Abstract

Spatial localization is a key determinant of cellular fate and behavior, but methods for spatially resolved, transcriptome-wide gene expression profiling across complex tissues are lacking. RNA staining methods assay only a small number of transcripts, whereas single-cell RNA-seq, which measures global gene expression, separates cells from their native spatial context. Here we present Seurat, a computational strategy to infer cellular localization by integrating single-cell RNA-seq data with in situ RNA patterns. We applied Seurat to spatially map 851 single cells from dissociated zebrafish (Danio rerio) embryos and generated a transcriptome-wide map of spatial patterning. We confirmed Seurat's accuracy using several experimental approaches, then used the strategy to identify a set of archetypal expression patterns and spatial markers. Seurat correctly localizes rare subpopulations, accurately mapping both spatially restricted and scattered groups. Seurat will be applicable to mapping cellular localization within complex patterned tissues in diverse systems.

Keywords

Computational biologyGene expressionGeneBiologyGenetics

MeSH Terms

AnimalsGene Expression RegulationDevelopmentalHigh-Throughput Nucleotide SequencingImage ProcessingComputer-AssistedIn Situ HybridizationFluorescenceSingle-Cell AnalysisTranscriptomeZebrafish

Affiliated Institutions

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Publication Info

Year
2015
Type
article
Volume
33
Issue
5
Pages
495-502
Citations
6934
Access
Closed

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6934
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632
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Cite This

Rahul Satija, Jeffrey A. Farrell, David Gennert et al. (2015). Spatial reconstruction of single-cell gene expression data. Nature Biotechnology , 33 (5) , 495-502. https://doi.org/10.1038/nbt.3192

Identifiers

DOI
10.1038/nbt.3192
PMID
25867923
PMCID
PMC4430369

Data Quality

Data completeness: 86%