Name
Title | ||
|---|---|---|
Identification of drug-target interactions via multiple kernel-based triple collaborative matrix factorization |
Abstract | ||
|---|---|---|
Targeted drugs have been applied to the treatment of cancer on a large scale, and some patients have certain therapeutic effects. It is a time-consuming task to detect drug-target interactions (DTIs) through biochemical experiments. At present, machine learning (ML) has been widely applied in large-scale drug screening. However, there are few methods for multiple information fusion. We propose a multiple kernel-based triple collaborative matrix factorization (MK-TCMF) method to predict DTIs. The multiple kernel matrices (contain chemical, biological and clinical information) are integrated via multi-kernel learning (MKL) algorithm. And the original adjacency matrix of DTIs could be decomposed into three matrices, including the latent feature matrix of the drug space, latent feature matrix of the target space and the bi-projection matrix (used to join the two feature spaces). To obtain better prediction performance, MKL algorithm can regulate the weight of each kernel matrix according to the prediction error. The weights of drug side-effects and target sequence are the highest. Compared with other computational methods, our model has better performance on four test data sets. |
Year | DOI | Venue |
|---|---|---|
2022 | 10.1093/bib/bbab582 | BRIEFINGS IN BIOINFORMATICS |
Keywords | DocType | Volume |
bipartite network, drug-target interactions network, multiple kernel learning, matrix factorization, multi-information fusion | Journal | 23 |
Issue | ISSN | Citations |
2 | 1467-5463 | 0 |
PageRank | References | Authors |
0.34 | 0 | 4 |
Name | Order | Citations | PageRank |
|---|---|---|---|
| Yijie Ding | 1 | 0 | 0.34 |
| Jijun Tang | 2 | 370 | 48.23 |
| Fei Guo | 3 | 0 | 0.34 |
| quan zou | 4 | 558 | 67.61 |