Machine Learning: Develop, benchmark, and validate machine learning models on high-dimensional genetic and molecular data for tasks such as variant effect prediction, patient stratification, and biomarker or treatment-response prediction; apply rigorous cross-validation, control for batch and ancestry confounding, and use interpretability methods to translate models into testable biological hypotheses (e.g., scikit-learn, XGBoost, PyTorch, SHAP). Multi-Omics Data Integration: Integrate genetic datasets with other omics layers, including transcriptomic (bulk and single-cell RNA-seq), epigenomic, proteomic (e.g., OLINK, mass spectrometry), and spatial data, to provide comprehensive insights into gene function and disease biology (e.g., DESeq2, limma, Seurat, scanpy).