Evidence map›Paper›PMID 36110899›Full record

ArticleNAR genomics and bioinformatics2022

Celda: a Bayesian model to perform co-clustering of genes into modules and cells into subpopulations using single-cell RNA-seq data.

Zhe Wang, Shiyi Yang, Yusuke Koga, Sean E Corbett, Conor V Shea, W Evan Johnson, Masanao Yajima, Joshua D Campbell

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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  4. MMP8 Promotes NETosis in Gestational Diabetes Mellitus.Antioxidants (Basel, Switzerland) · 2026
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  10. Neonatal liver niches program T cell tolerance.bioRxiv : the preprint server for biology · 2026
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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

8 authors.

Zhe WangBioinformatics Program, Boston University, Boston, MA, USA.ORCID https://orcid.org/0000-0001-7071-3370
Shiyi YangDivision of Computational Biomedicine, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Yusuke KogaBioinformatics Program, Boston University, Boston, MA, USA.
Sean E CorbettBioinformatics Program, Boston University, Boston, MA, USA.
Conor V SheaBioinformatics Program, Boston University, Boston, MA, USA.
W Evan JohnsonBioinformatics Program, Boston University, Boston, MA, USA.
Masanao YajimaDepartment of Mathematics and Statistics, Boston University, Boston, MA, USA.
Joshua D CampbellBioinformatics Program, Boston University, Boston, MA, USA.

Funding

Removing batch effects in high-throughput biomedical studiesR01GM127430 · NIGMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI William Evan Johnson · 2018 to 2026
$2.4M
An interactive analysis toolkit for single cell RNA-seq in cancer researchU01CA220413 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JOHNSON, WILLIAM EVAN · 2017 to 2019
$1.2M
Integrative clustering of cells and samples using multi-modal single-cell dataR01LM013154 · NLM · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CAMPBELL, JOSHUA D, YAJIMA, MASANAO · 2019 to 2021
$1.1M
NCI NIH HHS U01 CA220413NIGMS NIH HHS R01 GM127430NLM NIH HHS R01 LM013154
6 · The paper itself

Abstract

Single-cell RNA-seq (scRNA-seq) has emerged as a powerful technique to quantify gene expression in individual cells and to elucidate the molecular and cellular building blocks of complex tissues. We developed a novel Bayesian hierarchical model called Cellular Latent Dirichlet Allocation (Celda) to perform co-clustering of genes into transcriptional modules and cells into subpopulations. Celda can quantify the probabilistic contribution of each gene to each module, each module to each cell population and each cell population to each sample. In a peripheral blood mononuclear cell dataset, Celda identified a subpopulation of proliferating T cells and a plasma cell which were missed by two other common single-cell workflows. Celda also identified transcriptional modules that could be used to characterize unique and shared biological programs across cell types. Finally, Celda outperformed other approaches for clustering genes into modules on simulated data. Celda presents a novel method for characterizing transcriptional programs and cellular heterogeneity in scRNA-seq data.

Identifiers

PMID36110899
PMCPMC9469931

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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.