Evidence map›Paper›PMID 29590361›Full record

ArticleHuman molecular genetics2018

Cell type discovery using single-cell transcriptomics: implications for ontological representation.

Brian D Aevermann, Mark Novotny, Trygve Bakken, Jeremy A Miller, Alexander D Diehl, David Osumi-Sutherland, Roger S Lasken, Ed S Lein, Richard H Scheuermann

Abstract read
In one paragraph

Article in Human molecular genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A Multimodal Spatial and Epigenomic Atlas of Human Adult Lung Topography.bioRxiv : the preprint server for biology · 2025
    Article
  6. Bioconductor's Computational Ecosystem for Genomic Data Science in Cancer.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Single-cell sequencing: promises and challenges for human genetics.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2022
    Article
  13. Translational Organic Neural Interface Devices at Single Neuron Resolution.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Brian D AevermannJ. Craig Venter Institute, La Jolla, CA 92037, USA.
Mark NovotnyJ. Craig Venter Institute, La Jolla, CA 92037, USA.
Trygve BakkenAllen Institute for Brain Science, Seattle, WA 98109, USA.
Jeremy A MillerAllen Institute for Brain Science, Seattle, WA 98109, USA.
Alexander D DiehlDepartment of Biomedical Informatics, University at Buffalo, Buffalo, NY 14203, USA.
David Osumi-SutherlandEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, CB10 1SD, UK.
Roger S LaskenJ. Craig Venter Institute, La Jolla, CA 92037, USA.
Ed S LeinAllen Institute for Brain Science, Seattle, WA 98109, USA.
Richard H ScheuermannJ. Craig Venter Institute, La Jolla, CA 92037, USA.

Funding

Single-cell atlas of lung tissue-resident memory T cells reactive to upper and lower respiratory tract pathogensU19AI118626 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Pandurangan Vijayanand · 2015 to 2026
$36.7M
Somatic Mutation in the Etiology of Multiple SclerosisR21AI122100 · NIAID · J. CRAIG VENTER INSTITUTE, INC. · PI SCHEUERMANN, RICHARD H · 2016 to 2017
$552k
NIAID NIH HHS R21 AI122100NIAID NIH HHS U19 AI118626Wellcome TrustWellcome Trust 208379/Z/17/Z
6 · The paper itself

Abstract

Cells are fundamental function units of multicellular organisms, with different cell types playing distinct physiological roles in the body. The recent advent of single-cell transcriptional profiling using RNA sequencing is producing 'big data', enabling the identification of novel human cell types at an unprecedented rate. In this review, we summarize recent work characterizing cell types in the human central nervous and immune systems using single-cell and single-nuclei RNA sequencing, and discuss the implications that these discoveries are having on the representation of cell types in the reference Cell Ontology (CL). We propose a method, based on random forest machine learning, for identifying sets of necessary and sufficient marker genes, which can be used to assemble consistent and reproducible cell type definitions for incorporation into the CL. The representation of defined cell type classes and their relationships in the CL using this strategy will make the cell type classes being identified by high-throughput/high-content technologies findable, accessible, interoperable and reusable (FAIR), allowing the CL to serve as a reference knowledgebase of information about the role that distinct cellular phenotypes play in human health and disease.

Indexed as

Big DataCell LineageGene Expression ProfilingHumansSequence Analysis, RNASingle-Cell AnalysisTranscriptome

Identifiers

PMID29590361
PMCPMC5946857

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.