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Qinggang Niu

dblp:430/7441 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2026
—ORCID · none

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

Artificial intelligence and machine learning · 1 · 1 since 2021Graphics, computer vision, multimedia, augmented reality and games · 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
Medical and health informatics · 77% Bioinformatics and computational biology · 23%

Topics — the 4 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Medical and health informatics › clinical prediction
cancer survival analysis
1.012026
Cancer Survival Prediction by Cyclic Generation and Multi-grained Alignment · AAAI 2026
Medical and health informatics › clinical prediction
multimodal survival prediction
1.012026
Cancer Survival Prediction by Cyclic Generation and Multi-grained Alignment · AAAI 2026
Bioinformatics and computational biology
genomics
0.312026
Cancer Survival Prediction by Cyclic Generation and Multi-grained Alignment · AAAI 2026
Bioinformatics and computational biology › systems bioinformatics
pathway analysis
0.312026
Cancer Survival Prediction by Cyclic Generation and Multi-grained Alignment · AAAI 2026

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

multi-grained multimodal alignment · 1.0cyclic modality generation · 1.0adaptive fusion · 1.0
YearPublicationVenuePosition
2026 Cancer Survival Prediction by Cyclic Generation and Multi-grained Alignment
abstract
Cancer survival analysis with multimodal data is crucial for precise treatments and patient benefits. However, the following challenges prohibit integrating histopathology and genomics: (i) multimodal data is not always complete, especially for the more costly genomics data; (ii) intricate interactions between different modalities are difficult to capture and understand. To response, we propose an end-to-end framework (CIMA) that coordinates Cyclic modality generation and Multi-grained multimodal Alignment. Specifically, CIMA designs a cyclic modality reconstruction module to reciprocally impute missing modalities and infer the interactions between them. Next, it introduces the multi-grained alignment module over the imputed data and interactions to mine fine-grained alignments between histopathology (slide patches) and genomics (biological pathways). CIMA then constructs the adaptive fusion module to leverage multimodal data and alignments for survival prediction. Extensive experiments on cancer benchmark datasets demonstrate that CIMA outperforms existing methods and exhibits good interpretability, providing valuable insights into intricate relationships between pathological phenotypes and biological pathways.Our code is released in the supplementary materials.
Yongqi Bu, Qinggang Niu, Jun Wang 0035, Guoxian Yu
AAAI2