Autoencoder Denoising for Network-Based Spatial Transcriptomics Data with Applications for Cell Signaling Estimation
Javaid, A.; Frost, H. R.
Show abstract
We propose an autoencoder-based framework for denoising networks estimated from Spatial Transcriptomics (ST) data for cell signaling analysis. Our method consists of an unsupervised encoder-decoder framework for denoising the network adjacency matrix and a supervised framework for cell signaling estimation. We validate our denoising component using the Frobenius norm metric for graphs simulated using the Barabasi-Albert (BA) and Erd[o]s-Renyi (ER) models against reconstructions generated using the singular value decomposition (SVD). We then validate the cell signaling estimates generated using the supervised component on real ST data for the Wnt3-Fzd1 and Ephb1-Efnb3 interactions. We report that our framework achieves better adjacency matrix reconstructions for superlinear BA and dense ER graphs and generates cell signaling estimates that are both regionally specific and biologically plausible. An important contribution of this work is the application of neural networks for network-based cell signaling estimation using ST data and the benchmarking of autoencoder versus SVD denoising for different graph models.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- RCFGL: Rapid Condition adaptive Fused Graphical Lasso and application to modeling brain region co-expression networks 96%
- Learning massive interpretable gene regulatory networks of the human brain by merging Bayesian Networks 96%
- Imputation of Spatially-resolved Transcriptomes by Graph-regularized Tensor Completion 95%
Similar papers in this journal
Similar papers in this journal
- Single-Cell Multi-Modal GAN (scMMGAN) reveals spatial patterns in single-cell data from triple negative breast cancer 95%
- hcga: Highly Comparative Graph Analysis for network phenotyping 94%
- scTenifoldNet: a machine learning workflow for constructing and comparing transcriptome-wide gene regulatory networks from single-cell data 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.