Misplaced Pages

FINDbase

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
This article has multiple issues. Please help improve it or discuss these issues on the talk page. (Learn how and when to remove these messages)
This article may contain excessive or inappropriate references to self-published sources. Please help improve it by removing references to unreliable sources where they are used inappropriately. (August 2011) (Learn how and when to remove this message)
This article relies excessively on references to primary sources. Please improve this article by adding secondary or tertiary sources.
Find sources: "FINDbase" – news · newspapers · books · scholar · JSTOR (August 2011) (Learn how and when to remove this message)
The topic of this article may not meet Misplaced Pages's general notability guideline. Please help to demonstrate the notability of the topic by citing reliable secondary sources that are independent of the topic and provide significant coverage of it beyond a mere trivial mention. If notability cannot be shown, the article is likely to be merged, redirected, or deleted.
Find sources: "FINDbase" – news · newspapers · books · scholar · JSTOR (August 2011) (Learn how and when to remove this message)
(Learn how and when to remove this message)
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)
Release date2006
Access
Websitehttp://www.findbase.org

The Frequency of INherited Disorders database (FINDbase) is a database of frequencies of causative genetic variations worldwide. 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.

See also

References

  1. ^ 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.
  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.

External links


Stub icon

This Biological database-related article is a stub. You can help Misplaced Pages by expanding it.

Categories: