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    Area of Science:

    • Biomedical data analysis
    • Computational biology
    • Machine learning in genomics

    Background:

    • Limited omics data hinders accurate predictive model design in biomedicine.
    • Omics data often share underlying biological pathways and disease mechanisms.
    • Leveraging data from relevant source domains can improve predictions in data-limited target domains.

    Purpose of the Study:

    • To develop Bayesian transfer learning methods for next-generation sequencing (NGS) data analysis.
    • To improve prediction accuracy and reliability in target domains with scarce labeled data.
    • To propose an Optimal Bayesian Transfer Learning (OBTL) classifier.

    Main Methods:

    • Formulating transfer learning within a fully Bayesian framework.
    • Defining relatedness via joint prior distributions of source and target domain model parameters.
    • Utilizing the Negative Binomial model for overdispersed RNA-seq count data and proposing the OBTL classifier to minimize expected classification error.

    Main Results:

    • The proposed Optimal Bayesian Transfer Learning (OBTL) classifier effectively transfers knowledge from source to target domains.
    • The OBTL classifier demonstrates improved predictive performance on both synthetic and real-world cancer genomics data.
    • Bayesian transfer learning provides a robust approach for omics data analysis with limited sample sizes.

    Conclusions:

    • Bayesian transfer learning offers a powerful framework for enhancing predictive modeling with omics data.
    • The OBTL classifier effectively addresses challenges posed by data scarcity and overdispersion in RNA-seq data.
    • This approach holds significant potential for advancing precision medicine and biomedical research through improved data utilization.