Missing-Modality-Aware Graph Neural Network for Cancer Classification
Pith reviewed 2026-05-21 23:41 UTC · model grok-4.3
The pith
A graph neural network connecting patients by shared missing-modality patterns improves cancer classification from incomplete multiomics data.
A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.
Core claim
MAGNET fuses lower-dimensional modality embeddings with a dynamic patient-modality multi-head attention mechanism whose complexity grows linearly with the number of modalities while adapting to each patient's missing-pattern variability. It then constructs a patient graph whose nodes carry these fused embeddings and whose connectivity is set by modality missingness, after which a graph neural network generates the predictions. On three public multiomics datasets containing real-world missingness, this approach outperforms state-of-the-art fusion methods for cancer classification.
What carries the argument
The patient graph whose edges are determined by modality missingness patterns, allowing the subsequent graph neural network to propagate information among patients who share similar data-availability profiles.
If this is right
- All patients with partial modalities can be retained rather than excluded or imputed.
- Fusion cost remains linear rather than combinatorial as the number of modalities grows.
- The model adapts automatically to different missing-pattern distributions without retraining for each pattern.
- Predictions improve by exploiting shared missingness as an additional source of structure in the data.
Where Pith is reading between the lines
- The same graph-construction idea could be applied to other clinical tasks such as survival prediction where missingness may also correlate with outcomes.
- Missingness patterns themselves may serve as a weak but useful proxy for unmeasured patient factors such as disease severity or care access.
- Future experiments could replace the missingness-based edges with edges derived from additional metadata to test whether the current signal is the strongest available.
- The linear scaling property suggests the method remains practical when new modalities are added to existing multiomics collections.
Load-bearing premise
The assumption that connectivity in the patient graph determined by modality missingness patterns provides meaningful signal for the GNN to improve predictions beyond what the fused embeddings alone achieve.
What would settle it
An ablation that removes the graph neural network step and classifies directly from the fused embeddings, then measures whether accuracy drops on the same three datasets, would test whether the missingness-based graph structure adds predictive value.
Figures
read the original abstract
A key challenge in learning from multimodal biological data is missing modalities, where data from one or more modalities are absent for some patients. Existing approaches either exclude patients with missing modalities, impute missing modalities, or make predictions directly with partial modalities. However, most of these methods rely on inflexible, patient-agnostic fusion strategies and do not scale computationally to the combinatorial growth of missing-modality patterns as the number of modalities increases. To address these limitations, we propose MAGNET (Missing-modality-Aware Graph neural NETwork) to enhance multimodal prediction with partial modalities, featuring a dynamic patient-modality multi-head attention mechanism to fuse lower-dimensional modality embeddings based on their contribution and missingness. MAGNET fusion's complexity increases linearly with the number of modalities while adapting to missing-pattern variability. To generate predictions, MAGNET further constructs a patient graph with fused multimodal embeddings as node features and connectivity determined by the modality missingness, followed by a graph neural network. Experiments on three public multiomics datasets for cancer classification, with real-world missingness, show that MAGNET outperforms state-of-the-art fusion methods. The data and code are available at https://github.com/SinaTabakhi/MAGNET.
Editorial analysis
A structured set of objections, weighed in public.
Referee Report
Summary. The manuscript proposes MAGNET, a graph neural network for multimodal cancer classification from multiomics data with missing modalities. It uses a dynamic patient-modality multi-head attention mechanism to fuse lower-dimensional embeddings in a manner whose complexity scales linearly with the number of modalities while conditioning on missingness patterns. A patient graph is constructed with the fused embeddings as node features and edges determined by modality missingness patterns; a GNN is then applied to produce predictions. Experiments on three public multiomics datasets exhibiting real-world missingness report that MAGNET outperforms existing state-of-the-art fusion methods, with code released.
Significance. If the reported gains are shown to arise from the missingness-derived graph rather than the fusion module alone, the work would offer a scalable alternative to imputation or patient exclusion in incomplete multimodal settings. The linear-complexity attention and explicit use of missingness for graph construction are ideas that could transfer to other clinical prediction tasks. Code release supports reproducibility.
major comments (3)
- [Experiments] Experiments section: No ablation isolates the contribution of the patient graph whose connectivity is set by modality missingness patterns. The paper does not compare the full MAGNET model against the same dynamic attention fusion module followed by a non-graph classifier (e.g., MLP or linear layer) on the fused embeddings. Without this control, it remains possible that the headline outperformance is attributable only to the fusion step rather than the GNN operating on missingness-based edges.
- [Experimental Setup] Experimental setup and results: The manuscript provides insufficient detail on baseline re-implementations, hyperparameter tuning protocols, number of independent runs or random seeds, and statistical significance testing (e.g., paired t-tests or confidence intervals). These omissions prevent full verification of the claimed superiority on the three datasets.
- [Method] Method section on patient-graph construction: The assumption that edges defined by shared missingness patterns supply label-relevant structure is not supported by any diagnostic analysis (e.g., comparison of graph properties against random or feature-similarity graphs, or edge-weight correlation with labels). This component is load-bearing for the central claim yet lacks direct evidence.
minor comments (2)
- [Abstract] The abstract states that experiments use 'real-world missingness' but does not quantify the per-modality missing rates or list the exact modalities present in each of the three datasets.
- [Figures] Figure captions and axis labels in the experimental results could be expanded to include the precise missingness percentages and the number of modalities for each dataset.
Simulated Author's Rebuttal
We thank the referee for the constructive and detailed comments. We address each major point below and will revise the manuscript accordingly to strengthen the presentation and evidence.
read point-by-point responses
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Referee: [Experiments] Experiments section: No ablation isolates the contribution of the patient graph whose connectivity is set by modality missingness patterns. The paper does not compare the full MAGNET model against the same dynamic attention fusion module followed by a non-graph classifier (e.g., MLP or linear layer) on the fused embeddings. Without this control, it remains possible that the headline outperformance is attributable only to the fusion step rather than the GNN operating on missingness-based edges.
Authors: We agree that an ablation isolating the graph component is important for validating the central claim. In the revised manuscript we will add a direct comparison of the full MAGNET model against a variant that applies the identical dynamic patient-modality multi-head attention fusion module followed by an MLP (or linear) classifier on the fused embeddings, omitting the GNN and missingness-based edges. This control will clarify the incremental contribution of the patient graph. revision: yes
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Referee: [Experimental Setup] Experimental setup and results: The manuscript provides insufficient detail on baseline re-implementations, hyperparameter tuning protocols, number of independent runs or random seeds, and statistical significance testing (e.g., paired t-tests or confidence intervals). These omissions prevent full verification of the claimed superiority on the three datasets.
Authors: We will expand the experimental setup and results sections (and add an appendix if needed) to provide the requested details: descriptions of baseline re-implementations and any missing-modality adaptations; the hyperparameter search protocol and ranges; the number of independent runs (five runs with distinct random seeds); and statistical significance testing including paired t-tests, p-values, and 95% confidence intervals for all reported metrics. revision: yes
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Referee: [Method] Method section on patient-graph construction: The assumption that edges defined by shared missingness patterns supply label-relevant structure is not supported by any diagnostic analysis (e.g., comparison of graph properties against random or feature-similarity graphs, or edge-weight correlation with labels). This component is load-bearing for the central claim yet lacks direct evidence.
Authors: We accept that direct diagnostic evidence would strengthen the justification for the missingness-based graph. In the revision we will add an analysis that (i) compares structural properties (clustering coefficient, modularity, average degree) of the missingness-derived graph against random graphs and feature-similarity graphs, and (ii) reports the correlation between edge weights (derived from shared missingness) and label agreement across patient pairs. These diagnostics will be presented in a new subsection or appendix. revision: yes
Circularity Check
No circularity: empirical architecture evaluated on external benchmarks
full rationale
The paper presents MAGNET as a new architecture combining dynamic multi-head attention fusion (linear in modalities) with a patient graph whose edges are set by missingness patterns and then processed by a GNN. All performance claims rest on experiments against external baselines on three public multiomics datasets with real missingness. No equations, fitted parameters, or self-citations are shown to reduce the reported gains or the graph-construction step to quantities defined inside the paper itself. The derivation is therefore self-contained and externally falsifiable.
Axiom & Free-Parameter Ledger
axioms (2)
- domain assumption Standard assumptions of supervised classification on tabular multiomics features hold for the cancer datasets used.
- ad hoc to paper The attention mechanism can meaningfully weigh modality contributions conditional on missingness.
Reference graph
Works this paper leans on
-
[1]
Embracing cancer complexity: hallmarks of systemic disease,
C. Swanton, E. Bernard, C. Abbosh, F. Andr ´e, J. Auwerx, A. Balmain, D. Bar-Sagi, R. Bernards, S. Bullman, J. DeGregori et al., “Embracing cancer complexity: hallmarks of systemic disease,” Cell, vol. 187, no. 7, pp. 1589–1616, 2024
work page 2024
-
[2]
C.-H. Yang, S.-H. Moi, L.-Y . Chuang, and Y .-D. Lin, “An information fusion system-driven deep neural networks with application to cancer mortality risk estimate,” IEEE Transactions on Neural Networks and Learning Systems, vol. 36, no. 2, pp. 2905–2916, 2025
work page 2025
-
[3]
X. Su, P. Hu, D. Li, B. Zhao, Z. Niu, T. Herget, P. S. Yu, and L. Hu, “In- terpretable identification of cancer genes across biological networks via transformer-powered graph representation learning,” Nature Biomedical Engineering, pp. 1–19, 2025
work page 2025
-
[4]
Integrative omics for health and disease,
K. J. Karczewski and M. P. Snyder, “Integrative omics for health and disease,” Nature Reviews Genetics , vol. 19, no. 5, pp. 299–310, 2018
work page 2018
-
[5]
J. N. Acosta, G. J. Falcone, P. Rajpurkar, and E. J. Topol, “Multimodal biomedical AI,” Nature Medicine, vol. 28, no. 9, pp. 1773–1784, 2022
work page 2022
-
[6]
M. Zitnik, F. Nguyen, B. Wang, J. Leskovec, A. Goldenberg, and M. M. Hoffman, “Machine learning for integrating data in biology and medicine: principles, practice, and opportunities,” Information Fusion , vol. 50, pp. 71–91, 2019
work page 2019
-
[7]
X.-A. Bi, W. Shen, Y . Shan, D. Chen, L. Xu, K. Chen, and Z. Liu, “MSAFF: multi-way soft attention fusion framework with the large foundation models for the diagnosis of Alzheimer’s disease,” IEEE Transactions on Neural Networks and Learning Systems, pp. 1–15, 2025
work page 2025
-
[8]
Benchmarking joint multi-omics dimensionality reduction approaches for the study of cancer,
L. Cantini, P. Zakeri, C. Hernandez, A. Naldi, D. Thieffry, E. Remy, and A. Baudot, “Benchmarking joint multi-omics dimensionality reduction approaches for the study of cancer,” Nature Communications, vol. 12, no. 1, p. 124, 2021
work page 2021
-
[9]
Similarity network fusion for aggregating data types on a genomic scale,
B. Wang, A. M. Mezlini, F. Demir, M. Fiume, Z. Tu, M. Brudno, B. Haibe-Kains, and A. Goldenberg, “Similarity network fusion for aggregating data types on a genomic scale,” Nature Methods, vol. 11, no. 3, pp. 333–337, 2014
work page 2014
-
[10]
T. Wang, W. Shao, Z. Huang, H. Tang, J. Zhang, Z. Ding, and K. Huang, “MOGONET integrates multi-omics data using graph convolutional networks allowing patient classification and biomarker identification,” Nature Communications, vol. 12, no. 1, p. 3445, 2021
work page 2021
-
[11]
Learning from data with structured missingness,
R. Mitra, S. F. McGough, T. Chakraborti, C. Holmes, R. Copping, N. Hagenbuch, S. Biedermann, J. Noonan, B. Lehmann, A. Shenvi et al., “Learning from data with structured missingness,”Nature Machine Intelligence, vol. 5, no. 1, pp. 13–23, 2023
work page 2023
-
[12]
A review of integrative imputation for multi-omics datasets,
M. Song, J. Greenbaum, J. Luttrell IV , W. Zhou, C. Wu, H. Shen, P. Gong, C. Zhang, and H.-W. Deng, “A review of integrative imputation for multi-omics datasets,” Frontiers in Genetics , vol. 11, p. 570255, 2020
work page 2020
-
[13]
Exploiting interdata relationships in next-generation proteomics analysis,
B. Vitrinel, H. W. Koh, F. M. Kar, S. Maity, J. Rendleman, H. Choi, and C. V ogel, “Exploiting interdata relationships in next-generation proteomics analysis,” Molecular & Cellular Proteomics , vol. 18, no. 8, pp. S5–S14, 2019
work page 2019
-
[14]
Multimodal learning with incomplete modalities by knowledge distillation,
Q. Wang, L. Zhan, P. Thompson, and J. Zhou, “Multimodal learning with incomplete modalities by knowledge distillation,” in Proceedings JOURNAL OF LATEX CLASS FILES, VOL. XX, NO. XX, XXX 2025 11 of the 26th ACM SIGKDD Conference on Knowledge Discovery & Data Mining, 2020, pp. 1828–1838
work page 2025
-
[15]
M3Care: learning with missing modalities in multimodal healthcare data,
C. Zhang, X. Chu, L. Ma, Y . Zhu, Y . Wang, J. Wang, and J. Zhao, “M3Care: learning with missing modalities in multimodal healthcare data,” in Proceedings of the 28th ACM SIGKDD Conference on Knowl- edge Discovery and Data Mining , 2022, pp. 2418–2428
work page 2022
-
[16]
Multimodal patient representation learning with missing modalities and labels,
Z. Wu, A. Dadu, N. Tustison, B. Avants, M. Nalls, J. Sun, and F. Faghri, “Multimodal patient representation learning with missing modalities and labels,” in International Conference on Learning Representations, 2024
work page 2024
-
[17]
V AEs in the presence of missing data,
M. Collier, A. Nazabal, and C. Williams, “V AEs in the presence of missing data,” in ICML Workshop on the Art of Learning with Missing Values (Artemiss), 2020
work page 2020
-
[18]
J. Ngiam, A. Khosla, M. Kim, J. Nam, H. Lee, A. Y . Ng et al. , “Multimodal deep learning.” in Proceedings of the 28th International Conference on Machine Learning , vol. 11, 2011, pp. 689–696
work page 2011
-
[19]
W. Yao, K. Yin, W. K. Cheung, J. Liu, and J. Qin, “DrFuse: learning disentangled representation for clinical multi-modal fusion with missing modality and modal inconsistency,” in Proceedings of the AAAI Confer- ence on Artificial Intelligence , vol. 38, 2024, pp. 16 416–16 424
work page 2024
-
[20]
Handling missing data with graph representation learning,
J. You, X. Ma, Y . Ding, M. J. Kochenderfer, and J. Leskovec, “Handling missing data with graph representation learning,” Advances in Neural Information Processing Systems , vol. 33, pp. 19 075–19 087, 2020
work page 2020
-
[21]
Are multi- modal transformers robust to missing modality?
M. Ma, J. Ren, L. Zhao, D. Testuggine, and X. Peng, “Are multi- modal transformers robust to missing modality?” in Proceedings of the IEEE/CVF Conference on Computer Vision and Pattern Recognition , 2022, pp. 18 177–18 186
work page 2022
-
[22]
MedFuse: multi-modal fusion with clinical time-series data and chest x-ray images,
N. Hayat, K. J. Geras, and F. E. Shamout, “MedFuse: multi-modal fusion with clinical time-series data and chest x-ray images,” in Machine Learning for Healthcare Conference . PMLR, 2022, pp. 479–503
work page 2022
-
[23]
Learning factorized multimodal representations,
Y .-H. H. Tsai, P. P. Liang, A. Zadeh, L.-P. Morency, and R. Salakhutdi- nov, “Learning factorized multimodal representations,” in International Conference on Learning Representations , 2019
work page 2019
-
[24]
SMIL: multimodal learning with severely missing modality,
M. Ma, J. Ren, L. Zhao, S. Tulyakov, C. Wu, and X. Peng, “SMIL: multimodal learning with severely missing modality,” in Proceedings of the AAAI Conference on Artificial Intelligence , vol. 35, 2021, pp. 2302–2310
work page 2021
-
[25]
Robust multimodal learning with missing modalities via parameter-efficient adaptation,
M. K. Reza, A. Prater-Bennette, and M. S. Asif, “Robust multimodal learning with missing modalities via parameter-efficient adaptation,” IEEE Transactions on Pattern Analysis and Machine Intelligence , 2024
work page 2024
-
[26]
K. Lee, S. Lee, S. Hahn, H. Hyun, E. Choi, B. Ahn, and J. Lee, “Learn- ing missing modal electronic health records with unified multi-modal data embedding and modality-aware attention,” in Machine Learning for Healthcare Conference . PMLR, 2023, pp. 423–442
work page 2023
-
[27]
Generating missing values for simulation purposes: a multivariate amputation procedure,
R. M. Schouten, P. Lugtig, and G. Vink, “Generating missing values for simulation purposes: a multivariate amputation procedure,” Journal of Statistical Computation and Simulation , vol. 88, no. 15, pp. 2909–2930, 2018
work page 2018
-
[28]
Y . Zheng, Y . Liu, J. Yang, L. Dong, R. Zhang, S. Tian, Y . Yu, L. Ren, W. Hou, F. Zhu et al. , “Multi-omics data integration using ratio- based quantitative profiling with quartet reference materials,” Nature Biotechnology, vol. 42, no. 7, pp. 1133–1149, 2024
work page 2024
-
[29]
A roadmap for multi-omics data integration using deep learning,
M. Kang, E. Ko, and T. B. Mersha, “A roadmap for multi-omics data integration using deep learning,” Briefings in Bioinformatics , vol. 23, no. 1, p. bbab454, 2022
work page 2022
-
[30]
Multimodal learning for multi-omics: a survey,
S. Tabakhi, M. N. I. Suvon, P. Ahadian, and H. Lu, “Multimodal learning for multi-omics: a survey,” World Scientific Annual Review of Artificial Intelligence, vol. 1, p. 2250004, 2023
work page 2023
-
[31]
Using machine learning approaches for multi-omics data analysis: a review,
P. S. Reel, S. Reel, E. Pearson, E. Trucco, and E. Jefferson, “Using machine learning approaches for multi-omics data analysis: a review,” Biotechnology Advances, vol. 49, p. 107739, 2021
work page 2021
-
[32]
Integrative network fusion: a multi-omics approach in molecular profiling,
M. Chierici, N. Bussola, A. Marcolini, M. Francescatto, A. Zandon `a, L. Trastulla, C. Agostinelli, G. Jurman, and C. Furlanello, “Integrative network fusion: a multi-omics approach in molecular profiling,” Fron- tiers in Oncology , vol. 10, p. 1065, 2020
work page 2020
-
[33]
R. Schulte-Sasse, S. Budach, D. Hnisz, and A. Marsico, “Integration of multiomics data with graph convolutional networks to identify new can- cer genes and their associated molecular mechanisms,” Nature Machine Intelligence, vol. 3, no. 6, pp. 513–526, 2021
work page 2021
-
[34]
Missing data in multi-omics in- tegration: recent advances through artificial intelligence,
J. E. Flores, D. M. Claborne, Z. D. Weller, B.-J. M. Webb-Robertson, K. M. Waters, and L. M. Bramer, “Missing data in multi-omics in- tegration: recent advances through artificial intelligence,” Frontiers in Artificial Intelligence, vol. 6, p. 1098308, 2023
work page 2023
-
[35]
Deep structure integrative representation of multi-omics data for cancer subtyping,
B. Yang, Y . Yang, and X. Su, “Deep structure integrative representation of multi-omics data for cancer subtyping,” Bioinformatics, vol. 38, no. 13, pp. 3337–3342, 2022
work page 2022
-
[36]
Y . Pan, M. Liu, Y . Xia, and D. Shen, “Disease-image-specific learning for diagnosis-oriented neuroimage synthesis with incomplete multi- modality data,” IEEE Transactions on Pattern Analysis and Machine Intelligence, vol. 44, no. 10, pp. 6839–6853, 2021
work page 2021
-
[37]
Multiple imputation after 18+ years,
D. B. Rubin, “Multiple imputation after 18+ years,” Journal of the American Statistical Association , vol. 91, no. 434, pp. 473–489, 1996
work page 1996
-
[38]
Multiple imputation: a primer,
J. L. Schafer, “Multiple imputation: a primer,” Statistical Methods in Medical Research, vol. 8, no. 1, pp. 3–15, 1999
work page 1999
-
[39]
Missing data in clinical research: a tutorial on multiple imputation,
P. C. Austin, I. R. White, D. S. Lee, and S. van Buuren, “Missing data in clinical research: a tutorial on multiple imputation,” Canadian Journal of Cardiology, vol. 37, no. 9, pp. 1322–1331, 2021
work page 2021
-
[40]
TOBMI: trans-omics block missing data imputation using a k-nearest neighbor weighted approach,
X. Dong, L. Lin, R. Zhang, Y . Zhao, D. C. Christiani, Y . Wei, and F. Chen, “TOBMI: trans-omics block missing data imputation using a k-nearest neighbor weighted approach,” Bioinformatics, vol. 35, no. 8, pp. 1278–1283, 2019
work page 2019
-
[41]
Cobolt: integrative analysis of multimodal single-cell sequencing data,
B. Gong, Y . Zhou, and E. Purdom, “Cobolt: integrative analysis of multimodal single-cell sequencing data,” Genome Biology, vol. 22, pp. 1–21, 2021
work page 2021
-
[42]
MultiVI: deep generative model for the integration of multimodal data,
T. Ashuach, M. I. Gabitto, R. V . Koodli, G.-A. Saldi, M. I. Jordan, and N. Yosef, “MultiVI: deep generative model for the integration of multimodal data,” Nature Methods, vol. 20, no. 8, pp. 1222–1231, 2023
work page 2023
-
[43]
Deep adversarial learning for multi-modality missing data completion,
L. Cai, Z. Wang, H. Gao, D. Shen, and S. Ji, “Deep adversarial learning for multi-modality missing data completion,” in Proceedings of the 24th ACM SIGKDD Conference on Knowledge Discovery & Data Mining , 2018, pp. 1158–1166
work page 2018
-
[44]
VIGAN: missing view imputation with generative adversarial networks,
C. Shang, A. Palmer, J. Sun, K.-S. Chen, J. Lu, and J. Bi, “VIGAN: missing view imputation with generative adversarial networks,” in IEEE International Conference on Big Data . IEEE, 2017, pp. 766–775
work page 2017
-
[45]
A flexible generative model for heterogeneous tabular EHR with missing modality,
H. He, W. hao, Y . Xi, Y . Chen, B. Malin, and J. Ho, “A flexible generative model for heterogeneous tabular EHR with missing modality,” in International Conference on Learning Representations , 2024
work page 2024
-
[46]
NEMO: cancer subtyping by integration of partial multi-omic data,
N. Rappoport and R. Shamir, “NEMO: cancer subtyping by integration of partial multi-omic data,” Bioinformatics, vol. 35, no. 18, pp. 3348– 3356, 2019
work page 2019
-
[47]
B. Yang, Y . Yang, M. Wang, and X. Su, “MRGCN: cancer subtyping with multi-reconstruction graph convolutional network using full and partial multi-omics dataset,” Bioinformatics, vol. 39, no. 6, p. btad353, 2023
work page 2023
-
[48]
Augmented sparse representation for incomplete multiview clustering,
J. Chen, S. Yang, X. Peng, D. Peng, and Z. Wang, “Augmented sparse representation for incomplete multiview clustering,” IEEE Transactions on Neural Networks and Learning Systems , vol. 35, no. 3, pp. 4058– 4071, 2022
work page 2022
-
[49]
Inductive representation learning on large graphs,
W. Hamilton, Z. Ying, and J. Leskovec, “Inductive representation learning on large graphs,” Advances in Neural Information Processing Systems, vol. 30, 2017
work page 2017
-
[50]
Graph representation learning,
W. L. Hamilton, “Graph representation learning,” Synthesis Lectures on Artificial Intelligence and Machine Learning , vol. 14, no. 3, pp. 1–159, 2020
work page 2020
-
[51]
L. Van der Maaten and G. Hinton, “Visualizing data using t-SNE,” Journal of Machine Learning Research , vol. 9, no. 11, 2008
work page 2008
-
[52]
The Cancer Genome Atlas Pan-Cancer analysis project,
J. N. Weinstein, E. A. Collisson, G. B. Mills, K. R. Shaw, B. A. Ozenberger, K. Ellrott, I. Shmulevich, C. Sander, and J. M. Stuart, “The Cancer Genome Atlas Pan-Cancer analysis project,” Nature Genetics , vol. 45, no. 10, pp. 1113–1120, 2013
work page 2013
-
[53]
P.-K. Raj-Kumar, J. Liu, J. A. Hooke, A. J. Kovatich, L. Kvecher, C. D. Shriver, and H. Hu, “PCA-PAM50 improves consistency between breast cancer intrinsic and clinical subtyping reclassifying a subset of luminal A tumors as luminal B,” Scientific Reports, vol. 9, no. 1, p. 7956, 2019
work page 2019
-
[54]
Comprehensive molec- ular characterization of urothelial bladder carcinoma,
The Cancer Genome Atlas Research Network, “Comprehensive molec- ular characterization of urothelial bladder carcinoma,” Nature, vol. 507, no. 7492, p. 315, 2014
work page 2014
-
[55]
Y . El-Manzalawy, T.-Y . Hsieh, M. Shivakumar, D. Kim, and V . Honavar, “Min-redundancy and max-relevance multi-view feature selection for predicting ovarian cancer survival using multi-omics data,” BMC Med- ical Genomics, vol. 11, no. 3, pp. 19–31, 2018
work page 2018
-
[56]
Visualizing and interpreting cancer genomics data via the Xena platform,
M. J. Goldman, B. Craft, M. Hastie, K. Repe ˇcka, F. McDade, A. Kamath, A. Banerjee, Y . Luo, D. Rogers, A. N. Brooks et al. , “Visualizing and interpreting cancer genomics data via the Xena platform,” Nature Biotechnology, vol. 38, no. 6, pp. 675–678, 2020
work page 2020
-
[57]
E. R. Girden, ANOVA: repeated measures. Sage, 1992, no. 84
work page 1992
-
[58]
Adam: a method for stochastic optimization,
D. P. Kingma and J. Ba, “Adam: a method for stochastic optimization,” in International Conference on Learning Representations , 2015
work page 2015
-
[59]
Silhouettes: a graphical aid to the interpretation and validation of cluster analysis,
P. J. Rousseeuw, “Silhouettes: a graphical aid to the interpretation and validation of cluster analysis,” Journal of Computational and Applied Mathematics, vol. 20, pp. 53–65, 1987. JOURNAL OF LATEX CLASS FILES, VOL. XX, NO. XX, XXX 2025 12
work page 1987
-
[60]
D. L. Davies and D. W. Bouldin, “A cluster separation measure,” IEEE Transactions on Pattern Analysis and Machine Intelligence , vol. PAMI- 1, no. 2, pp. 224–227, 1979
work page 1979
-
[61]
S. Ma, “Dataset for ”moving towards genome-wide data integration for patient stratification with integrate any omics”,” Oct. 2024, Zenodo. [Online]. Available: https://doi.org/10.5281/zenodo.13989262
-
[62]
Moving towards genome-wide data integration for patient stratification with integrate any omics,
S. Ma, A. G. Zeng, B. Haibe-Kains, A. Goldenberg, J. E. Dick, and B. Wang, “Moving towards genome-wide data integration for patient stratification with integrate any omics,” Nature Machine Intelligence , vol. 7, no. 1, pp. 29–42, 2025
work page 2025
-
[63]
P. Veli ˇckovi´c, G. Cucurull, A. Casanova, A. Romero, P. Li `o, and Y . Bengio, “Graph attention networks,” in International Conference on Learning Representations, 2018
work page 2018
-
[64]
Semi-supervised classification with graph convolutional networks,
T. N. Kipf and M. Welling, “Semi-supervised classification with graph convolutional networks,” in International Conference on Learning Rep- resentations, 2017
work page 2017
-
[65]
How powerful are graph neural networks?
K. Xu, W. Hu, J. Leskovec, and S. Jegelka, “How powerful are graph neural networks?” in International Conference on Learning Represen- tations, 2019
work page 2019
-
[66]
Tune: A Research Platform for Distributed Model Selection and Training
R. Liaw, E. Liang, R. Nishihara, P. Moritz, J. E. Gonzalez, and I. Stoica, “Tune: a research platform for distributed model selection and training,” arXiv preprint arXiv:1807.05118 , 2018
work page internal anchor Pith review Pith/arXiv arXiv 2018
-
[67]
A system for massively parallel hyperpa- rameter tuning,
L. Li, K. Jamieson, A. Rostamizadeh, E. Gonina, J. Ben-Tzur, M. Hardt, B. Recht, and A. Talwalkar, “A system for massively parallel hyperpa- rameter tuning,” Proceedings of Machine Learning and Systems , vol. 2, pp. 230–246, 2020. JOURNAL OF LATEX CLASS FILES, VOL. XX, NO. XX, XXX 2025 13 Supplementary Material APPENDIX A. Hyperparameter Tuning To ensure ...
work page 2020
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