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Assessing the impact of global versus local ancestry in association studies
BACKGROUND: To account for population stratification in association studies, principal-components analysis is often performed on single-nucleotide polymorphisms (SNPs) across the genome. Here, we use Framingham Heart Study (FHS) Genetic Analysis Workshop 16 data to compare the performance of local a...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795878/ https://www.ncbi.nlm.nih.gov/pubmed/20017971 |
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author | Kang, Sun Jung Larkin, Emma K Song, Yeunjoo Barnholtz-Sloan, Jill Baechle, Dan Feng, Tao Zhu, Xiaofeng |
author_facet | Kang, Sun Jung Larkin, Emma K Song, Yeunjoo Barnholtz-Sloan, Jill Baechle, Dan Feng, Tao Zhu, Xiaofeng |
author_sort | Kang, Sun Jung |
collection | PubMed |
description | BACKGROUND: To account for population stratification in association studies, principal-components analysis is often performed on single-nucleotide polymorphisms (SNPs) across the genome. Here, we use Framingham Heart Study (FHS) Genetic Analysis Workshop 16 data to compare the performance of local ancestry adjustment for population stratification based on principal components (PCs) estimated from SNPs in a local chromosomal region with global ancestry adjustment based on PCs estimated from genome-wide SNPs. METHODS: Standardized height residuals from unrelated adults from the FHS Offspring Cohort were averaged from longitudinal data. PCs of SNP genotype data were calculated to represent individual's ancestry either 1) globally using all SNPs across the genome or 2) locally using SNPs in adjacent 20-Mbp regions within each chromosome. We assessed the extent to which there were differences in association studies of height depending on whether PCs for global, local, or both global and local ancestry were included as covariates. RESULTS: The correlations between local and global PCs were low (r < 0.12), suggesting variability between local and global ancestry estimates. Genome-wide association tests without any ancestry adjustment demonstrated an inflated type I error rate that decreased with adjustment for local ancestry, global ancestry, or both. A known spurious association was replicated for SNPs within the lactase gene, and this false-positive association was abolished by adjustment with local or global ancestry PCs. CONCLUSION: Population stratification is a potential source of bias in this seemingly homogenous FHS population. However, local and global PCs derived from SNPs appear to provide adequate information about ancestry. |
format | Text |
id | pubmed-2795878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27958782009-12-18 Assessing the impact of global versus local ancestry in association studies Kang, Sun Jung Larkin, Emma K Song, Yeunjoo Barnholtz-Sloan, Jill Baechle, Dan Feng, Tao Zhu, Xiaofeng BMC Proc Proceedings BACKGROUND: To account for population stratification in association studies, principal-components analysis is often performed on single-nucleotide polymorphisms (SNPs) across the genome. Here, we use Framingham Heart Study (FHS) Genetic Analysis Workshop 16 data to compare the performance of local ancestry adjustment for population stratification based on principal components (PCs) estimated from SNPs in a local chromosomal region with global ancestry adjustment based on PCs estimated from genome-wide SNPs. METHODS: Standardized height residuals from unrelated adults from the FHS Offspring Cohort were averaged from longitudinal data. PCs of SNP genotype data were calculated to represent individual's ancestry either 1) globally using all SNPs across the genome or 2) locally using SNPs in adjacent 20-Mbp regions within each chromosome. We assessed the extent to which there were differences in association studies of height depending on whether PCs for global, local, or both global and local ancestry were included as covariates. RESULTS: The correlations between local and global PCs were low (r < 0.12), suggesting variability between local and global ancestry estimates. Genome-wide association tests without any ancestry adjustment demonstrated an inflated type I error rate that decreased with adjustment for local ancestry, global ancestry, or both. A known spurious association was replicated for SNPs within the lactase gene, and this false-positive association was abolished by adjustment with local or global ancestry PCs. CONCLUSION: Population stratification is a potential source of bias in this seemingly homogenous FHS population. However, local and global PCs derived from SNPs appear to provide adequate information about ancestry. BioMed Central 2009-12-15 /pmc/articles/PMC2795878/ /pubmed/20017971 Text en Copyright ©2009 Kang 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 | Proceedings Kang, Sun Jung Larkin, Emma K Song, Yeunjoo Barnholtz-Sloan, Jill Baechle, Dan Feng, Tao Zhu, Xiaofeng Assessing the impact of global versus local ancestry in association studies |
title | Assessing the impact of global versus local ancestry in association studies |
title_full | Assessing the impact of global versus local ancestry in association studies |
title_fullStr | Assessing the impact of global versus local ancestry in association studies |
title_full_unstemmed | Assessing the impact of global versus local ancestry in association studies |
title_short | Assessing the impact of global versus local ancestry in association studies |
title_sort | assessing the impact of global versus local ancestry in association studies |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795878/ https://www.ncbi.nlm.nih.gov/pubmed/20017971 |
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