Evidence map›Paper›PMID 25867922›Full record

ArticleNature biotechnology2015

High-throughput spatial mapping of single-cell RNA-seq data to tissue of origin.

Kaia Achim, Jean-Baptiste Pettit, Luis R Saraiva, Daria Gavriouchkina, Tomas Larsson, Detlev Arendt, John C Marioni

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biotechnology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 222 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
222citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

222 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Spatial coherence in DNA barcode networks.Patterns (New York, N.Y.) · 2025
    Article
  8. Article
  9. Article
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  11. Spatial transcriptomic applications in orthopedics.Connective tissue research · 2025
    Review
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162 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Kaia Achim1] European Bioinformatics Institute, European Molecular Biology Laboratory (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK. [2] Developmental Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID 0000000337234065
Jean-Baptiste PettitEuropean Bioinformatics Institute, European Molecular Biology Laboratory (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK.
Luis R Saraiva1] European Bioinformatics Institute, European Molecular Biology Laboratory (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK. [2] Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK.ORCID 0000000340790396
Daria GavriouchkinaDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Tomas LarssonDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Detlev ArendtDevelopmental Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
John C Marioni1] European Bioinformatics Institute, European Molecular Biology Laboratory (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK. [2] Developmental Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany. [3] Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Understanding cell type identity in a multicellular organism requires the integration of gene expression profiles from individual cells with their spatial location in a particular tissue. Current technologies allow whole-transcriptome sequencing of spatially identified cells but lack the throughput needed to characterize complex tissues. Here we present a high-throughput method to identify the spatial origin of cells assayed by single-cell RNA-sequencing within a tissue of interest. Our approach is based on comparing complete, specificity-weighted mRNA profiles of a cell with positional gene expression profiles derived from a gene expression atlas. We show that this method allocates cells to precise locations in the brain of the marine annelid Platynereis dumerilii with a success rate of 81%. Our method is applicable to any system that has a reference gene expression database of sufficiently high resolution.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsHigh-Throughput Nucleotide SequencingOrgan SpecificityPolychaetaSingle-Cell AnalysisTranscriptome

Identifiers

PMID25867922

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.