Demo Data from VLDB 2026 / reviewers in the wild / expert
Zhenglong Cheng
dblp:426/1941
· DBLP profile ↗
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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › single-cell analysis › cell clustering
cell type clustering |
0.9 | 1 | 2025 | 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 |
0.9 | 1 | 2025 | 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 |
0.9 | 1 | 2025 | 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
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | scMGCL: accurate and efficient integration representation of single-cell multi-omics dataabstractMOTIVATION: 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 |