Abstract
AbstractTissue 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.
Funder
Eric and Wendy Schmidt Center at the Broad Institute
U.S. Department of Health & Human Services | National Institutes of Health
Searle Scholarship Cabot Professorship at MIT Edward Scolnick Professorship at the Broad Institute Merkin Institute Fellowship Ono Pharma Breakthrough Science Initiative Award
Eidgenössische Technische Hochschule Zürich
National Science Foundation
United States Department of Defense | United States Navy | Office of Naval Research
Simons Foundation
MIT-IBM Watson AI Lab MIT J-Clinic for Machine Learning and Health
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary
Cited by
27 articles.
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