Fast Kronecker product kernel methods via generalized vec trick
Not on the map. Why?
Abstract (arXiv)
Kronecker product kernel provides the standard approach in the kernel methods literature for learning from graph data, where edges are labeled and both start and end vertices have their own feature representations. The methods allow generalization to such new edges, whose start and end vertices do not appear in the training data, a setting known as zero-shot or zero-data learning. Such a setting occurs in numerous applications, including drug-target interaction prediction, collaborative filtering and information retrieval. Efficient training algorithms based on the so-called vec trick, that makes use of the special structure of the Kronecker product, are known for the case where the training data is a complete bipartite graph. In this work we generalize these results to non-complete training graphs. This allows us to derive a general framework for training Kronecker product kernel methods, as specific examples we implement Kronecker ridge regression and support vector machine algorithms. Experimental results demonstrate that the proposed approach leads to accurate models, while allowing order of magnitude improvements in training and prediction time.
Key facts. Cited by 3 papers in the map (data through 7 Oct 2026). First posted on arXiv 7 Jan 2016.
Builds on
No reference list yet.
Built on by
Citing papers per year: 2021: 1; 2022: 0; 2023: 0; 2024: 0; 2025: 1; 2026: 1.
3 papers.
- 2021Optimizing Area Under the Curve Measures via Matrix Factorization for Predicting Drug-Target Interaction with Multiple Similaritiescited by 2
- 2025Interaction Concordance Index: Performance Evaluation for Interaction Prediction Methodscited by 1
- 2026Scalable Pairwise Kernel Learning with Stochastic Vec Trickcited by 0
- 2026Scalable Pairwise Kernel Learning with Stochastic Vec Trick15 Jun 2026
- 2025Interaction Concordance Index: Performance Evaluation for Interaction Prediction Methods16 Oct 2025
- 2021Optimizing Area Under the Curve Measures via Matrix Factorization for Predicting Drug-Target Interaction with Multiple Similarities1 May 2021