Demo Data from EDBT 2026 / reviewers in the wild / expert
Lingyi Hu
dblp:425/2999
· DBLP profile ↗
1ranked-venue papers
0as 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 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 · 67% Computational science and engineering · 33% |
Topics — the 3 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › network bioinformatics › biological network analysis › biological network inference
gene network inference |
0.9 | 1 | 2025 | AJGM: joint learning of heterogeneous gene networks with adaptive graphical model · Bioinform. 2025 |
Computational science and engineering
graphical models |
0.9 | 1 | 2025 | AJGM: joint learning of heterogeneous gene networks with adaptive graphical model · Bioinform. 2025 |
Bioinformatics and computational biology › single-cell analysis › single-cell RNA sequencing
single-cell RNA-seq analysis |
0.9 | 1 | 2025 | AJGM: joint learning of heterogeneous gene networks with adaptive graphical model · Bioinform. 2025 |
Methods — techniques the papers use, named apart from their topics
gaussian graphical model · 0.9adaptive weighting · 0.9
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | AJGM: joint learning of heterogeneous gene networks with adaptive graphical modelabstractMOTIVATION: Inferring gene networks provides insights into biological pathways and functional relationships among genes. When gene expression samples exhibit heterogeneity, they may originate from unknown subtypes, prompting the utilization of mixture Gaussian graphical model (GGM) for simultaneous subclassification and gene network inference. However, this method overlooks the heterogeneity of network relationships across subtypes and does not sufficiently emphasize shared relationships. Additionally, GGM assumes data follows a multivariate Gaussian distribution, which is often not the case with zero-inflated scRNA-seq data. RESULTS: We propose an Adaptive Joint Graphical Model (AJGM) for estimating multiple gene networks from single-cell or bulk data with unknown heterogeneity. In AJGM, an overall network is introduced to capture relationships shared by all samples. The model establishes connections between the subtype networks and the overall network through adaptive weights, enabling it to focus more effectively on gene relationships shared across all networks, thereby enhancing the accuracy of network estimation. On synthetic data, the proposed approach outperforms existing methods in terms of sample classification and network inference, particularly excelling in the identification of shared relationships. Applying this method to gene expression data from triple-negative breast cancer confirms known gene pathways and hub genes, while also revealing novel biological insights. AVAILABILITY AND IMPLEMENTATION: The Python code and demonstrations of the proposed approaches are available at https://github.com/yyytim/AJGM, and the software is archived in Zenodo with DOI: 10.5281/zenodo.14740972. Shunqi Yang, Lingyi Hu, Pengzhou Chen, Xiangxiang Zeng, Shanjun Mao |
Bioinform. | 2 |