Evidence map›Paper›PMID 37144485›Full record

ArticleNucleic acids research2023

Inferring ligand-receptor cellular networks from bulk and spatial transcriptomic datasets with BulkSignalR.

Jean-Philippe Villemin, Laia Bassaganyas, Didier Pourquier, Florence Boissière, Simon Cabello-Aguilar, Evelyne Crapez, Rita Tanos, Emmanuel Cornillot, Andrei Turtoi, Jacques Colinge

Abstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Dynamic Remodeling of Oocyte-Granulosa Cell Communication During Bovine Folliculogenesis Revealed by Transcriptomic Meta-Analyses.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Pooled it
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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

10 authors.

Jean-Philippe VilleminInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.ORCID 0000-0002-1838-5880
Laia BassaganyasInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.
Didier PourquierInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.
Florence BoissièreInstitut régional du Cancer Montpellier (ICM), Montpellier, France.
Simon Cabello-AguilarInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.
Evelyne CrapezInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.
Rita TanosInstitut régional du Cancer Montpellier (ICM), Montpellier, France.
Emmanuel CornillotInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.ORCID 0000-0002-1202-1162
Andrei TurtoiInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.
Jacques ColingeInstitut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U 1194, Montpellier, France.

Funding

European UnionFondation ARC pour la Recherche sur le Cancer PJA 20141201975J.C. INCa R17080FF-CTRégion Occitanie, programme Recherche et Société(s)
6 · The paper itself

Abstract

The study of cellular networks mediated by ligand-receptor interactions has attracted much attention recently owing to single-cell omics. However, rich collections of bulk data accompanied with clinical information exists and continue to be generated with no equivalent in single-cell so far. In parallel, spatial transcriptomic (ST) analyses represent a revolutionary tool in biology. A large number of ST projects rely on multicellular resolution, for instance the Visium™ platform, where several cells are analyzed at each location, thus producing localized bulk data. Here, we describe BulkSignalR, a R package to infer ligand-receptor networks from bulk data. BulkSignalR integrates ligand-receptor interactions with downstream pathways to estimate statistical significance. A range of visualization methods complement the statistics, including functions dedicated to spatial data. We demonstrate BulkSignalR relevance using different datasets, including new Visium liver metastasis ST data, with experimental validation of protein colocalization. A comparison with other ST packages shows the significantly higher quality of BulkSignalR inferences. BulkSignalR can be applied to any species thanks to its built-in generic ortholog mapping functionality.

Identifiers

PMID37144485
PMCPMC10250239

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LicenceCC BY-NC
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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.