{
  "abstract": "Imaging-based spatially resolved transcriptomics (imSRT) technologies provide high-throughput molecular-resolution spatial characterization of genes within cells. Conventional analysis methods to identify cell-types and states in imSRT data rely on gene count matrices derived from tallying the number of mRNA molecules detected for each gene per segmented cell, thereby overlooking subcellular heterogeneity that can be useful in defining cell states. To take advantage of the molecular-resolution information in imSRT data and potentially identify cell-states based on subcellular heterogeneity, we developed STARIT (Spatial Transcriptomics As Rasterized Image Tensors). STARIT converts transcripts within segmented cells in imSRT data into an image-based tensor representation that can be combined with deep learning computer vision models for downstream analysis. Using simulated and real imSRT data, we demonstrate that STARIT distinguishes transcriptionally distinct cell-types and further separates cell states based on subcellular transcript localization, which conventional gene count analysis fails to capture. By providing a standardized framework to encode subcellular molecular information in imSRT data, STARIT will enable deeper insights into subcellular heterogeneity and enhance the identification and characterization of cell-types and states that are overlooked by gene count representations. Author summary: Imaging-based spatial transcriptomics technologies can map the locations of individual RNA transcripts within cells, providing an opportunity to study how genes are spatially organized at subcellular resolution. However, most current analysis approaches simplify these data by counting transcripts per cell, reducing rich spatial information into cell-by-gene matrices and potentially overlooking biologically meaningful differences in subcellular transcript organization.",
  "abstract_shown": true,
  "affiliations": [
    "Center for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.",
    "Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America."
  ],
  "article_type": "Research Article",
  "arxiv": null,
  "author_total": 5,
  "authors": [
    {
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        0,
        1
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      "name": "Dee Velazquez"
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    {
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        0,
        1
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      "name": "Caleb Hallinan"
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    {
      "affs": [
        0,
        1
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      "name": "Roujin An"
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    {
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        0,
        1
      ],
      "name": "Kalen Clifton",
      "orcid": "0000-0002-4095-8104"
    },
    {
      "affs": [
        0,
        1
      ],
      "name": "Jean Fan",
      "orcid": "0000-0002-0212-5451"
    }
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  "bibtex": "https://research.draconitic.com/paper/6j45e352nt6db.bib",
  "cited_by": 0,
  "doi": "10.1371/journal.pcbi.1014845",
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  "native_subjects": [
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  "pmcid": "PMC13657327",
  "pmid": "42837397",
  "published": "2026-10-06",
  "publisher": "Public Library of Science",
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  "subjects": [
    {
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      "subfield": "bioinformatics"
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      "origin": "plos:genetics",
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    {
      "field": "mathematics",
      "origin": "plos:statistical methods",
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  "title": "Spatial Transcriptomics As Rasterized Image Tensors (STARIT) characterizes cell states with subcellular molecular heterogeneity",
  "title_text": "Spatial Transcriptomics As Rasterized Image Tensors (STARIT) characterizes cell states with subcellular molecular heterogeneity",
  "type": "peer-reviewed",
  "updated_at": "2026-10-30T12:18:03Z",
  "url": "https://research.draconitic.com/paper/6j45e352nt6db",
  "venue": "PLOS Computational Biology",
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