Evidence map›Paper›PMID 39252099›Full record

ArticleGenome biology2024

Dimension reduction, cell clustering, and cell-cell communication inference for single-cell transcriptomics with DcjComm.

Qian Ding, Wenyi Yang, Guangfu Xue, Hongxin Liu, Yideng Cai, Jinhao Que, Xiyun Jin, Meng Luo, Fenglan Pang, Yuexin Yang and 7 more

Abstract read
In one paragraph

Article in Genome biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

17 authors.

Qian Ding *Center for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Wenyi Yang *Center for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Guangfu Xue *Center for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Hongxin LiuCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Yideng CaiCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Jinhao QueCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Xiyun JinSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China.
Meng LuoCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Fenglan PangCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Yuexin YangCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China.
Yi LinSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China.
Yusong LiuSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China.
Haoxiu SunSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China.
Renjie TanSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China.
Pingping WangSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China. wangpingping@hrbmu.edu.cn.
Zhaochun XuSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150076, China. zhaochunxu@hrbmu.edu.cn.
Qinghua JiangCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150000, China. qhjiang@hit.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in single-cell transcriptomics provide an unprecedented opportunity to explore complex biological processes. However, computational methods for analyzing single-cell transcriptomics still have room for improvement especially in dimension reduction, cell clustering, and cell-cell communication inference. Herein, we propose a versatile method, named DcjComm, for comprehensive analysis of single-cell transcriptomics. DcjComm detects functional modules to explore expression patterns and performs dimension reduction and clustering to discover cellular identities by the non-negative matrix factorization-based joint learning model. DcjComm then infers cell-cell communication by integrating ligand-receptor pairs, transcription factors, and target genes. DcjComm demonstrates superior performance compared to state-of-the-art methods.

Indexed as

Cell CommunicationSingle-Cell AnalysisTranscriptomeCluster AnalysisComputational BiologyGene Expression ProfilingHumansCell–cell communicationCell clusteringJoint learningNon-negative matrix factorizationSingle-cell

Identifiers

PMID39252099
PMCPMC11382422

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.