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A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing., , , , , , , , , and 2 other author(s). PLoS Computational Biology, (2014)A novel approach for selecting combination clinical markers of pathology applied to a large retrospective cohort of surgically resected pancreatic cysts., , , , , , , , , and 26 other author(s). JAMIA, 24 (1): 145-152 (2017)Using bioinformatics to predict the functional impact of SNVs., and . Bioinformatics, 27 (4): 441-448 (2011)Session Introduction., , , , and . Pacific Symposium on Biocomputing, page 103-110. World Scientific Publishing, (2013)Workshop Introduction., , , and . Pacific Symposium on Biocomputing, page 364-368. World Scientific Publishing, (2011)Protein Interactions and Disease Phenotypes in the ABC Transporter Superfamily., , and . Pacific Symposium on Biocomputing, page 51-63. World Scientific, (2007)LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources., , , , , , , and . Bioinformatics, 21 (12): 2814-2820 (2005)CHASM and SNVBox: toolkit for detecting biologically important single nucleotide mutations in cancer., , , , , and . Bioinformatics, 27 (15): 2147-2148 (2011)Improving Functional Annotation of Non-Synonomous SNPs with Information Theory., , and . Pacific Symposium on Biocomputing, World Scientific, (2005)MODBASE: a database of annotated comparative protein structure models and associated resources., , , , , , , , , and 4 other author(s). Nucleic Acids Research, 34 (Database-Issue): 291-295 (2006)