Demo Data from EDBT 2026 / reviewers in the wild / expert
Qinghua Ran
dblp:262/6144
· DBLP profile ↗
3ranked-venue papers
0as first author
3since 2021 · last 2026
—ORCID · conflict
Domains — the database's venue-derived domains; a paper can count in several
Artificial intelligence and machine learning · 2 · 2 since 2021Databases, data management, data science and information retrieval · 1 · 1 since 2021Applied, 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.
| Artificial intelligence
1 paper |
Trustworthy machine learning · 61% Representation and self-supervised learning · 30% Time series and sequential data · 9% | |
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 6 heaviest of 8, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Machine learning › Trustworthy machine learning › robustness
learning with noisy labels |
1.0 | 1 | 2026 | Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series Learning · KDD (1) 2026 |
Machine learning › Trustworthy machine learning
robustness |
1.0 | 1 | 2026 | Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series Learning · KDD (1) 2026 |
Machine learning › Representation and self-supervised learning › representation learning › sequence representation learning
time series representation learning |
1.0 | 1 | 2026 | Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series Learning · KDD (1) 2026 |
Bioinformatics and computational biology › transcriptomics › spatial transcriptomics
spatially variable gene detection |
0.9 | 1 | 2025 | Benchmarking algorithms for spatially variable gene identification in spatial transcriptomics · Bioinform. 2025 |
Bioinformatics and computational biology › transcriptomics
spatial transcriptomics |
0.9 | 1 | 2025 | Benchmarking algorithms for spatially variable gene identification in spatial transcriptomics · Bioinform. 2025 |
Machine learning › Time series and sequential data › time series analysis
time series learning |
0.3 | 1 | 2026 | Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series Learning · KDD (1) 2026 |
Methods — techniques the papers use, named apart from their topics
pseudo-labeling · 1.0mixup · 1.0contrastive learning · 1.0
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2026 | Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series LearningabstractDeep neural networks (DNNs) have achieved extensive progress in time series learning. However, they could suffer from performance degradation when it comes to label noise in the real world. Towards this end, this paper studies an underexplored yet realistic problem of noise-resistant time series learning and proposes a novel data-centric approach named Dual Data-centric Separation with Circular Mixup (DREAM) for this problem. The core of our DREAM is to explore and exploit the noisy data from dual data-centric views for reduced overfitting. On the one hand, we assume that samples with similar features share similar labels and infer the pseudo label of each sample using its affinity graph to capture the corresponding pseudo margin. On the other hand, we monitor the optimization status by simulating the mislabeled data to generate flexible criteria for accurate separation of clean and noisy samples. In addition, we leverage circular Mixup to interpolate between clean and noisy samples in the embedding space. These mixed samples are incorporated into a discrepancy-aware consistency learning framework to ensure robust time series representations of all the separated samples. Experimental results on a wide range of publicly accessible datasets reveal the effectiveness of our DREAM. Yuhang Pei 0001, Fanchun Meng, Qinghua Ran, Tao Ren 0002, Yifan Wang 0014, Wei Ju 0001, Zimo Wang, Xian-Sheng Hua 0001, Xiao Luo 0001 |
KDD (1) | 3 |
| 2025 | SEGA: Shaping Semantic Geometry for Robust Hashing under Noisy SupervisionabstractThis paper studies the problem of learning hash codes from noisy supervision, which is a practical yet challenging task. This problem is important in extensive real-world applications such as image retrieval and cross-modal retrieval. However, most of the existing methods focus on label denoising to address this problem, but ignore the geometric structure of the hash space, which is critical for learning stable hash codes. Towards this end, this paper proposes a novel framework named Semantic Geometry Shaping (SEGA) that explicitly refines the semantic geometry of hash space. Specifically, we first learn dynamic class prototypes as semantic anchors and cluster hash embeddings around these prototypes to keep structural stability. We then leverage both the energy of predicted distributions and structure-based divergence to estimate the uncertainty of instances and calibrate the supervision in a soft manner. Moreover, we introduce structure-aware interpolation to improve the class boundaries. To verify the effectiveness of our design, we give the theoretical analysis for the proposed framework. Experiments on a range of widely-used retrieval datasets justify the superiority of our SEGA over extensive strong baselines under noisy supervision. Yiyang Gu, Bohan Wu, Qinghua Ran, Rongcheng Tu, Xiao Luo 0001, Zhiping Xiao 0001, Wei Ju 0001, Dacheng Tao, Ming Zhang 0004 |
NeurIPS | 3 |
| 2025 | Benchmarking algorithms for spatially variable gene identification in spatial transcriptomicsabstractMOTIVATION: The rapid development of spatial transcriptomics has underscored the importance of identifying spatially variable genes. As a fundamental task in spatial transcriptomic data analysis, spatially variable gene identification has been extensively studied. However, the lack of comprehensive benchmark makes it difficult to validate the effectiveness of various algorithms scattered across a large number of studies with real-world datasets. RESULTS: In response, this article proposes a benchmark framework to evaluate algorithms for identifying spatially variable genes through the analysis of 30 synthesized and 74 real-world datasets, aiming to identify the best algorithms and their corresponding application scenarios. This framework can assist medical and life scientists in selecting suitable algorithms for their research, while also aid bioinformatics scientists in developing more powerful and efficient computational methods in spatial transcriptomic research. AVAILABILITY AND IMPLEMENTATION: The source code of this benchmarking framework is available at both Github (https://github.com/XiDsLab/svg-benchmark) and Zenodo (https://doi.org/10.5281/zenodo.15031083). In addition, all real and synthetic datasets considered in this study are also publicly available at Zenodo (https://doi.org/10.5281/zenodo.7227771). Xuanwei Chen, Qinghua Ran, Xingjie Shi, Ruibin Xi |
Bioinform. | 2 |