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Transcriptome-wide spatial RNA profiling maps the cellular architecture of the developing human neocortex

View ORCID ProfileKenny Roberts, Alexander Aivazidis, View ORCID ProfileVitalii Kleshchevnikov, Tong Li, Robin Fropf, Michael Rhodes, View ORCID ProfileJoseph M. Beechem, View ORCID ProfileMartin Hemberg, View ORCID ProfileOmer Ali Bayraktar
doi: https://doi.org/10.1101/2021.03.20.436265
Kenny Roberts
1Wellcome Sanger Institute, Cambridge, CB10 1SA, UK
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Alexander Aivazidis
1Wellcome Sanger Institute, Cambridge, CB10 1SA, UK
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Vitalii Kleshchevnikov
1Wellcome Sanger Institute, Cambridge, CB10 1SA, UK
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Tong Li
1Wellcome Sanger Institute, Cambridge, CB10 1SA, UK
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Robin Fropf
2NanoString Technologies Inc., 530 Fairview Avenue North, Seattle, WA 98109, USA
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Michael Rhodes
2NanoString Technologies Inc., 530 Fairview Avenue North, Seattle, WA 98109, USA
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Joseph M. Beechem
2NanoString Technologies Inc., 530 Fairview Avenue North, Seattle, WA 98109, USA
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Martin Hemberg
1Wellcome Sanger Institute, Cambridge, CB10 1SA, UK
3Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women’s Hospital, Boston, MA
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Omer Ali Bayraktar
1Wellcome Sanger Institute, Cambridge, CB10 1SA, UK
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  • ORCID record for Omer Ali Bayraktar
  • For correspondence: ob5@sanger.ac.uk
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Abstract

Spatial genomic technologies can map gene expression in tissues, but provide limited potential for transcriptome-wide discovery approaches and application to fixed tissue samples. Here, we introduce the GeoMX Whole Transcriptome Atlas (WTA), a new technology for transcriptome-wide spatial profiling of tissues with cellular resolution. WTA significantly expands the Digital Spatial Profiling approach to enable in situ hybridisation against 18,190 genes at high-throughput using a sequencing readout. We applied WTA to generate the first spatial transcriptomic map of the fetal human neocortex, validating transcriptome-wide spatial profiling on formalin-fixed tissue material and demonstrating the spatial enrichment of autism gene expression in deep cortical layers. To demonstrate the value of WTA for cell atlasing, we integrated single-cell RNA-sequencing (scRNA-seq) and WTA data to spatially map dozens of neural cell types and showed that WTA can be used to directly measure cell type specific transcriptomes in situ. Moreover, we developed computational tools for background correction of WTA data and accurate integration with scRNA-seq. Our results present WTA as a versatile transcriptome-wide discovery tool for cell atlasing and fixed tissue spatial transcriptomics.

Competing Interest Statement

Robin Fropf, Michael Rhodes, and Joseph M. Beechem are employees of NanoString Technologies, Inc.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted March 20, 2021.
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Transcriptome-wide spatial RNA profiling maps the cellular architecture of the developing human neocortex
Kenny Roberts, Alexander Aivazidis, Vitalii Kleshchevnikov, Tong Li, Robin Fropf, Michael Rhodes, Joseph M. Beechem, Martin Hemberg, Omer Ali Bayraktar
bioRxiv 2021.03.20.436265; doi: https://doi.org/10.1101/2021.03.20.436265
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Transcriptome-wide spatial RNA profiling maps the cellular architecture of the developing human neocortex
Kenny Roberts, Alexander Aivazidis, Vitalii Kleshchevnikov, Tong Li, Robin Fropf, Michael Rhodes, Joseph M. Beechem, Martin Hemberg, Omer Ali Bayraktar
bioRxiv 2021.03.20.436265; doi: https://doi.org/10.1101/2021.03.20.436265

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