Evidence map›Paper›PMID 41112940›Full record

ArticleJournal of data science : JDS2025

EMixed: Probabilistic Multi-Omics Cellular Deconvolution of Bulk Omics Data.

Manqi Cai, Kangyi Zhao, Penghui Huang, Juan C Celedón, Chris McKennan, Wei Chen, Jiebiao Wang

Abstract read
In one paragraph

Article in Journal of data science : JDS, 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

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.

Manqi CaiDepartment of Biostatistics and Health Data Science, University of Pittsburgh, USA.
Kangyi ZhaoDepartment of Statistics, University of Pittsburgh, USA.
Penghui HuangDepartment of Biostatistics and Health Data Science, University of Pittsburgh, USA.
Juan C CeledónDepartment of Pediatrics, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, USA.
Chris McKennanDepartment of Statistics, University of Pittsburgh, USA.
Wei ChenDepartment of Pediatrics, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, USA.
Jiebiao WangDepartment of Biostatistics and Health Data Science, University of Pittsburgh, USA.

Funding

Epigenetic Variation and Childhood Asthma in Puerto RicansR01HL117191 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CELEDON, JUAN CARLOS · 2013 to 2020
$5.8M
Statistical methods for population-level cell-type-specific analyses of tissue omics data for Alzheimer's diseaseR01AG080590 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Christopher McKennan, Jiebiao Wang · 2023 to 2026
$1.5M
Integration of GTEx and HuBMAP data to gain population-level cell-type-specific insightsR03OD034501 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JIEBIAO, YAN, QI · 2022 to 2022
$315k
Multi-omics Analysis of Childhood Asthma in HispanicsR21HL150431 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CELEDON, JUAN CARLOS, CHEN, WEI · 2020 to 2021
$235k
NHLBI NIH HHS R01 HL117191NHLBI NIH HHS R21 HL150431NIA NIH HHS R01 AG080590NIH HHS R03 OD034501
6 · The paper itself

Abstract

Cellular deconvolution is a key approach to deciphering the complex cellular makeup of tissues by inferring the composition of cell types from bulk data. Traditionally, deconvolution methods have focused on a single molecular modality, relying either on RNA sequencing (RNA-seq) to capture gene expression or on DNA methylation (DNAm) to reveal epigenetic profiles. While these single-modality approaches have provided important insights, they often lack the depth needed to fully understand the intricacies of cellular compositions, especially in complex tissues. To address these limitations, we introduce EMixed, a versatile framework designed for both single-modality and multi-omics cellular deconvolution. EMixed models raw RNA counts and DNAm counts or frequencies via allocation models that assign RNA transcripts and DNAm reads to cell types, and uses an expectation-maximization (EM) algorithm to estimate parameters. Benchmarking results demonstrate that EMixed significantly outperforms existing methods across both single-modality and multi-modality applications, underscoring the broad utility of this approach in enhancing our understanding of cellular heterogeneity.

Indexed as

cellular deconvolutionDNA methylationEM algorithmgene expressionlatent Dirichlet allocationmulti-omics

Identifiers

PMID41112940
PMCPMC12530062

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.