Evidence map›Paper›PMID 39313646›Full record

ArticleNature biotechnology2025

Coordinated, multicellular patterns of transcriptional variation that stratify patient cohorts are revealed by tensor decomposition.

Jonathan Mitchel, M Grace Gordon, Richard K Perez, Evan Biederstedt, Raymund Bueno, Chun Jimmie Ye, Peter V Kharchenko

Abstract read
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Article in Nature biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. iScience · 2026
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  14. PULSAR: a Foundation Model for Multi-scale and Multi-cellular Biology.bioRxiv : the preprint server for biology · 2025
    Article
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  16. Article
  17. Review
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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

7 authors.

Jonathan MitchelDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6026-2278
M Grace GordonInstitute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA.
Richard K PerezSchool of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Evan BiederstedtDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Raymund BuenoInstitute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA.
Chun Jimmie YeInstitute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA. jimmie.ye@ucsf.edu.ORCID http://orcid.org/0000-0001-6560-3783
Peter V KharchenkoDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. pkharchenko@altoslabs.com.ORCID http://orcid.org/0000-0002-6036-5875

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue-level and organism-level biological processes often involve the coordinated action of multiple distinct cell types. The recent application of single-cell assays to many individuals should enable the study of how donor-level variation in one cell type is linked to that in other cell types. Here we introduce a computational approach called single-cell interpretable tensor decomposition (scITD) to identify common axes of interindividual variation by considering joint expression variation across multiple cell types. scITD combines expression matrices from each cell type into a higher-order matrix and factorizes the result using the Tucker tensor decomposition. Applying scITD to single-cell RNA-sequencing data on 115 persons with lupus and 83 persons with coronavirus disease 2019, we identify patterns of coordinated cellular activity linked to disease severity and specific phenotypes, such as lupus nephritis. scITD results also implicate specific signaling pathways likely mediating coordination between cell types. Overall, scITD offers a tool for understanding the covariation of cell states across individuals, which can yield insights into the complex processes that define and stratify disease.

Indexed as

COVID-19Single-Cell AnalysisCohort StudiesGene Expression ProfilingHumansLupus Erythematosus, SystemicLupus NephritisSARS-CoV-2Sequence Analysis, RNATranscriptome

Identifiers

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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.