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LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants., and . Bioinformatics, 31 (21): 3555-3557 (2015)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)LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation., and . Bioinformatics, 34 (5): 887-889 (2018)Polymorphism Interaction Analysis (PIA): a method for investigating complex gene-gene interactions., , , , and . BMC Bioinformatics, (2008)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)A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data., , , , , , , and . BMC Bioinformatics, (2011)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)