Evidence map›Paper›PMID 42039615›Full record

ArticlebioRxiv : the preprint server for biology2026

Tracing cell communication programs across conditions at single cell resolution with CCC-RISE.

Andrew Ramirez, Nathaniel Thomas, Daniel R Calabrese, John R Greenland, Aaron S Meyer

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Andrew RamirezDepartment of Bioengineering, University of California, Los Angeles (UCLA), Los Angeles, CA 90095, USA.
Nathaniel ThomasDepartment of Computer Science, UCLA, Los Angeles, CA 90095, USA.
Daniel R CalabreseDepartment of Medicine, University of California, San Francisco (UCSF), San Francisco, CA 94143, USA.
John R GreenlandDepartment of Medicine, University of California, San Francisco (UCSF), San Francisco, CA 94143, USA.
Aaron S MeyerDepartment of Bioengineering, University of California, Los Angeles (UCLA), Los Angeles, CA 90095, USA.ORCID 0000-0003-4513-1840

Funding

Systems Epigenomics of Persistent Bloodstream InfectionU19AI172713 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI Michael R Yeaman · 2023 to 2026
$11.6M
NIAID NIH HHS U19 AI172713
6 · The paper itself

Abstract

Cell-cell communication (CCC) mediates coordinated cellular activities that vary dynamically across time, location, and biological context. While various tools exist to infer CCC, they typically aggregate data according to pre-defined cell types, obscuring critical single-cell heterogeneity. Furthermore, because signaling pathways and cell populations operate in a coordinated manner, an integrative analytical approach is essential. To address these challenges, we developed CCC-RISE, an extension of the tensor-based method Reduction and Insight in Single-cell Exploration (RISE). CCC-RISE identifies integrative patterns of single-cell variation by deconvolving communication into interpretable modules defined by unique sender cells, receiver cells, ligands, and condition associations. We applied this framework to a COVID-19 cohort with varying disease severity and a lung transplant cohort with acute allograft dysfunction. In both contexts, CCC-RISE successfully identified disease-relevant communication programs and traced them to specific cellular subpopulations, often crossing conventional cell-type boundaries. This approach offers a robust pipeline enabling the identification of disease-relevant signaling subpopulations that are invisible to aggregate methods.

Indexed as

cell-cell communicationligand-receptor interactionsmulti-conditionPARAFAC2Research reportscRNA-seqtensor decomposition

Identifiers

PMID42039615
PMCPMC13105001

What Socratic holds

Textmetadata
LicenceCC BY-ND
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 Socratic graph.