Evidence map›Paper›PMID 27824854›Full record

ReviewNature biotechnology2016

Revealing the vectors of cellular identity with single-cell genomics.

Allon Wagner, Aviv Regev, Nir Yosef

Registry-linked trialAbstract readReview
In one paragraph

Review in Nature biotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05209061 (Cellular Composition of the Human Appendix Using Single-cell RNA and Single-cell ATAC-sequencing.), which is not on this map. Cited by 366 papers.

0numbers the graph read from it
0cells of the map it votes in
366citing 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.

NCT05209061 completednot on this mapstarted 2023, after this paper: background citation

Cellular Composition of the Human Appendix Using Single-cell RNA and Single-cell ATAC-sequencing.

Typeobservational_patient_registrySponsorBispebjerg HospitalRan2023 to 2026Enrolled5ConditionsDiabetes, Appendicitis, Inflammatory Bowel DiseasesArmsBiopsy
3 · Its place in the literature

Who cites it

366 citing papers in PubMed.

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  11. Review
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  13. Computational modelling of cell identity.The Biochemical journal · 2026
    Review
  14. Article
  15. Article
  16. Article
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306 more citing papers are in PubMed but not listed here.

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

3 authors.

Allon WagnerDepartment of Electrical Engineering and Computer Science and the Center for Computational Biology, University of California, Berkeley, California, USA.
Aviv RegevHoward Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Nir YosefDepartment of Electrical Engineering and Computer Science and the Center for Computational Biology, University of California, Berkeley, California, USA.

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
Center for Cell CircuitsP50HG006193 · NHGRI · BROAD INSTITUTE, INC. · PI REGEV, AVIV · 2011 to 2015
$15.6M
Center for Cell CircuitsRM1HG006193 · NHGRI · BROAD INSTITUTE, INC. · PI BLAINEY, PAUL CLARK, HACOHEN, NIR · 2016 to 2020
$14.9M
Trinity: Transcriptome assembly for genetic and functional analysis of cancerU24CA180922 · NCI · BROAD INSTITUTE, INC. · PI HAAS, BRIAN · 2013 to 2022
$7.5M
Classification of Cortical Neurons by Single Cell TranscriptomicsU01MH105979 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI NGAI, JOHN J. · 2014 to 2016
$4.5M
Comprehensive Classification Of Neuronal Subtypes By Single Cell TranscriptomicsU01MH105960 · NIMH · HARVARD UNIVERSITY · PI REGEV, AVIV, SANES, JOSHUA R · 2014 to 2016
$4.5M
An integrated multiplexed genomic assay for low input clinical samples1U24AI118672 · NIAID · BROAD INSTITUTE, INC. · PI SHALEK, ALEX K · 2015 to 2019
$2.0M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA014051NCI NIH HHS U24 CA180922NHGRI NIH HHS P50 HG006193NHGRI NIH HHS RM1 HG006193NIAID NIH HHS U24 AI118672NIMH NIH HHS U01 MH105960NIMH NIH HHS U01 MH105979
6 · The paper itself

Abstract

Single-cell genomics has now made it possible to create a comprehensive atlas of human cells. At the same time, it has reopened definitions of a cell's identity and of the ways in which identity is regulated by the cell's molecular circuitry. Emerging computational analysis methods, especially in single-cell RNA sequencing (scRNA-seq), have already begun to reveal, in a data-driven way, the diverse simultaneous facets of a cell's identity, from discrete cell types to continuous dynamic transitions and spatial locations. These developments will eventually allow a cell to be represented as a superposition of 'basis vectors', each determining a different (but possibly dependent) aspect of cellular organization and function. However, computational methods must also overcome considerable challenges-from handling technical noise and data scale to forming new abstractions of biology. As the scale of single-cell experiments continues to increase, new computational approaches will be essential for constructing and characterizing a reference map of cell identities.

Indexed as

AnimalsCell Physiological PhenomenaComputer SimulationGene Expression ProfilingGene Expression RegulationHigh-Throughput Nucleotide SequencingHumansModels, BiologicalProteomeSignal TransductionTranscriptomeProteome

Identifiers

PMID27824854
PMCPMC5465644

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Registered trials

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.