Wen-Yun Yang, Ph.D.
Affiliations: | 2013 | Computer Science 0201 | University of California, Los Angeles, Los Angeles, CA |
Area:
bioinformatics; computational biology; machine learningGoogle:
"Wen-Yun Yang"Parents
Sign in to add mentorEleazar Eskin | grad student | 2013 | UCLA | |
(Efficient Probabilistic Model Based Approaches for Analysis of Human Genomic Data.) |
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Publications
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Lippert C, Sabatini R, Maher MC, et al. (2017) Identification of individuals by trait prediction using whole-genome sequencing data. Proceedings of the National Academy of Sciences of the United States of America |
Sul JH, Bilow M, Yang WY, et al. (2016) Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models. Plos Genetics. 12: e1005849 |
Hormozdiari F, Kichaev G, Yang WY, et al. (2015) Identification of causal genes for complex traits. Bioinformatics (Oxford, England). 31: i206-i213 |
Zhang Y, Yang J, Zhang J, et al. (2015) Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations. Annals of the Rheumatic Diseases |
Yang WY, Hormozdiari F, Eskin E, et al. (2015) A spatial haplotype copying model with applications to genotype imputation. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 22: 451-62 |
Yang WY, Platt A, Chiang CW, et al. (2014) Spatial localization of recent ancestors for admixed individuals. G3 (Bethesda, Md.). 4: 2505-18 |
Kichaev G, Yang WY, Lindstrom S, et al. (2014) Integrating functional data to prioritize causal variants in statistical fine-mapping studies. Plos Genetics. 10: e1004722 |
Yang WY, Hormozdiari F, Eskin E, et al. (2014) A spatial-aware haplotype copying model with applications to genotype imputation Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8394: 371-384 |
Yang WY, Hormozdiari F, Wang Z, et al. (2013) Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data. Bioinformatics (Oxford, England). 29: 2245-52 |
Wang Z, Hormozdiari F, Yang WY, et al. (2013) CNVeM: copy number variation detection using uncertainty of read mapping. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 20: 224-36 |