Abstract

Transcriptome mapping in the 3D brain RNA sequencing samples the entire transcriptome but lacks anatomical information. In situ hybridization, on the other hand, can only profile a small number of transcripts. In situ sequencing technologies address these shortcomings but face a challenge in dense, complex tissue environments. Wang et al. combined an efficient sequencing approach with hydrogel-tissue chemistry to develop a multidisciplinary technology for three-dimensional (3D) intact-tissue RNA sequencing (see the Perspective by Knöpfel). More than 1000 genes were simultaneously mapped in sections of mouse brain at single-cell resolution to define cell types and circuit states and to reveal cell organization principles. Science , this issue p. eaat5691 ; see also p. 328

Keywords

TranscriptomeComputational biologyBiologySingle cell sequencingRNAIn situ hybridizationDNA sequencingDeep sequencingIllumina dye sequencingIn situGeneGeneticsGene expressionGenomeChemistryExome sequencingPhenotype

MeSH Terms

AnimalsChromosome MappingFrontal LobeImagingThree-DimensionalMaleMiceMiceInbred C57BLMolecular ImagingNeuronsSequence AnalysisRNASingle-Cell AnalysisSomatosensory CortexTranscriptionGeneticTranscriptomeVisual Cortex

Affiliated Institutions

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Publication Info

Year
2018
Type
article
Volume
361
Issue
6400
Citations
1550
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

1550
OpenAlex
61
Influential
1365
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Cite This

Xiao Wang, William E. Allen, Matthew A. Wright et al. (2018). Three-dimensional intact-tissue sequencing of single-cell transcriptional states. Science , 361 (6400) . https://doi.org/10.1126/science.aat5691

Identifiers

DOI
10.1126/science.aat5691
PMID
29930089
PMCID
PMC6339868

Data Quality

Data completeness: 90%