AI Article Synopsis
- The rise of sequencing and genotyping technologies is making multi-species variation data more accessible, prompting a need to improve how this data is stored and analyzed.
- Ensembl has developed a database and software library that supports the management of large-scale genome variation data and is capable of handling thousands of genomes, benefiting from integration into the Ensembl platform.
- The Ensembl system is open-source and aims to efficiently manage genomic data, and is available for free use on their website.
Article Abstract
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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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882931 | PMC |
| http://dx.doi.org/10.1186/1471-2105-11-238 | DOI Listing |
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