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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Dades bibliogràfiques
Publicat a:Nucleic Acids Res
Autors principals: 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
Idioma:Inglês
Publicat: Oxford University Press 2017
Matèries:
Database Issue
Accés en línia: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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