From post

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed.

 

Другие публикации лиц с тем же именем

A novel computational strategy for DNA methylation imputation using mixture regression model (MRM)., , , и . BMC Bioinform., 21 (1): 552 (2020)A Sparse Regression Method for Group-Wise Feature Selection with False Discovery Rate Control., , , , , и . IEEE ACM Trans. Comput. Biol. Bioinform., 15 (4): 1066-1078 (2018)A generalized kernel machine approach to identify higher-order composite effects in multi-view datasets., , , , и . CoRR, (2020)Multi-View Variational Autoencoder for Missing Value Imputation in Untargeted Metabolomics., , , , , , , , , и 6 other автор(ы). CoRR, (2023)A Staged Approach using Machine Learning and Uncertainty Quantification to Predict the Risk of Hip Fracture., , , , , , , , , и 1 other автор(ы). CoRR, (2024)PCA-based GRS analysis enhances the effectiveness for genetic correlation detection., , , , , , , , , и 8 other автор(ы). Briefings Bioinform., 20 (6): 2291-2298 (2019)CLCLSA: Cross-omics linked embedding with contrastive learning and self attention for integration with incomplete multi-omics data., , , , , , , , и . Comput. Biol. Medicine, (марта 2024)Copy number variation estimation from multiple next-generation sequencing samples., , , , и . BCB, стр. 555-557. ACM, (2012)Identification of genes for complex diseases by integrating multiple types of genomic data., , , и . EMBC, стр. 5541-5544. IEEE, (2012)A generalized sparse regression model with adjustment of pedigree structure for variant detection from next generation sequencing data., , , и . BCB, стр. 191. ACM, (2013)