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Indian genetic disease database

Indians, representing about one-sixth of the world population, consist of several thousands of endogamous groups with strong potential for excess of recessive diseases. However, no database is available on Indian population with comprehensive information on the diseases common in the country. To add...

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Detalles Bibliográficos
Autores principales: Pradhan, Sanchari, Sengupta, Mainak, Dutta, Anirban, Bhattacharyya, Kausik, Bag, Sumit K., Dutta, Chitra, Ray, Kunal
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013653/
https://www.ncbi.nlm.nih.gov/pubmed/21037256
http://dx.doi.org/10.1093/nar/gkq1025
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author Pradhan, Sanchari
Sengupta, Mainak
Dutta, Anirban
Bhattacharyya, Kausik
Bag, Sumit K.
Dutta, Chitra
Ray, Kunal
author_facet Pradhan, Sanchari
Sengupta, Mainak
Dutta, Anirban
Bhattacharyya, Kausik
Bag, Sumit K.
Dutta, Chitra
Ray, Kunal
author_sort Pradhan, Sanchari
collection PubMed
description Indians, representing about one-sixth of the world population, consist of several thousands of endogamous groups with strong potential for excess of recessive diseases. However, no database is available on Indian population with comprehensive information on the diseases common in the country. To address this issue, we present Indian Genetic Disease Database (IGDD) release 1.0 (http://www.igdd.iicb.res.in)—an integrated and curated repository of growing number of mutation data on common genetic diseases afflicting the Indian populations. Currently the database covers 52 diseases with information on 5760 individuals carrying the mutant alleles of causal genes. Information on locus heterogeneity, type of mutation, clinical and biochemical data, geographical location and common mutations are furnished based on published literature. The database is currently designed to work best with Internet Explorer 8 (optimal resolution 1440 × 900) and it can be searched based on disease of interest, causal gene, type of mutation and geographical location of the patients or carriers. Provisions have been made for deposition of new data and logistics for regular updation of the database. The IGDD web portal, planned to be made freely available, contains user-friendly interfaces and is expected to be highly useful to the geneticists, clinicians, biologists and patient support groups of various genetic diseases.
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spelling pubmed-30136532011-01-03 Indian genetic disease database Pradhan, Sanchari Sengupta, Mainak Dutta, Anirban Bhattacharyya, Kausik Bag, Sumit K. Dutta, Chitra Ray, Kunal Nucleic Acids Res Articles Indians, representing about one-sixth of the world population, consist of several thousands of endogamous groups with strong potential for excess of recessive diseases. However, no database is available on Indian population with comprehensive information on the diseases common in the country. To address this issue, we present Indian Genetic Disease Database (IGDD) release 1.0 (http://www.igdd.iicb.res.in)—an integrated and curated repository of growing number of mutation data on common genetic diseases afflicting the Indian populations. Currently the database covers 52 diseases with information on 5760 individuals carrying the mutant alleles of causal genes. Information on locus heterogeneity, type of mutation, clinical and biochemical data, geographical location and common mutations are furnished based on published literature. The database is currently designed to work best with Internet Explorer 8 (optimal resolution 1440 × 900) and it can be searched based on disease of interest, causal gene, type of mutation and geographical location of the patients or carriers. Provisions have been made for deposition of new data and logistics for regular updation of the database. The IGDD web portal, planned to be made freely available, contains user-friendly interfaces and is expected to be highly useful to the geneticists, clinicians, biologists and patient support groups of various genetic diseases. Oxford University Press 2011-01 2010-10-30 /pmc/articles/PMC3013653/ /pubmed/21037256 http://dx.doi.org/10.1093/nar/gkq1025 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Pradhan, Sanchari
Sengupta, Mainak
Dutta, Anirban
Bhattacharyya, Kausik
Bag, Sumit K.
Dutta, Chitra
Ray, Kunal
Indian genetic disease database
title Indian genetic disease database
title_full Indian genetic disease database
title_fullStr Indian genetic disease database
title_full_unstemmed Indian genetic disease database
title_short Indian genetic disease database
title_sort indian genetic disease database
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013653/
https://www.ncbi.nlm.nih.gov/pubmed/21037256
http://dx.doi.org/10.1093/nar/gkq1025
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