Evidence map›Paper›PMID 40290316›Full record

ArticleNAR genomics and bioinformatics2025

ARTdeConv: adaptive regularized tri-factor non-negative matrix factorization for cell type deconvolution.

Tianyi Liu, Chuwen Liu, Quefeng Li, Xiaojing Zheng, Fei Zou

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. 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

5 · Who and what money

Authors and funding

5 authors.

Tianyi LiuDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID https://orcid.org/0000-0002-2484-2478
Chuwen LiuDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.
Quefeng LiDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID https://orcid.org/0000-0003-0707-2763
Xiaojing ZhengDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.ORCID https://orcid.org/0000-0003-2248-933X
Fei ZouDepartment of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.

Funding

University of North Carolina - Chlamydia Vaccine Initiative (UNC-CVI)U19AI144181 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI O'CONNELL, CATHERINE MARY · 2019 to 2023
$10.7M
Natural History of Chlamydia trachomatis genital tract infection in womenR01AI170959 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Toni Darville, CATHERINE MARY O'CONNELL · 2024 to 2026
$2.2M
Statistical Methods for Integrative Analysis of Large Scale Neuroimaging DataR01AG073259 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, QUEFENG · 2021 to 2025
$1.8M
Enhanced Machine Learning Tools for Complex Data Evaluation and Integration in Advancing Health OutcomesR01HL173044 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Baiming Zou, Fei Zou · 2025 to 2026
$1.3M
NHLBI NIH HHS R01 HL173044NIAID NIH HHS R01 AI170959NIAID NIH HHS U19 AI144181NIA NIH HHS R01 AG073259
6 · The paper itself

Abstract

Accurate deconvolution of cell types from bulk gene expression is crucial for understanding cellular compositions and uncovering cell-type specific differential expression and physiological states of diseased tissues. Existing deconvolution methods have limitations, such as requiring complete cellular gene expression signatures or neglecting partial biological information. Moreover, these methods often overlook varying cell-type messenger RNA amounts, leading to biased proportion estimates. Additionally, they do not effectively utilize valuable reference information from external studies, such as means and ranges of population cell-type proportions. To address these challenges, we introduce an adaptive regularized tri-factor non-negative matrix factorization approach for deconvolution (ARTdeConv). We rigorously establish the numerical convergence of our algorithm. Through benchmark simulations, we demonstrate the superior performance of ARTdeConv compared to state-of-the-art semi-reference-based and reference-free methods as well as its robustness under challenges to its assumptions. In a real-world application to a dataset from a trivalent influenza vaccine study, our method accurately estimates cellular proportions, as evidenced by the nearly perfect Pearson's correlation between ARTdeConv estimates and flow cytometry measurements. Moreover, our analysis of ARTdeConv estimates in COVID-19 patients reveals patterns consistent with important immunological phenomena observed in other studies. The proposed method, ARTdeConv, is implemented as an R package and can be accessed on GitHub for researchers and practitioners.

Indexed as

AlgorithmsGene Expression ProfilingCOVID-19HumansInfluenza VaccinesSARS-CoV-2Influenza Vaccines

Identifiers

PMID40290316
PMCPMC12034106

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.