Evidence map›Paper›PMID 40632608›Full record

ArticleBioinformatics (Oxford, England)2025

scMGCL: accurate and efficient integration representation of single-cell multi-omics data.

Zhenglong Cheng, Risheng Lu, Shixiong Zhang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Article
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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

3 authors.

Zhenglong ChengSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.
Risheng LuSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.
Shixiong ZhangSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.ORCID 0000-0002-0314-9199

Funding

National Natural Science Foundation of China 62102294
6 · The paper itself

Abstract

motivationSingle-cell multi-omics data integration is essential for understanding cellular states and disease mechanisms, yet integrating heterogeneous data modalities remains a challenge. We present scMGCL, a graph contrastive learning framework for robust integration of single-cell ATAC-seq and RNA-seq data. Our approach leverages self-supervised learning on cell-cell similarity graphs, in which each modality's graph structure serves as an augmentation for the other. This cross-modality contrastive paradigm enables the learning of biologically meaningful, shared representations while preserving modality-specific features.

resultsBenchmarking against state-of-the-art methods demonstrates that scMGCL outperforms others in cell-type clustering, label transfer accuracy, and preservation of marker-gene correlations. Additionally, scMGCL significantly improves computational efficiency, reducing runtime and memory usage. The method's effectiveness is further validated through extensive analyses of cell-type similarity and functional consistency, providing a powerful tool for multi-omics data exploration. AVAILABILITY AND IMPLEMENTATION: Code and datasets are released at https://github.com/zlCreator/scMGCL.

Indexed as

Computational BiologyGenomicsSingle-Cell AnalysisSoftwareAlgorithmsChromatin Immunoprecipitation SequencingHumansMultiomicsRNA-Seq

Identifiers

PMID40632608
PMCPMC12308176

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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.