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Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population

BACKGROUND: The International Hapmap project serves as a valuable resource for human genome variation data, however its applicability to other populations has yet to be exhaustively investigated. In this paper, we use high density genotyping chips and resequencing strategies to compare the Singapore...

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Autores principales: Andiappan, Anand Kumar, Anantharaman, Ramani, Nilkanth, Pallavi Parate, Wang, De Yun, Chew, Fook Tim
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877651/
https://www.ncbi.nlm.nih.gov/pubmed/20459637
http://dx.doi.org/10.1186/1471-2156-11-36
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author Andiappan, Anand Kumar
Anantharaman, Ramani
Nilkanth, Pallavi Parate
Wang, De Yun
Chew, Fook Tim
author_facet Andiappan, Anand Kumar
Anantharaman, Ramani
Nilkanth, Pallavi Parate
Wang, De Yun
Chew, Fook Tim
author_sort Andiappan, Anand Kumar
collection PubMed
description BACKGROUND: The International Hapmap project serves as a valuable resource for human genome variation data, however its applicability to other populations has yet to be exhaustively investigated. In this paper, we use high density genotyping chips and resequencing strategies to compare the Singapore Chinese population with the Hapmap populations. First we compared 1028 and 114 unrelated Singapore Chinese samples genotyped using the Illumina Human Hapmap 550 k chip and Affymetrix 500 k array respectively against the 270 samples from Hapmap. Secondly, data from 20 candidate genes on 5q31-33 resequenced for an asthma candidate gene based study was also used for the analysis. RESULTS: A total of 237 SNPs were identified through resequencing of which only 95 SNPs (40%) were in Hapmap; however an additional 56 SNPs (24%) were not genotyped directly but had a proxy SNP in the Hapmap. At the genome-wide level, Singapore Chinese were highly correlated with Hapmap Han Chinese with correlation of 0.954 and 0.947 for the Illumina and Affymetrix platforms respectively with deviant SNPs randomly distributed within and across all chromosomes. CONCLUSIONS: The high correlation between our population and Hapmap Han Chinese reaffirms the applicability of Hapmap based genome-wide chips for GWA studies. There is a clear population signature for the Singapore Chinese samples and they predominantly resemble the southern Han Chinese population; however when new migrants particularly those with northern Han Chinese background were included, population stratification issues may arise. Future studies needs to address population stratification within the sample collection while designing and interpreting GWAS in the Chinese population.
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spelling pubmed-28776512010-05-27 Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population Andiappan, Anand Kumar Anantharaman, Ramani Nilkanth, Pallavi Parate Wang, De Yun Chew, Fook Tim BMC Genet Research article BACKGROUND: The International Hapmap project serves as a valuable resource for human genome variation data, however its applicability to other populations has yet to be exhaustively investigated. In this paper, we use high density genotyping chips and resequencing strategies to compare the Singapore Chinese population with the Hapmap populations. First we compared 1028 and 114 unrelated Singapore Chinese samples genotyped using the Illumina Human Hapmap 550 k chip and Affymetrix 500 k array respectively against the 270 samples from Hapmap. Secondly, data from 20 candidate genes on 5q31-33 resequenced for an asthma candidate gene based study was also used for the analysis. RESULTS: A total of 237 SNPs were identified through resequencing of which only 95 SNPs (40%) were in Hapmap; however an additional 56 SNPs (24%) were not genotyped directly but had a proxy SNP in the Hapmap. At the genome-wide level, Singapore Chinese were highly correlated with Hapmap Han Chinese with correlation of 0.954 and 0.947 for the Illumina and Affymetrix platforms respectively with deviant SNPs randomly distributed within and across all chromosomes. CONCLUSIONS: The high correlation between our population and Hapmap Han Chinese reaffirms the applicability of Hapmap based genome-wide chips for GWA studies. There is a clear population signature for the Singapore Chinese samples and they predominantly resemble the southern Han Chinese population; however when new migrants particularly those with northern Han Chinese background were included, population stratification issues may arise. Future studies needs to address population stratification within the sample collection while designing and interpreting GWAS in the Chinese population. BioMed Central 2010-05-07 /pmc/articles/PMC2877651/ /pubmed/20459637 http://dx.doi.org/10.1186/1471-2156-11-36 Text en Copyright ©2010 Andiappan 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
Andiappan, Anand Kumar
Anantharaman, Ramani
Nilkanth, Pallavi Parate
Wang, De Yun
Chew, Fook Tim
Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
title Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
title_full Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
title_fullStr Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
title_full_unstemmed Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
title_short Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population
title_sort evaluating the transferability of hapmap snps to a singapore chinese population
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877651/
https://www.ncbi.nlm.nih.gov/pubmed/20459637
http://dx.doi.org/10.1186/1471-2156-11-36
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