Evidence map›Paper›PMID 32103204›Full record

ArticleNature protocols2020

CellPhoneDB: inferring cell-cell communication from combined expression of multi-subunit ligand-receptor complexes.

Mirjana Efremova, Miquel Vento-Tormo, Sarah A Teichmann, Roser Vento-Tormo

Abstract read
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In one paragraph

Article in Nature protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2,160 papers.

0numbers the graph read from it
0cells of the map it votes in
2,160citing papers in PubMed
174.4field-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

2,160 citing papers in PubMed, 3,514 citations in OpenAlex.

  1. Trial
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2,100 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

4 authors at 3 institutions in 2 countries.

Mirjana EfremovaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Miquel Vento-TormoYDEVS Software Development, Valencia, Spain.
Sarah A TeichmannWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-6294-6366
Roser Vento-TormoWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK. rv4@sanger.ac.uk.ORCID http://orcid.org/0000-0002-9870-8474
Wellcome Sanger Institute · GBSoftware (Spain) · ESUniversity of Cambridge · GB

Funding

Wellcome Trust (Wellcome) 211276/Z/18/ZWellcome Trust (Wellcome) WT206194
6 · The paper itself

Abstract

Cell-cell communication mediated by ligand-receptor complexes is critical to coordinating diverse biological processes, such as development, differentiation and inflammation. To investigate how the context-dependent crosstalk of different cell types enables physiological processes to proceed, we developed CellPhoneDB, a novel repository of ligands, receptors and their interactions. In contrast to other repositories, our database takes into account the subunit architecture of both ligands and receptors, representing heteromeric complexes accurately. We integrated our resource with a statistical framework that predicts enriched cellular interactions between two cell types from single-cell transcriptomics data. Here, we outline the structure and content of our repository, provide procedures for inferring cell-cell communication networks from single-cell RNA sequencing data and present a practical step-by-step guide to help implement the protocol. CellPhoneDB v.2.0 is an updated version of our resource that incorporates additional functionalities to enable users to introduce new interacting molecules and reduces the time and resources needed to interrogate large datasets. CellPhoneDB v.2.0 is publicly available, both as code and as a user-friendly web interface; it can be used by both experts and researchers with little experience in computational genomics. In our protocol, we demonstrate how to evaluate meaningful biological interactions with CellPhoneDB v.2.0 using published datasets. This protocol typically takes ~2 h to complete, from installation to statistical analysis and visualization, for a dataset of ~10 GB, 10,000 cells and 19 cell types, and using five threads.

Indexed as

SoftwareAnimalsCell CommunicationGene Expression ProfilingHumansLigandsMiceReceptors, Cell SurfaceSequence Analysis, RNASignal TransductionSingle-Cell AnalysisTranscriptomeLigandsReceptors, Cell Surface

Identifiers

PMID32103204
OpenAlexW3007935255

What OpenQuestion holds

Textmetadata
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.