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Documentation of clinically relevant genomic biomarker allele frequencies in the next-generation FINDbase worldwide database
2020
Human Mutation
FINDbase (http://www.findbase.org) is a comprehensive data resource recording the prevalence of clinically relevant genomic variants in various populations worldwide, such as pathogenic variants underlying genetic disorders as well as pharmacogenomic biomarkers that can guide drug treatment. Here, we report significant new developments and technological advancements in the database architecture, leading to a completely revamped database structure, querying interface, accompanied with
doi:10.1002/humu.24018
pmid:32248568
fatcat:jifzf476fzerpdkuuwp4sj4zua