Evidence map›Paper›PMID 32759341›Full record

ArticleGenome research2020

A limited set of transcriptional programs define major cell types.

Alessandra Breschi, Manuel Muñoz-Aguirre, Valentin Wucher, Carrie A Davis, Diego Garrido-Martín, Sarah Djebali, Jesse Gillis, Dmitri D Pervouchine, Anna Vlasova, Alexander Dobin and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  13. Molecular Landscape of Tourette's Disorder.International journal of molecular sciences · 2023
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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

18 authors at 7 institutions in 5 countries.

Alessandra Breschi *Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Manuel Muñoz-Aguirre *Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Valentin Wucher *Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Carrie A DavisCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Diego Garrido-MartínCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Sarah DjebaliCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Jesse GillisDepartment of Genetics, Stanford University, Stanford, California 94305, USA.
Dmitri D PervouchineCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Anna VlasovaResearch Institute of Molecular Pathology (IMP), Vienna Biocenter (VBC), 1030 Vienna, Austria.
Alexander DobinCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Chris ZaleskiCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Jorg DrenkowCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Cassidy DanykoCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Alexandra ScavelliCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Ferran ReverterCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Michael P SnyderDepartment of Genetics, Stanford University, Stanford, California 94305, USA.
Thomas R GingerasCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11742, USA.
Roderic GuigóCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, E-08003 Barcelona, Catalonia, Spain.
Cold Spring Harbor Laboratory · USUniversitat Pompeu Fabra · ESBarcelona Institute of Science and Technology · ESStanford University · USResearch Institute of Molecular Pathology · ATSkolkovo Institute of Science and Technology · RUUniversité Toulouse III - Paul Sabatier · FR

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
GENCODE Resource ProjectU41HG007234 · NHGRI · SANGER INSTITUTE · PI FLICEK, PAUL · 2013 to 2020
$20.3M
Landscape of transcription in human and mouseU54HG007004 · NHGRI · COLD SPRING HARBOR LABORATORY · PI GINGERAS, THOMAS RAYMOND · 2012 to 2017
$10.6M
Methods for high-resolution analysis of genetic effects on gene expressionR01MH101814 · NIMH · UNIVERSITY OF GENEVA · PI BUSTAMANTE, CARLOS DANIEL, DERMITZAKIS, EMMANOUIL · 2013 to 2016
$2.3M
NCI NIH HHS P30 CA045508NHGRI NIH HHS U41 HG007234NHGRI NIH HHS U54 HG007004NIMH NIH HHS R01 MH101814
6 · The paper itself

Abstract

We have produced RNA sequencing data for 53 primary cells from different locations in the human body. The clustering of these primary cells reveals that most cells in the human body share a few broad transcriptional programs, which define five major cell types: epithelial, endothelial, mesenchymal, neural, and blood cells. These act as basic components of many tissues and organs. Based on gene expression, these cell types redefine the basic histological types by which tissues have been traditionally classified. We identified genes whose expression is specific to these cell types, and from these genes, we estimated the contribution of the major cell types to the composition of human tissues. We found this cellular composition to be a characteristic signature of tissues and to reflect tissue morphological heterogeneity and histology. We identified changes in cellular composition in different tissues associated with age and sex, and found that departures from the normal cellular composition correlate with histological phenotypes associated with disease.

Indexed as

Transcription, GeneticCell LineEndothelial CellsEpithelial CellsFemaleGene Expression ProfilingGynecomastiaHumansMaleMesodermNeoplasmsOrgan SpecificitySequence Analysis, RNA

Identifiers

PMID32759341
PMCPMC7397875
OpenAlexW3046627240

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.