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In Journal of computational biology : a journal of computational molecular cell biology ; h5-index 0.0

Single-cell transcriptomics offers a tool to study the diversity of cell phenotypes through snapshots of the abundance of mRNA in individual cells. Often there is additional information available besides the single-cell gene expression counts, such as bulk transcriptome data from the same tissue, or quantification of surface protein levels from the same cells. In this study, we propose models based on the Bayesian deep learning approach, where protein quantification, available as CITE-seq counts, from the same cells is used to constrain the learning process, thus forming a SemI-SUpervised generative Autoencoder (SISUA) model. The generative model is based on the deep variational autoencoder (VAE) neural network architecture.

Ngo Trong Trung, Mehtonen Juha, González Gerardo, Kramer Roger, Hautamäki Ville, Heinäniemi Merja


autoencoder, deep learning, generative, protein, semisupervised, single-cell, variational