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doi: 10.1038/s41540-019-0086-3 , 10.3929/ethz-b-000331766 , 10.5281/zenodo.3374413 , 10.5281/zenodo.3374412 , 10.48550/arxiv.1803.11274
pmid: 30854223
pmc: PMC6401099
arXiv: 1803.11274
handle: 20.500.11850/331766
doi: 10.1038/s41540-019-0086-3 , 10.3929/ethz-b-000331766 , 10.5281/zenodo.3374413 , 10.5281/zenodo.3374412 , 10.48550/arxiv.1803.11274
pmid: 30854223
pmc: PMC6401099
arXiv: 1803.11274
handle: 20.500.11850/331766
AbstractReliable identification of molecular biomarkers is essential for accurate patient stratification. While state-of-the-art machine learning approaches for sample classification continue to push boundaries in terms of performance, most of these methods are not able to integrate different data types and lack generalization power, limiting their application in a clinical setting. Furthermore, many methods behave as black boxes, and we have very little understanding about the mechanisms that lead to the prediction. While opaqueness concerning machine behavior might not be a problem in deterministic domains, in health care, providing explanations about the molecular factors and phenotypes that are driving the classification is crucial to build trust in the performance of the predictive system. We propose Pathway-Induced Multiple Kernel Learning (PIMKL), a methodology to reliably classify samples that can also help gain insights into the molecular mechanisms that underlie the classification. PIMKL exploits prior knowledge in the form of a molecular interaction network and annotated gene sets, by optimizing a mixture of pathway-induced kernels using a Multiple Kernel Learning (MKL) algorithm, an approach that has demonstrated excellent performance in different machine learning applications. After optimizing the combination of kernels to predict a specific phenotype, the model provides a stable molecular signature that can be interpreted in the light of the ingested prior knowledge and that can be used in transfer learning tasks.
FOS: Computer and information sciences, Molecular Networks (q-bio.MN), Computational Biology, Machine Learning (stat.ML), Article, Pattern Recognition, Automated, Machine Learning, Statistics - Machine Learning, FOS: Biological sciences, Biomarkers, Tumor, Humans, Quantitative Biology - Molecular Networks, multiple kernel learning, Algorithms, Software
FOS: Computer and information sciences, Molecular Networks (q-bio.MN), Computational Biology, Machine Learning (stat.ML), Article, Pattern Recognition, Automated, Machine Learning, Statistics - Machine Learning, FOS: Biological sciences, Biomarkers, Tumor, Humans, Quantitative Biology - Molecular Networks, multiple kernel learning, Algorithms, Software
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
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