TY - JOUR
T1 - Graph-based representation for specificity and heterogeneity in biomedical multi-view learning
AU - Feng, Shuang
AU - Wan, Xiaohua
AU - Li, Chang
AU - Liu, Simeng
AU - Liu, Shuxian
AU - Wang, Letian
AU - Zhuang, Xiahai
AU - Zhang, Fa
AU - Hu, Bin
N1 - Publisher Copyright:
© 2026 Elsevier B.V.
PY - 2027/2
Y1 - 2027/2
N2 - Biomedical multi-view learning (BioMVL) has shown promise for disease classification by integrating complementary information across views. However, existing methods often overlook the specificity of each view and the semantic heterogeneity across multi-view data, limiting representation quality and interpretability. To address these problems, this paper presents a novel specificity-heterogeneity BioMVL framework (SH-BioMVL). The framework employs a global-local graph neural network (GLGNN) to disentangle the interactivity and specificity information in multi-view data. Additionally, the LD-based individual genetic graph construction method (LDIG) transforms high-dimensional genetic sequences into biologically informed representations to facilitate heterogeneous fusion. Experimental validation across different cohorts, modalities, and diseases demonstrates that SH-BioMVL achieves state-of-the-art performance and maintains robust generalization in biomedical multi-view disease classification tasks. Analysis of cross-view interactivity and specificity features further confirms the biological validity and reliability. Overall, SH-BioMVL provides an effective framework for addressing specificity and heterogeneity in BioMVL, offering strong support for solving biomedical problems.
AB - Biomedical multi-view learning (BioMVL) has shown promise for disease classification by integrating complementary information across views. However, existing methods often overlook the specificity of each view and the semantic heterogeneity across multi-view data, limiting representation quality and interpretability. To address these problems, this paper presents a novel specificity-heterogeneity BioMVL framework (SH-BioMVL). The framework employs a global-local graph neural network (GLGNN) to disentangle the interactivity and specificity information in multi-view data. Additionally, the LD-based individual genetic graph construction method (LDIG) transforms high-dimensional genetic sequences into biologically informed representations to facilitate heterogeneous fusion. Experimental validation across different cohorts, modalities, and diseases demonstrates that SH-BioMVL achieves state-of-the-art performance and maintains robust generalization in biomedical multi-view disease classification tasks. Analysis of cross-view interactivity and specificity features further confirms the biological validity and reliability. Overall, SH-BioMVL provides an effective framework for addressing specificity and heterogeneity in BioMVL, offering strong support for solving biomedical problems.
KW - Biomedical multi-view learning
KW - Genetic-imaging data fusion
KW - Graph neural network
KW - Specificity and heterogeneity
UR - https://www.scopus.com/pages/publications/105049059396
U2 - 10.1016/j.inffus.2026.104734
DO - 10.1016/j.inffus.2026.104734
M3 - Article
AN - SCOPUS:105049059396
SN - 1566-2535
VL - 138
JO - Information Fusion
JF - Information Fusion
M1 - 104734
ER -