Pregled bibliografske jedinice broj: 697205
Genome-wide meta-analysis of autosomal SNP differences between men and women
Genome-wide meta-analysis of autosomal SNP differences between men and women // Poster Abstracts: 12th International Congress of Human Genetics/61st Annual Meeting of The American Society of Human Genetics
Montréal, Kanada, 2011. str. 399F-399F (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 697205 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genome-wide meta-analysis of autosomal SNP differences between men and women
Autori
Boraska, Vesna ; Jeroncic, Ana ; Colonna, Vincenza i sur.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Poster Abstracts: 12th International Congress of Human Genetics/61st Annual Meeting of The American Society of Human Genetics
/ - , 2011, 399F-399F
Skup
12th International Congress of Human Genetics/61st Annual Meeting of The American Society of Human Genetics
Mjesto i datum
Montréal, Kanada, 11.10.2011. - 15.10.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
genome-wide; meta-analysis; autosomal SNP; gender differences
Sažetak
Introduction: The male-to-female sex ratio at birth is constant across world populations, ranging between 1.02-1.08 (102-108 male to 100 female live births), with an average of 1.06 for populations of European descent. Sex ratio is considered to be affected by numerous biological and environmental factors, and has been suggested to have a heritable component. The aim of the present study is to investigate the presence of common-allele modest effects at autosomal variants that could explain the observed sex ratio at birth. We also conducted a simulation study to assess the probability of observing significant allele frequency differences at autosomal markers between men and women. Methods: We conducted fixed and random-effects large-scale genome-wide scan (GWAS) meta-analysis across 51 studies, comprising overall 114, 863 individuals (61, 094 women and 53, 769 men) of European ancestry. Allele frequencies were compared between men and women for directly-typed and imputed common (minor allele frequency >0.05) variants within each study. Forward-time simulations for unlinked neutral biallelic loci were performed under the demographic model for European populations. Results and Discussion: We did not detect any genome-wide significant (p<5x10-8) autosomal common SNP differences between men and women in the meta-analysis. We also observed no frequency differences between men and women in our simulation of 1.3 million common loci in a cohort matching the study sample. Conclusion: This large-scale investigation across ~115, 000 individuals shows no detectable contribution from common genetic variants to the observed skew in sex ratio. The absence of sex- specific differences is useful in guiding genetic association study design, for example when using mixed controls for sex-biased traits.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Split