ArticleFrontiers in genetics2020
Integrating Somatic Mutations for Breast Cancer Survival Prediction Using Machine Learning Methods.
Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- BRCAGenie: A machine learning-driven 43-gene polygenic risk score model for precision prediction of breast cancer survival.Journal of translational medicine · 2025Article
- Survival prediction and molecular subtyping of squamous cell lung cancer based on network embedding.Scientific reports · 2024Article
- Uncertainty quantification in multi-class image classification using chest X-ray images of COVID-19 and pneumonia.Frontiers in artificial intelligence · 2024Article
- Secure tumor classification by shallow neural network using homomorphic encryption.BMC genomics · 2022Article
- A survey on multi-omics-based cancer diagnosis using machine learning with the potential application in gastrointestinal cancer.Frontiers in medicine · 2022Review
- Integration strategies of multi-omics data for machine learning analysis.Computational and structural biotechnology journal · 2021Review
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Authors and funding
4 authors.
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Abstract
Breast cancer is the most common malignancy in women, and because it has a high mortality rate, it is urgent to develop computational methods to increase the accuracy of breast cancer survival predictive models. Although multi-omics data such as gene expression have been extensively used in recent studies, the accurate prognosis of breast cancer remains a challenge. Somatic mutations are another important and promising data source for studying cancer development, and its effect on the prognosis of breast cancer remains to be further explored. Meanwhile, these omics datasets are high-dimensional and redundant. Therefore, we adopted multiple kernel learning (MKL) to efficiently integrate somatic mutation to currently molecular data including gene expression, copy number variation (CNV), methylation, and protein expression data for the prediction of breast cancer survival. Before integration, the maximum relevance minimum redundancy (mRMR) feature selection method was utilized to select features that present high relevance to survival and low redundancy among themselves for each type of data. The experimental results demonstrated that the proposed method achieved the most optimal performance and there was a remarkable improvement in the prediction performance when somatic mutations were included, indicating that somatic mutations are critical for improving breast cancer survival predictions. Moreover, mRMR was superior to other feature selection methods used in previous studies. Furthermore, MKL outperformed the other traditional classifiers in multi-omics data integration. Our analysis indicated that through employing promising omics data such as somatic mutations and harnessing the power of proper feature selection methods and effective integration frameworks, the breast cancer survival predictive accuracy can be further increased, thereby providing a more optimal clinical diagnosis and more effective treatment for breast cancer patients.
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