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ENGINES: exploring single nucleotide variation in entire human genomes
BACKGROUND: Next generation ultra-sequencing technologies are starting to produce extensive quantities of data from entire human genome or exome sequences, and therefore new software is needed to present and analyse this vast amount of information. The 1000 Genomes project has recently released raw...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107182/ https://www.ncbi.nlm.nih.gov/pubmed/21504571 http://dx.doi.org/10.1186/1471-2105-12-105 |
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author | Amigo, Jorge Salas, Antonio Phillips, Christopher |
author_facet | Amigo, Jorge Salas, Antonio Phillips, Christopher |
author_sort | Amigo, Jorge |
collection | PubMed |
description | BACKGROUND: Next generation ultra-sequencing technologies are starting to produce extensive quantities of data from entire human genome or exome sequences, and therefore new software is needed to present and analyse this vast amount of information. The 1000 Genomes project has recently released raw data for 629 complete genomes representing several human populations through their Phase I interim analysis and, although there are certain public tools available that allow exploration of these genomes, to date there is no tool that permits comprehensive population analysis of the variation catalogued by such data. DESCRIPTION: We have developed a genetic variant site explorer able to retrieve data for Single Nucleotide Variation (SNVs), population by population, from entire genomes without compromising future scalability and agility. ENGINES (ENtire Genome INterface for Exploring SNVs) uses data from the 1000 Genomes Phase I to demonstrate its capacity to handle large amounts of genetic variation (>7.3 billion genotypes and 28 million SNVs), as well as deriving summary statistics of interest for medical and population genetics applications. The whole dataset is pre-processed and summarized into a data mart accessible through a web interface. The query system allows the combination and comparison of each available population sample, while searching by rs-number list, chromosome region, or genes of interest. Frequency and F(ST )filters are available to further refine queries, while results can be visually compared with other large-scale Single Nucleotide Polymorphism (SNP) repositories such as HapMap or Perlegen. CONCLUSIONS: ENGINES is capable of accessing large-scale variation data repositories in a fast and comprehensive manner. It allows quick browsing of whole genome variation, while providing statistical information for each variant site such as allele frequency, heterozygosity or F(ST )values for genetic differentiation. Access to the data mart generating scripts and to the web interface is granted from http://spsmart.cesga.es/engines.php |
format | Online Article Text |
id | pubmed-3107182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31071822011-06-03 ENGINES: exploring single nucleotide variation in entire human genomes Amigo, Jorge Salas, Antonio Phillips, Christopher BMC Bioinformatics Database BACKGROUND: Next generation ultra-sequencing technologies are starting to produce extensive quantities of data from entire human genome or exome sequences, and therefore new software is needed to present and analyse this vast amount of information. The 1000 Genomes project has recently released raw data for 629 complete genomes representing several human populations through their Phase I interim analysis and, although there are certain public tools available that allow exploration of these genomes, to date there is no tool that permits comprehensive population analysis of the variation catalogued by such data. DESCRIPTION: We have developed a genetic variant site explorer able to retrieve data for Single Nucleotide Variation (SNVs), population by population, from entire genomes without compromising future scalability and agility. ENGINES (ENtire Genome INterface for Exploring SNVs) uses data from the 1000 Genomes Phase I to demonstrate its capacity to handle large amounts of genetic variation (>7.3 billion genotypes and 28 million SNVs), as well as deriving summary statistics of interest for medical and population genetics applications. The whole dataset is pre-processed and summarized into a data mart accessible through a web interface. The query system allows the combination and comparison of each available population sample, while searching by rs-number list, chromosome region, or genes of interest. Frequency and F(ST )filters are available to further refine queries, while results can be visually compared with other large-scale Single Nucleotide Polymorphism (SNP) repositories such as HapMap or Perlegen. CONCLUSIONS: ENGINES is capable of accessing large-scale variation data repositories in a fast and comprehensive manner. It allows quick browsing of whole genome variation, while providing statistical information for each variant site such as allele frequency, heterozygosity or F(ST )values for genetic differentiation. Access to the data mart generating scripts and to the web interface is granted from http://spsmart.cesga.es/engines.php BioMed Central 2011-04-19 /pmc/articles/PMC3107182/ /pubmed/21504571 http://dx.doi.org/10.1186/1471-2105-12-105 Text en Copyright ©2011 Amigo 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 | Database Amigo, Jorge Salas, Antonio Phillips, Christopher ENGINES: exploring single nucleotide variation in entire human genomes |
title | ENGINES: exploring single nucleotide variation in entire human genomes |
title_full | ENGINES: exploring single nucleotide variation in entire human genomes |
title_fullStr | ENGINES: exploring single nucleotide variation in entire human genomes |
title_full_unstemmed | ENGINES: exploring single nucleotide variation in entire human genomes |
title_short | ENGINES: exploring single nucleotide variation in entire human genomes |
title_sort | engines: exploring single nucleotide variation in entire human genomes |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107182/ https://www.ncbi.nlm.nih.gov/pubmed/21504571 http://dx.doi.org/10.1186/1471-2105-12-105 |
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