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A contrastive learning approach to integrate spatial transcriptomics and histological images. | LitMetric

A contrastive learning approach to integrate spatial transcriptomics and histological images.

Comput Struct Biotechnol J

Department of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.

Published: December 2024

AI Article Synopsis

  • The growth of spatially resolved transcriptomics technology offers new insights into tissue structure, but integrating diverse data types remains difficult.
  • A new model called ConGcR uses contrastive learning to combine gene expression, spatial location, and tissue morphology data for better representation and identification of tissue architecture.
  • Validation on various tissue samples demonstrated that ConGcR, enhanced by a graph auto-encoder (ConGaR), produced superior embeddings, improving the accuracy of tissue architecture identification compared to existing methods.

Article Abstract

The rapid growth of spatially resolved transcriptomics technology provides new perspectives on spatial tissue architecture. Deep learning has been widely applied to derive useful representations for spatial transcriptome analysis. However, effectively integrating spatial multi-modal data remains challenging. Here, we present ConGcR, a contrastive learning-based model for integrating gene expression, spatial location, and tissue morphology for data representation and spatial tissue architecture identification. Graph convolution and ResNet were used as encoders for gene expression with spatial location and histological image inputs, respectively. We further enhanced ConGcR with a graph auto-encoder as ConGaR to better model spatially embedded representations. We validated our models using 16 human brains, four chicken hearts, eight breast tumors, and 30 human lung spatial transcriptomics samples. The results showed that our models generated more effective embeddings for obtaining tissue architectures closer to the ground truth than other methods. Overall, our models not only can improve tissue architecture identification's accuracy but also may provide valuable insights and effective data representation for other tasks in spatial transcriptome analyses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11068546PMC
http://dx.doi.org/10.1016/j.csbj.2024.04.039DOI Listing

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