Article
Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Nucleic acids research - 1 Jan 2014
Papadopoulos Petros, Viennas Emmanouil, Gkantouna Vassiliki, Pavlidis Cristiana, Bartsakoulia Marina, Ioannou Zafeiria-Marina, Ratbi Ilham, Sefiani Abdelaziz, Tsaknakis John, Poulas Konstantinos, Tzimas Giannis, Patrinos George P
Abstract excerpt
FINDbase (http://www.findbase.org) aims to document frequencies of clinically relevant genomic variations, namely causative mutations and pharmacogenomic markers, worldwide. Each database record includes the population, ethnic group or geographical region, the disorder name and the related gene, accompanied by links to any related databases and the genetic variation together with its frequency in that population....
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