Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies

FINDbase (http://www.findbase.org) is a comprehensive data repository that records the prevalence of clinically relevant genomic variants in various populations worldwide, such as pathogenic variants leading mostly to monogenic disorders and pharmacogenomics biomarkers. The database also records the...

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Bibliographic Details
Published in:Nucleic Acids Res
Main Authors: Viennas, Emmanouil, Komianou, Angeliki, Mizzi, Clint, Stojiljkovic, Maja, Mitropoulou, Christina, Muilu, Juha, Vihinen, Mauno, Grypioti, Panagiota, Papadaki, Styliani, Pavlidis, Cristiana, Zukic, Branka, Katsila, Theodora, van der Spek, Peter J., Pavlovic, Sonja, Tzimas, Giannis, Patrinos, George P.
Format: Artigo
Language:Inglês
Published: Oxford University Press 2017
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Database Issue
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5210643/
https://ncbi.nlm.nih.gov/pubmed/27924022
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkw949
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