Graph-based autoencoder integrates spatial transcriptomics with chromatin images and identifies joint biomarkers for Alzheimer's disease.
Xinyi ZhangXiao WangG V ShivashankarCaroline UhlerPublished in: Nature communications (2022)
Tissue development and disease lead to changes in cellular organization, nuclear morphology, and gene expression, which can be jointly measured by spatial transcriptomic technologies. However, methods for jointly analyzing the different spatial data modalities in 3D are still lacking. We present a computational framework to integrate Spatial Transcriptomic data using over-parameterized graph-based Autoencoders with Chromatin Imaging data (STACI) to identify molecular and functional alterations in tissues. STACI incorporates multiple modalities in a single representation for downstream tasks, enables the prediction of spatial transcriptomic data from nuclear images in unseen tissue sections, and provides built-in batch correction of gene expression and tissue morphology through over-parameterization. We apply STACI to analyze the spatio-temporal progression of Alzheimer's disease and identify the associated nuclear morphometric and coupled gene expression features. Collectively, we demonstrate the importance of characterizing disease progression by integrating multiple data modalities and its potential for the discovery of disease biomarkers.
Keyphrases
- gene expression
- electronic health record
- dna methylation
- single cell
- big data
- convolutional neural network
- genome wide
- deep learning
- cognitive decline
- high resolution
- small molecule
- transcription factor
- working memory
- high throughput
- optical coherence tomography
- photodynamic therapy
- machine learning
- artificial intelligence
- neural network