| 词条 | FINDbase |
| 释义 |
}}{{infobox biodatabase |title = FINDbase |logo = |description =genetic variation allele frequencies. |scope = |organism = |center = University of Patras, Patras, Greece. |laboratory = Department of Pharmacy, School of Health Sciences, Faculty of Engineering |author = Marianthi Georgitsi |citation = Georgitsi & al. (2011)[1] |released = 2006 |standard = |format = |url = http://www.findbase.org |download = |webservice = |sql = |sparql = |webapp = |standalone = |license = |versioning = |frequency = |curation = |bookmark = |version= }}The Frequency of INherited Disorders database (FINDbase) is a database of frequencies of causative genetic variations worldwide.[1][2] FINDbase was founded in 2006 to be a relational database for these frequencies of causative genetic variations of inherited genetic disorders, as well as pharmacogenetic markers. Out of all the national/ethnic mutation databases (NEMDBs), FINDbase has the most content and since all the entries are collected from various populations worldwide, it is seen as a great resource for population-specific information.[3] See also
References1. ^1 {{cite journal |last=Georgitsi|first=Marianthi|authorlink=|author2=Viennas Emmanouil |author3=Antoniou Dimitris I |author4=Gkantouna Vassiliki |author5=van Baal Sjozef |author6=Petricoin Emanuel F |author7=Poulas Konstantinos |author8=Tzimas Giannis |author9=Patrinos George P |date=Jan 2011|title=FINDbase: a worldwide database for genetic variation allele frequencies updated|journal = Nucleic Acids Res.|volume=39|issue=Database issue|pages=D926–32| issn = | pmid = 21113021|doi = 10.1093/nar/gkq1236| bibcode = | oclc =| id = | url = | pmc =3013745 | format = | accessdate = | laysummary = | laysource = | laydate = | quote = }} 2. ^{{cite journal |last=Papadopoulos |first=Petros |author2=Emmanouil Viennas |author3=Vassiliki Gkantouna |author4=Cristiana Pavlidis |author5=Marina Bartsakoulia |author6=Zafeiria-Marina Ioannou |author7=Ilham Ratbi |author8=Abdelaziz Sefiani |author9=John Tsaknakis |author10=Konstantinos Poulas |author11=Giannis Tzimas |author12=George P. Patrinos |date=Jan 2014 |title=Developments in FINDbase database for clinically relevant genomic variation allele frequencies |journal=Nucleic Acids Res. |volume=42 |issue=Database issue |pages=D1020–6 |pmid=24234438 |doi=10.1093/nar/gkt1125 |pmc=3964978}} 3. ^{{Cite book|title = Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase) - Springer|journal = |volume = 1015|pages = 321–336|publisher = Humana Press|date = 2013-01-01|isbn = 978-1-62703-434-0|series = Methods in Molecular Biology|doi = 10.1007/978-1-62703-435-7_21|pmid = 23824866|editor-first = Federico|editor-last = Innocenti|editor-first2 = Ron H. N. van|editor-last2 = Schaik|chapter = Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase)|last1 = Georgitsi|first1 = M.|last2 = Patrinos|first2 = G. P.}} External links
2 : Biological databases|Population genetics |
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