Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Qinghua Ran

dblp:262/6144 · DBLP profile ↗
← Back
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

TopicWeightPapersLastEvidence papers
Machine learning › Trustworthy machine learning › robustness
learning with noisy labels
1.012026
Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series Learning · KDD (1) 2026
Machine learning › Trustworthy machine learning
robustness
1.012026
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
1.012026
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
0.912025
Benchmarking algorithms for spatially variable gene identification in spatial transcriptomics · Bioinform. 2025
Bioinformatics and computational biology › transcriptomics
spatial transcriptomics
0.912025
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
0.312026
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
YearPublicationVenuePosition
2026 Dual Data-centric Separation with Circular Mixup for Noise-resistant Time Series Learning
abstract
Deep 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 Supervision
abstract
This 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
NeurIPS3
2025 Benchmarking algorithms for spatially variable gene identification in spatial transcriptomics
abstract
MOTIVATION: 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