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CRAVAT: cancer-related analysis of variants toolkit., , , , , , , , and . Bioinformatics, 29 (5): 647-648 (2013)Erratum: Identifying mutation specific cancer pathways using a structurally resolved protein interaction network., , and . PSB, page 634. (2018)Computational KIR copy number discovery reveals interaction between inhibitory receptor burden and survival., , , , , and . PSB, page 148-159. (2019)MODBASE, a database of annotated comparative protein structure models and associated resources., , , , , , , , , and 2 other author(s). Nucleic Acids Research, 37 (Database-Issue): 347-354 (2009)A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing., , , , , , , , , and 2 other author(s). PLoS Computational Biology, (2014)Identifying Mutation Specific Cancer Pathways Using a Structurally Resolved Protein Interaction Network., , and . Pacific Symposium on Biocomputing, page 84-95. (2015)Extracting allelic read counts from 250, 000 human sequencing runs in Sequence Read Archive., , , and . PSB, page 196-207. (2019)CHASM and SNVBox: toolkit for detecting biologically important single nucleotide mutations in cancer., , , , , and . Bioinformatics, 27 (15): 2147-2148 (2011)Rare variant phasing using paired tumor: normal sequence data., , , and . BMC Bioinformatics, 20 (1): 265:1-265:11 (2019)