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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...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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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. |
format | Text |
id | pubmed-3013653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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