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Sequencing genes in silico using single nucleotide polymorphisms
BACKGROUND: The advent of high throughput sequencing technology has enabled the 1000 Genomes Project Pilot 3 to generate complete sequence data for more than 906 genes and 8,140 exons representing 697 subjects. The 1000 Genomes database provides a critical opportunity for further interpreting diseas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283449/ https://www.ncbi.nlm.nih.gov/pubmed/22289434 http://dx.doi.org/10.1186/1471-2156-13-6 |
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author | Zhang, Xinyi Cindy Zhang, Bo Li, Shuying Sue Huang, Xin Hansen, John A Zhao, Lue Ping |
author_facet | Zhang, Xinyi Cindy Zhang, Bo Li, Shuying Sue Huang, Xin Hansen, John A Zhao, Lue Ping |
author_sort | Zhang, Xinyi Cindy |
collection | PubMed |
description | BACKGROUND: The advent of high throughput sequencing technology has enabled the 1000 Genomes Project Pilot 3 to generate complete sequence data for more than 906 genes and 8,140 exons representing 697 subjects. The 1000 Genomes database provides a critical opportunity for further interpreting disease associations with single nucleotide polymorphisms (SNPs) discovered from genetic association studies. Currently, direct sequencing of candidate genes or regions on a large number of subjects remains both cost- and time-prohibitive. RESULTS: To accelerate the translation from discovery to functional studies, we propose an in silico gene sequencing method (ISS), which predicts phased sequences of intragenic regions, using SNPs. The key underlying idea of our method is to infer diploid sequences (a pair of phased sequences/alleles) at every functional locus utilizing the deep sequencing data from the 1000 Genomes Project and SNP data from the HapMap Project, and to build prediction models using flanking SNPs. Using this method, we have developed a database of prediction models for 611 known genes. Sequence prediction accuracy for these genes is 96.26% on average (ranges 79%-100%). This database of prediction models can be enhanced and scaled up to include new genes as the 1000 Genomes Project sequences additional genes on additional individuals. Applying our predictive model for the KCNJ11 gene to the Wellcome Trust Case Control Consortium (WTCCC) Type 2 diabetes cohort, we demonstrate how the prediction of phased sequences inferred from GWAS SNP genotype data can be used to facilitate interpretation and identify a probable functional mechanism such as protein changes. CONCLUSIONS: Prior to the general availability of routine sequencing of all subjects, the ISS method proposed here provides a time- and cost-effective approach to broadening the characterization of disease associated SNPs and regions, and facilitating the prioritization of candidate genes for more detailed functional and mechanistic studies. |
format | Online Article Text |
id | pubmed-3283449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32834492012-02-22 Sequencing genes in silico using single nucleotide polymorphisms Zhang, Xinyi Cindy Zhang, Bo Li, Shuying Sue Huang, Xin Hansen, John A Zhao, Lue Ping BMC Genet Research Article BACKGROUND: The advent of high throughput sequencing technology has enabled the 1000 Genomes Project Pilot 3 to generate complete sequence data for more than 906 genes and 8,140 exons representing 697 subjects. The 1000 Genomes database provides a critical opportunity for further interpreting disease associations with single nucleotide polymorphisms (SNPs) discovered from genetic association studies. Currently, direct sequencing of candidate genes or regions on a large number of subjects remains both cost- and time-prohibitive. RESULTS: To accelerate the translation from discovery to functional studies, we propose an in silico gene sequencing method (ISS), which predicts phased sequences of intragenic regions, using SNPs. The key underlying idea of our method is to infer diploid sequences (a pair of phased sequences/alleles) at every functional locus utilizing the deep sequencing data from the 1000 Genomes Project and SNP data from the HapMap Project, and to build prediction models using flanking SNPs. Using this method, we have developed a database of prediction models for 611 known genes. Sequence prediction accuracy for these genes is 96.26% on average (ranges 79%-100%). This database of prediction models can be enhanced and scaled up to include new genes as the 1000 Genomes Project sequences additional genes on additional individuals. Applying our predictive model for the KCNJ11 gene to the Wellcome Trust Case Control Consortium (WTCCC) Type 2 diabetes cohort, we demonstrate how the prediction of phased sequences inferred from GWAS SNP genotype data can be used to facilitate interpretation and identify a probable functional mechanism such as protein changes. CONCLUSIONS: Prior to the general availability of routine sequencing of all subjects, the ISS method proposed here provides a time- and cost-effective approach to broadening the characterization of disease associated SNPs and regions, and facilitating the prioritization of candidate genes for more detailed functional and mechanistic studies. BioMed Central 2012-01-30 /pmc/articles/PMC3283449/ /pubmed/22289434 http://dx.doi.org/10.1186/1471-2156-13-6 Text en Copyright ©2012 Zhang 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 | Research Article Zhang, Xinyi Cindy Zhang, Bo Li, Shuying Sue Huang, Xin Hansen, John A Zhao, Lue Ping Sequencing genes in silico using single nucleotide polymorphisms |
title | Sequencing genes in silico using single nucleotide polymorphisms |
title_full | Sequencing genes in silico using single nucleotide polymorphisms |
title_fullStr | Sequencing genes in silico using single nucleotide polymorphisms |
title_full_unstemmed | Sequencing genes in silico using single nucleotide polymorphisms |
title_short | Sequencing genes in silico using single nucleotide polymorphisms |
title_sort | sequencing genes in silico using single nucleotide polymorphisms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283449/ https://www.ncbi.nlm.nih.gov/pubmed/22289434 http://dx.doi.org/10.1186/1471-2156-13-6 |
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