Evidence map›Paper›PMID 40585304›Full record

ArticleNAR genomics and bioinformatics2025

Differential cellular communication inference framework for large-scale single-cell RNA-sequencing data.

Giulia Cesaro, Giacomo Baruzzo, Gaia Tussardi, Barbara Di Camillo

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. iScience · 2026
    Article
  2. Article
  3. bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

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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.

Giulia CesaroDepartment of Information Engineering, University of Padova, Padova 35131, Italy.ORCID https://orcid.org/0000-0001-7971-963X
Giacomo BaruzzoDepartment of Information Engineering, University of Padova, Padova 35131, Italy.ORCID https://orcid.org/0000-0001-6129-5007
Gaia TussardiDepartment of Information Engineering, University of Padova, Padova 35131, Italy.ORCID https://orcid.org/0009-0009-7173-2683
Barbara Di CamilloDepartment of Information Engineering, University of Padova, Padova 35131, Italy.ORCID https://orcid.org/0000-0001-8415-4688

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell transcriptomics data have been widely used to characterize biological systems, particularly in studying cell-cell communication, which plays a significant role in many biological processes. Despite the availability of various computational tools for inferring cellular communication, quantifying variations across different experimental conditions at both intercellular and intracellular levels remains challenging. Moreover, available methods are in general limited in terms of flexibility in analyzing different experimental designs and the ability to visualize results in an easily interpretable way. Here, we present a generalizable computational framework designed to infer and support differential cellular communication analysis across two experimental conditions from large-scale single-cell transcriptomics data. The scSeqCommDiff tool employs a statistical and network-based computational approach for characterizing altered cellular cross-talk in a fast and memory-efficient way. The framework is complemented with CClens, a user-friendly Shiny app to facilitate interactive analysis of inferred cell-cell communication. Validation through spatial transcriptomics data, comparison with other tools, and application to large-scale datasets (including a cell atlas) confirms the reliability, scalability, and efficiency of the framework. Moreover, the application to a single-nucleus transcriptomics dataset shows the validity and ability of the proposed workflow to support and unravel alterations in cell-cell interactions among patients with amyotrophic lateral sclerosis and healthy subjects.

Indexed as

Cell CommunicationSequence Analysis, RNASingle-Cell AnalysisSoftwareTranscriptomeComputational BiologyGene Expression ProfilingHumans

Identifiers

PMID40585304
PMCPMC12204404

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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.