European American Stratification in Ovarian Cancer Case Control Data: The Utility of Genome-Wide Data for Inferring Ancestry
Year: 2012
Type: article
Abstract: We investigated the ability of several principal components analysis (PCA)-based strategies to detect and control for population stratification using data from a multi-center study of epithelial ovarian cancer among women of European-American ethnicity. These include a correction based on an ancestry informative markers (AIMs) panel designed to capture European ancestral variation and corrections utilizing un-thinned genome-wide SNP data; case-control samples were drawn from four geographically distinct North-American sites. The AIMs-only and genome-wide first principal components (PC1) both corresponded to the previously described North or Northwest-Southeast axis of European variation. We found that the genome-wide PCA captured this primary dimension of variation more precisely and identified additional axes of genome-wide variation of relevance to epithelial ovarian cancer. Associations evident between the genome-wide PCs and study site corroborate North American immigration history and suggest that undiscovered dimensions of variation lie within Northern Europe. The structure captured by the genome-wide PCA was also found within control individuals and did not reflect the case-control variation present in the data. The genome-wide PCA highlighted three regions of local LD, corresponding to the lactase (LCT) gene on chromosome 2, the human leukocyte antigen system (HLA) on chromosome 6 and to a common inversion polymorphism on chromosome 8. These features did not compromise the efficacy of PCs from this analysis for ancestry control. This study concludes that although AIMs panels are a cost-effective way of capturing population structure, genome-wide data should preferably be used when available.
Source: PLoS ONE
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,382
Awards: G1325448431, Population-Based Analysis of Ovarian Cancer Biomarkers, The Molecular Epidemiology Of Ovarian Cancer, G317494032, G3706033545, G401803774, GENETIC/EPIDEMIOLOGY STUDY OF EPITHELIAL OVARIAN TUMORS, Genetic Variation in the NF-kappaB Pathway and Ovarian Cancer Etiology, RISK FACTOR ANALYSIS OF BRCA1 AND BRCA2 CARRIERS, G844520391, Haplotype-Based Genome Screen for Ovarian Cancer Loci, G883206123, G9000126810, Mayo Clinic Comprehensive Cancer Center Support Grant, Moffitt Cancer Center Support Grant, Mayo Clinic Ovarian Cancer SPORE, G917257176
OpenAlex ID: W1997070555
