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}}The '''Frequency of INherited Disorders''' database ('''FINDbase''') is a database of frequencies of causative genetic variations worldwide.<ref name="pmid21113021">{{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|publisher= |location = England| issn = | pmid = 21113021|doi = 10.1093/nar/gkq1236| bibcode = | oclc =| id = | url = | pmc =3013745 | format = | accessdate = | laysummary = | laysource = | laydate = | quote = }}</ref><ref name="pmid24234438">{{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 |location=England |pmid=24234438 |doi=10.1093/nar/gkt1125 |pmc=3964978}}</ref> '''FINDbase''' was founded in 2006 to be a [[relational database]] for these frequencies of causative genetic variations of inherited genetic disorders, as well as [[pharmacogenetics|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.<ref>{{Cite book|title = Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase) - Springer|url = https://link.springer.com/protocol/10.1007%2F978-1-62703-435-7_21|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|editor-first = Federico|editor-last = Innocenti|editor-first2 = Ron H. N. van|editor-last2 = Schaik}}</ref>
}}The '''Frequency of INherited Disorders''' database ('''FINDbase''') is a database of frequencies of causative genetic variations worldwide.<ref name="pmid21113021">{{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 = }}</ref><ref name="pmid24234438">{{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}}</ref> '''FINDbase''' was founded in 2006 to be a [[relational database]] for these frequencies of causative genetic variations of inherited genetic disorders, as well as [[pharmacogenetics|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.<ref>{{Cite book|title = Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase) - Springer|journal = Methods in Molecular Biology (Clifton, N.j.)|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.}}</ref>


==See also==
==See also==

Revision as of 13:30, 28 January 2019

FINDbase
Content
Descriptiongenetic variation allele frequencies.
Contact
Research centerUniversity of Patras, Patras, Greece.
LaboratoryDepartment of Pharmacy, School of Health Sciences, Faculty of Engineering
AuthorsMarianthi Georgitsi
Primary citationGeorgitsi & al. (2011)[1]
Release date2006
Access
Websitehttp://www.findbase.org

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

References

  1. ^ a b Georgitsi, Marianthi; Viennas Emmanouil; Antoniou Dimitris I; Gkantouna Vassiliki; van Baal Sjozef; Petricoin Emanuel F; Poulas Konstantinos; Tzimas Giannis; Patrinos George P (Jan 2011). "FINDbase: a worldwide database for genetic variation allele frequencies updated". Nucleic Acids Res. 39 (Database issue): D926–32. doi:10.1093/nar/gkq1236. PMC 3013745. PMID 21113021. {{cite journal}}: Cite has empty unknown parameters: |laydate=, |laysource=, and |laysummary= (help)
  2. ^ Papadopoulos, Petros; Emmanouil Viennas; Vassiliki Gkantouna; Cristiana Pavlidis; Marina Bartsakoulia; Zafeiria-Marina Ioannou; Ilham Ratbi; Abdelaziz Sefiani; John Tsaknakis; Konstantinos Poulas; Giannis Tzimas; George P. Patrinos (Jan 2014). "Developments in FINDbase database for clinically relevant genomic variation allele frequencies". Nucleic Acids Res. 42 (Database issue): D1020–6. doi:10.1093/nar/gkt1125. PMC 3964978. PMID 24234438.
  3. ^ Georgitsi, M.; Patrinos, G. P. (2013-01-01). "Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase)". In Innocenti, Federico; Schaik, Ron H. N. van (eds.). Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase) - Springer. Methods in Molecular Biology. Vol. 1015. Humana Press. pp. 321–336. doi:10.1007/978-1-62703-435-7_21. ISBN 978-1-62703-434-0. PMID 23824866. {{cite book}}: |journal= ignored (help)


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