DNA-GPS: A theoretical framework for optics-free spatial genomics and synthesis of current methods
While single-cell sequencing technologies provide unprecedented insights into genomic profiles at the cellular level, they lose the spatial context of cells. Over the past decade, diverse spatial transcriptomics and multi-omics technologies have been developed to analyze molecular profiles of tissue...
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Published in | Cell Systems Vol. 14; no. 10; pp. 844 - 859.e4 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
18.10.2023
Elsevier BV |
Subjects | |
Online Access | Get full text |
ISSN | 2405-4712 2405-4720 2405-4720 |
DOI | 10.1016/j.cels.2023.08.005 |
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Abstract | While single-cell sequencing technologies provide unprecedented insights into genomic profiles at the cellular level, they lose the spatial context of cells. Over the past decade, diverse spatial transcriptomics and multi-omics technologies have been developed to analyze molecular profiles of tissues. In this article, we categorize current spatial genomics technologies into three classes: optical imaging, positional indexing, and mathematical cartography. We discuss trade-offs in resolution and scale, identify limitations, and highlight synergies between existing single-cell and spatial genomics methods. Further, we propose DNA-GPS (global positioning system), a theoretical framework for large-scale optics-free spatial genomics that combines ideas from mathematical cartography and positional indexing. DNA-GPS has the potential to achieve scalable spatial genomics for multiple measurement modalities, and by eliminating the need for optical measurement, it has the potential to position cells in three-dimensions (3D).
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•Spatial transcriptomics methods exhibit trade-offs in resolution and scale•They can be split into optical imaging, positional indexing, and mathematical cartography•DNA-GPS combines ideas from positional indexing and mathematical cartography•It provides a mathematical framework for large-scale optics-free spatial transcriptomics
While single-cell sequencing methods capture genomic profiles at the cellular level, they lose spatial context. In the past decade, over a dozen spatial transcriptomics methods have been developed. Greenstreet et al. highlight trade-offs and synergies in existing methods and propose DNA-GPS, a framework for large-scale optics-free spatial transcriptomics. |
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AbstractList | While single-cell sequencing technologies provide unprecedented insights into genomic profiles at the cellular level, they lose the spatial context of cells. Over the past decade, diverse spatial transcriptomics and multi-omics technologies have been developed to analyze molecular profiles of tissues. In this article, we categorize current spatial genomics technologies into three classes: optical imaging, positional indexing, and mathematical cartography. We discuss trade-offs in resolution and scale, identify limitations, and highlight synergies between existing single-cell and spatial genomics methods. Further, we propose DNA-GPS (global positioning system), a theoretical framework for large-scale optics-free spatial genomics that combines ideas from mathematical cartography and positional indexing. DNA-GPS has the potential to achieve scalable spatial genomics for multiple measurement modalities, and by eliminating the need for optical measurement, it has the potential to position cells in three-dimensions (3D).While single-cell sequencing technologies provide unprecedented insights into genomic profiles at the cellular level, they lose the spatial context of cells. Over the past decade, diverse spatial transcriptomics and multi-omics technologies have been developed to analyze molecular profiles of tissues. In this article, we categorize current spatial genomics technologies into three classes: optical imaging, positional indexing, and mathematical cartography. We discuss trade-offs in resolution and scale, identify limitations, and highlight synergies between existing single-cell and spatial genomics methods. Further, we propose DNA-GPS (global positioning system), a theoretical framework for large-scale optics-free spatial genomics that combines ideas from mathematical cartography and positional indexing. DNA-GPS has the potential to achieve scalable spatial genomics for multiple measurement modalities, and by eliminating the need for optical measurement, it has the potential to position cells in three-dimensions (3D). While single-cell sequencing technologies provide unprecedented insights into genomic profiles at the cellular level, they lose the spatial context of cells. Over the past decade, diverse spatial transcriptomics and multi-omics technologies have been developed to analyze molecular profiles of tissues. In this article, we categorize current spatial genomics technologies into three classes: optical imaging, positional indexing, and mathematical cartography. We discuss trade-offs in resolution and scale, identify limitations, and highlight synergies between existing single-cell and spatial genomics methods. Further, we propose DNA-GPS (global positioning system), a theoretical framework for large-scale optics-free spatial genomics that combines ideas from mathematical cartography and positional indexing. DNA-GPS has the potential to achieve scalable spatial genomics for multiple measurement modalities, and by eliminating the need for optical measurement, it has the potential to position cells in three-dimensions (3D). While single-cell sequencing technologies provide unprecedented insights into genomic profiles at the cellular level, they lose the spatial context of cells. Over the past decade, diverse spatial transcriptomics and multi-omics technologies have been developed to analyze molecular profiles of tissues. In this article, we categorize current spatial genomics technologies into three classes: optical imaging, positional indexing, and mathematical cartography. We discuss trade-offs in resolution and scale, identify limitations, and highlight synergies between existing single-cell and spatial genomics methods. Further, we propose DNA-GPS (global positioning system), a theoretical framework for large-scale optics-free spatial genomics that combines ideas from mathematical cartography and positional indexing. DNA-GPS has the potential to achieve scalable spatial genomics for multiple measurement modalities, and by eliminating the need for optical measurement, it has the potential to position cells in three-dimensions (3D). [Display omitted] •Spatial transcriptomics methods exhibit trade-offs in resolution and scale•They can be split into optical imaging, positional indexing, and mathematical cartography•DNA-GPS combines ideas from positional indexing and mathematical cartography•It provides a mathematical framework for large-scale optics-free spatial transcriptomics While single-cell sequencing methods capture genomic profiles at the cellular level, they lose spatial context. In the past decade, over a dozen spatial transcriptomics methods have been developed. Greenstreet et al. highlight trade-offs and synergies in existing methods and propose DNA-GPS, a framework for large-scale optics-free spatial transcriptomics. |
Author | Heitz, Matthieu Ishiguro, Soh Greenstreet, Laura Afanassiev, Anton Kijima, Yusuke Yachie, Nozomu Schiebinger, Geoffrey King, Samuel |
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Keywords | DNA microscopy spatial transcriptomics manifold learning |
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