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Zhenglong Cheng

dblp:426/1941 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2025
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis › cell clustering
cell type clustering
0.912025
scMGCL: accurate and efficient integration representation of single-cell multi-omics data · Bioinform. 2025
Bioinformatics and computational biology › single-cell analysis › cell clustering
single-cell clustering
0.912025
scMGCL: accurate and efficient integration representation of single-cell multi-omics data · Bioinform. 2025
Bioinformatics and computational biology › single-cell analysis › single-cell data integration
single-cell multi-omics integration
0.912025
scMGCL: accurate and efficient integration representation of single-cell multi-omics data · Bioinform. 2025

Methods — techniques the papers use, named apart from their topics

self-supervised learning · 0.9graph contrastive learning · 0.9
YearPublicationVenuePosition
2025 scMGCL: accurate and efficient integration representation of single-cell multi-omics data
abstract
MOTIVATION: Single-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. RESULTS: Benchmarking 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.
Zhenglong Cheng, Risheng Lu, Shixiong Zhang 0002
Bioinform.1