, for example under different dosage levels of radiation exposure. By incorporating ordinal constraints during the training of our proposed framework, we further enhance the model interpretability by guiding the VAE latent space to organize perturbation responses in a hierarchical manner. We demonstrate the utility of the inferred guided latent space for downstream tasks, such as identifying key regulatory pathways associated with specific perturbation changes by analyzing transcriptomics datasets on both bulk and single-cell data. Overall, we envision that our proposed approach can unravel unprecedented biological intricacies in cellular responses to various perturbations while bringing an additional layer of interpretability to biology-inspired deep learning models.

Submission Number: 37