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A database and API for variation, dense genotyping and resequencing data

BACKGROUND: Advances in sequencing and genotyping technologies are leading to the widespread availability of multi-species variation data, dense genotype data and large-scale resequencing projects. The 1000 Genomes Project and similar efforts in other species are challenging the methods previously u...

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Autores principales: Rios, Daniel, McLaren, William M, Chen, Yuan, Birney, Ewan, Stabenau, Arne, Flicek, Paul, Cunningham, Fiona
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882931/
https://www.ncbi.nlm.nih.gov/pubmed/20459810
http://dx.doi.org/10.1186/1471-2105-11-238
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author Rios, Daniel
McLaren, William M
Chen, Yuan
Birney, Ewan
Stabenau, Arne
Flicek, Paul
Cunningham, Fiona
author_facet Rios, Daniel
McLaren, William M
Chen, Yuan
Birney, Ewan
Stabenau, Arne
Flicek, Paul
Cunningham, Fiona
author_sort Rios, Daniel
collection PubMed
description BACKGROUND: Advances in sequencing and genotyping technologies are leading to the widespread availability of multi-species variation data, dense genotype data and large-scale resequencing projects. The 1000 Genomes Project and similar efforts in other species are challenging the methods previously used for storage and manipulation of such data necessitating the redesign of existing genome-wide bioinformatics resources. RESULTS: Ensembl has created a database and software library to support data storage, analysis and access to the existing and emerging variation data from large mammalian and vertebrate genomes. These tools scale to thousands of individual genome sequences and are integrated into the Ensembl infrastructure for genome annotation and visualisation. The database and software system is easily expanded to integrate both public and non-public data sources in the context of an Ensembl software installation and is already being used outside of the Ensembl project in a number of database and application environments. CONCLUSIONS: Ensembl's powerful, flexible and open source infrastructure for the management of variation, genotyping and resequencing data is freely available at http://www.ensembl.org.
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spelling pubmed-28829312010-06-10 A database and API for variation, dense genotyping and resequencing data Rios, Daniel McLaren, William M Chen, Yuan Birney, Ewan Stabenau, Arne Flicek, Paul Cunningham, Fiona BMC Bioinformatics Software BACKGROUND: Advances in sequencing and genotyping technologies are leading to the widespread availability of multi-species variation data, dense genotype data and large-scale resequencing projects. The 1000 Genomes Project and similar efforts in other species are challenging the methods previously used for storage and manipulation of such data necessitating the redesign of existing genome-wide bioinformatics resources. RESULTS: Ensembl has created a database and software library to support data storage, analysis and access to the existing and emerging variation data from large mammalian and vertebrate genomes. These tools scale to thousands of individual genome sequences and are integrated into the Ensembl infrastructure for genome annotation and visualisation. The database and software system is easily expanded to integrate both public and non-public data sources in the context of an Ensembl software installation and is already being used outside of the Ensembl project in a number of database and application environments. CONCLUSIONS: Ensembl's powerful, flexible and open source infrastructure for the management of variation, genotyping and resequencing data is freely available at http://www.ensembl.org. BioMed Central 2010-05-11 /pmc/articles/PMC2882931/ /pubmed/20459810 http://dx.doi.org/10.1186/1471-2105-11-238 Text en Copyright ©2010 Rios et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software
Rios, Daniel
McLaren, William M
Chen, Yuan
Birney, Ewan
Stabenau, Arne
Flicek, Paul
Cunningham, Fiona
A database and API for variation, dense genotyping and resequencing data
title A database and API for variation, dense genotyping and resequencing data
title_full A database and API for variation, dense genotyping and resequencing data
title_fullStr A database and API for variation, dense genotyping and resequencing data
title_full_unstemmed A database and API for variation, dense genotyping and resequencing data
title_short A database and API for variation, dense genotyping and resequencing data
title_sort database and api for variation, dense genotyping and resequencing data
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882931/
https://www.ncbi.nlm.nih.gov/pubmed/20459810
http://dx.doi.org/10.1186/1471-2105-11-238
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