Evidence map›Paper›PMID 40985689›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

CellPhenoX: An Explainable Machine Learning Method for Identifying Cell Phenotypes To Predict Clinical Outcomes from Single-Cell Multi-Omics.

Jade Young, Jun Inamo, Zachary Caterer, Revanth Krishna, Fan Zhang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Microbiome-Driven Risk Stratification and Biotherapeutics in Radiation Enteritis.Computational and structural biotechnology journal · 2026
    Review
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Jade YoungDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, CO, USA.ORCID https://orcid.org/0000-0003-0887-3319
Jun InamoDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, CO, USA.
Zachary CatererInterdisciplinary Quantitative Biology PhD Program, BioFrontiers Institute, University of Colorado, Boulder, CO, USA.
Revanth KrishnaDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, CO, USA.
Fan ZhangDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, CO, USA.ORCID https://orcid.org/0000-0002-6102-2970

Funding

Computational Bioscience Program Training GrantT15LM009451 · NLM · UNIVERSITY OF COLORADO DENVER · PI Katherina Kechris-Mays, Arjun Krishnan · 2007 to 2026
$11.7M
Deciphering Complement-Dependent Macrophage Phenotypes in Human Autoimmune ArthritisR01AR085156 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI FAN ZHANG · 2025 to 2026
$766k
Accelerating Medicines Partnership-Autoimmune and Immunologic Diseases Leadership Scholar Program 5UCAR081032-04NIAMS NIH HHS R01 AR085156NIAMS NIH HHS R01AR085156NLM NIH HHS T15 LM009451U.S. National Library of Medicine
6 · The paper itself

Abstract

Single-cell technologies have transformed the understanding of disease heterogeneity, but linking cell-level phenotypic alterations to clinical outcomes becomes increasingly challenging as single-cell datasets continue to expand. This is further complicated by the lack of interpretability in existing methods and the difficulty of detecting interaction effects-nonlinear dependencies between factors like sex, age, and disease. To address this, a novel explainable machine learning method, CellPhenoX, is developed to identify cell-specific phenotypes and interaction effects linked to clinical outcomes. CellPhenoX integrates classification models, explainable artificial intelligence (AI) techniques, and a statistical framework to generate interpretable, cell-specific scores to uncover condition-associated cell populations. Extensive benchmarking and applications demonstrate the efficacy of CellPhenoX across diverse single-cell study designs, including the dedicated and disease-motivated simulations, binary disease-control comparisons, and severity-stratified patient cohorts. Notably, CellPhenoX identifies an activated monocyte phenotype in COVID-19, with expansion correlated with disease severity after adjusting for covariates and interactive effects. It also uncovers a fibroblast-specific state transition gradient predicting tissue inflammation in chronic diseases, and identifies therapy-induced T cell changes and biomarkers linked to the tumor microenvironment. By integrating interpretability into clinical classification, CellPhenoX offers a powerful framework for translating single-cell findings into clinical impact.

Indexed as

COVID-19Machine LearningSingle-Cell AnalysisHumansMultiomicsPhenotypeSARS-CoV-2clinical associationdifferential abundanceexplainable machine learningSingle‐cell multi‐omics

Identifiers

PMID40985689
PMCPMC12622556

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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.