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SNP haplotype tagging from DNA pools of two individuals

BACKGROUND: DNA pooling is a technique to reduce genotyping effort while incurring only minor losses in accuracy of allele frequency estimates for single nucleotide polymorphism (SNP) markers. RESULTS: We present an algorithm for reconstructing haplotypes (alleles for multiple SNPs on same chromosom...

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Autores principales: Hoh, Josephine, Matsuda, Fumihiko, Peng, Xu, Markovic, Daniela, Lathrop, Mark G, Ott, Jurg
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156884/
https://www.ncbi.nlm.nih.gov/pubmed/12709267
http://dx.doi.org/10.1186/1471-2105-4-14
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author Hoh, Josephine
Matsuda, Fumihiko
Peng, Xu
Markovic, Daniela
Lathrop, Mark G
Ott, Jurg
author_facet Hoh, Josephine
Matsuda, Fumihiko
Peng, Xu
Markovic, Daniela
Lathrop, Mark G
Ott, Jurg
author_sort Hoh, Josephine
collection PubMed
description BACKGROUND: DNA pooling is a technique to reduce genotyping effort while incurring only minor losses in accuracy of allele frequency estimates for single nucleotide polymorphism (SNP) markers. RESULTS: We present an algorithm for reconstructing haplotypes (alleles for multiple SNPs on same chromosome) from pools of two individual DNAs, in which Hardy-Weinberg equilibrium conditions or other assumptions are not required. The program outputs, in addition to inferred haplotypes, a minimal number of haplotype-tagging SNPs that are identified after an exhaustive search procedure. CONCLUSION: Our method and algorithms lead to a significant reduction in genotyping effort, for example, in case-control disease association studies while maintaining the possibility of reconstructing haplotypes under very general conditions.
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spelling pubmed-1568842003-06-07 SNP haplotype tagging from DNA pools of two individuals Hoh, Josephine Matsuda, Fumihiko Peng, Xu Markovic, Daniela Lathrop, Mark G Ott, Jurg BMC Bioinformatics Methodology Article BACKGROUND: DNA pooling is a technique to reduce genotyping effort while incurring only minor losses in accuracy of allele frequency estimates for single nucleotide polymorphism (SNP) markers. RESULTS: We present an algorithm for reconstructing haplotypes (alleles for multiple SNPs on same chromosome) from pools of two individual DNAs, in which Hardy-Weinberg equilibrium conditions or other assumptions are not required. The program outputs, in addition to inferred haplotypes, a minimal number of haplotype-tagging SNPs that are identified after an exhaustive search procedure. CONCLUSION: Our method and algorithms lead to a significant reduction in genotyping effort, for example, in case-control disease association studies while maintaining the possibility of reconstructing haplotypes under very general conditions. BioMed Central 2003-04-22 /pmc/articles/PMC156884/ /pubmed/12709267 http://dx.doi.org/10.1186/1471-2105-4-14 Text en Copyright © 2003 Hoh et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Methodology Article
Hoh, Josephine
Matsuda, Fumihiko
Peng, Xu
Markovic, Daniela
Lathrop, Mark G
Ott, Jurg
SNP haplotype tagging from DNA pools of two individuals
title SNP haplotype tagging from DNA pools of two individuals
title_full SNP haplotype tagging from DNA pools of two individuals
title_fullStr SNP haplotype tagging from DNA pools of two individuals
title_full_unstemmed SNP haplotype tagging from DNA pools of two individuals
title_short SNP haplotype tagging from DNA pools of two individuals
title_sort snp haplotype tagging from dna pools of two individuals
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156884/
https://www.ncbi.nlm.nih.gov/pubmed/12709267
http://dx.doi.org/10.1186/1471-2105-4-14
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