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Identification of deleterious synonymous variants in human genomes., , , , and . Bioinform., 31 (5): 799 (2015)VARiD: A variation detection framework for color-space and letter-space platforms., , , and . Bioinform., 26 (12): 343-349 (2010)Identifying Clinical Terms in Free-Text Notes Using Ontology-Guided Machine Learning., , , and . RECOMB, volume 11467 of Lecture Notes in Computer Science, page 19-34. Springer, (2019)Centroid-based Deep Metric Learning for Speaker Recognition., , , , and . ICASSP, page 3652-3656. IEEE, (2019)Session Introduction., , , and . Pacific Symposium on Biocomputing, page 1-2. World Scientific, (2008)FRESCO: Flexible Alignment with Rectangle Scoring Schemes., and . Pacific Symposium on Biocomputing, page 3-14. World Scientific, (2008)ASDB: database of alternatively spliced genes., , , , and . Nucleic Acids Res., 28 (1): 296-297 (2000)Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources., , , , , , , , , and 59 other author(s). Nucleic Acids Res., 47 (Database-Issue): D1018-D1027 (2019): Navigating large collections of text notes in electronic health records for clinical chart review., , , and . IEEE Trans. Vis. Comput. Graph., 29 (1): 1244-1254 (2023)PhenoPad: Building AI enabled note-taking interfaces for patient encounters., , , , , , , , and . npj Digit. Medicine, (2022)