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SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes.

, , , , , , , , , , , , , and . Nucleic Acids Research, 34 (Database-Issue): 617-621 (2006)

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SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes., , , , , , , , , and 4 other author(s). Nucleic Acids Research, 34 (Database-Issue): 617-621 (2006)KRLMM: an adaptive genotype calling method for common and low frequency variants., , , , and . BMC Bioinformatics, (2014)SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes., , , , , , , , , and 3 other author(s). Nucleic Acids Research, 32 (Database-Issue): 528-532 (2004)GWASdb: a database for human genetic variants identified by genome-wide association studies., , , , , , , , , and . Nucleic Acids Research, 40 (Database-Issue): 1047-1054 (2012)GWASdb v2: an update database for human genetic variants identified by genome-wide association studies., , , , , , , , , and 1 other author(s). Nucleic Acids Research, 44 (Database-Issue): 869-876 (2016)Viral coinfection analysis using a MinHash toolkit., , , , , , , , , and 3 other author(s). BMC Bioinformatics, 20 (1): 389:1-389:10 (2019)