Evidence map›Paper›PMID 27667365›Full record

ArticleCell systems2016

A Single-Cell Transcriptomic Map of the Human and Mouse Pancreas Reveals Inter- and Intra-cell Population Structure.

Maayan Baron, Adrian Veres, Samuel L Wolock, Aubrey L Faust, Renaud Gaujoux, Amedeo Vetere, Jennifer Hyoje Ryu, Bridget K Wagner, Shai S Shen-Orr, Allon M Klein and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell systems, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 868 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
868citing papers in PubMed, 2 pooled it
87.9field-weighted citation impact, top 1% of its field
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

868 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,729 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  11. scLGGCL: Label-Guided Graph Contrastive Learning for Single-Cell Fusion Clustering.Interdisciplinary sciences, computational life sciences · 2026
    Article
  12. Observational
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  17. Organism-scale annotation with Pan-human Azimuth.bioRxiv : the preprint server for biology · 2026
    Article
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808 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Maayan BaronFaculty of Biology, Technion - Israel Institute of Technology, Haifa 3200003, Israel.
Adrian VeresDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA; Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Samuel L WolockDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Aubrey L FaustDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
Renaud GaujouxDepartment of Immunology, Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 3200003, Israel.
Amedeo VetereCenter for the Science of Therapeutics, Broad Institute, Cambridge, MA 02142, USA.
Jennifer Hyoje RyuDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
Bridget K WagnerCenter for the Science of Therapeutics, Broad Institute, Cambridge, MA 02142, USA.
Shai S Shen-OrrDepartment of Immunology, Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 3200003, Israel.
Allon M KleinDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115, USA. Electronic address: allon_klein@hms.harvard.edu.
Douglas A MeltonDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA. Electronic address: dmelton@harvard.edu.
Itai YanaiFaculty of Biology, Technion - Israel Institute of Technology, Haifa 3200003, Israel. Electronic address: itai.yanai@nyumc.org.
Harvard University · USTechnion – Israel Institute of Technology · ILBroad Institute · USCenter for Systems Biology · US

Funding

Harvard Systems Biology Graduate ProgramT32GM080177 · NIGMS · HARVARD UNIVERSITY · PI MITCHISON, TIMOTHY J, MURRAY, ANDREW W · 2010 to 2019
$2.8M
NIGMS NIH HHS T32 GM080177
6 · The paper itself

Abstract

Although the function of the mammalian pancreas hinges on complex interactions of distinct cell types, gene expression profiles have primarily been described with bulk mixtures. Here we implemented a droplet-based, single-cell RNA-seq method to determine the transcriptomes of over 12,000 individual pancreatic cells from four human donors and two mouse strains. Cells could be divided into 15 clusters that matched previously characterized cell types: all endocrine cell types, including rare epsilon-cells; exocrine cell types; vascular cells; Schwann cells; quiescent and activated stellate cells; and four types of immune cells. We detected subpopulations of ductal cells with distinct expression profiles and validated their existence with immuno-histochemistry stains. Moreover, among human beta- cells, we detected heterogeneity in the regulation of genes relating to functional maturation and levels of ER stress. Finally, we deconvolved bulk gene expression samples using the single-cell data to detect disease-associated differential expression. Our dataset provides a resource for the discovery of novel cell type-specific transcription factors, signaling receptors, and medically relevant genes.

Indexed as

TranscriptomeAnimalsCell DifferentiationGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansIslets of LangerhansMicePancreasPancreas, ExocrineSingle-Cell AnalysisTranscription FactorsTranscription Factors

Identifiers

PMID27667365
PMCPMC5228327
OpenAlexW2523620612

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.