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Robust Transfer Learning for High-Dimensional GLM Using γ $$ \gamma $$ -Divergence With Applications to Cancer
Fuzhi Xu1,2, Shuangge Ma3, Qingzhao Zhang2,4
1International Institute of Finance, School of Management, University of Science and Technology of China, Anhui, China.
This study introduces a robust transfer learning method for analyzing complex diseases using high-dimensional genomic data. It effectively handles data outliers and contamination, improving risk assessment and biomarker detection in cancer research.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- High-dimensional profiling data is crucial for complex disease analysis, risk assessment, and biomarker discovery.
- Limited sample sizes in cancer genomics studies necessitate information borrowing from external data sources.
- Existing transfer learning methods lack robustness to outliers and data contamination common in biomedical data.
Purpose of the Study:
- To develop a robust transfer learning approach for high-dimensional genomic data analysis.
- To address the limitations of existing methods regarding data outliers and contamination.
- To improve estimation and prediction accuracy in complex disease studies.
Main Methods:
- Proposed a robust transfer learning method using minimum γ-divergence within a generalized linear model (GLM) framework.
- Incorporated a data-driven source detection scheme to identify informative sources and prevent negative transfer.
- Developed a computationally efficient algorithm based on proximal gradient descent for transfer and debiasing.
Main Results:
- Established theoretical guarantees including consistency and high-dimensional estimation error bounds.
- Demonstrated superior and competitive performance in selection, prediction, and classification via simulations.
- Validated practical utility on real-world breast cancer and glioblastoma genomic data.
Conclusions:
- The proposed robust transfer learning method enhances the analysis of high-dimensional genomic data in complex diseases.
- The approach effectively handles data imperfections, offering reliable performance and improved accuracy.
- It holds significant potential for advancing biomarker discovery and risk assessment in cancer research.
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