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Trans-ethnic study design approaches for fine-mapping
- Source :
- European Journal of Human Genetics
- Publication Year :
- 2016
- Publisher :
- Springer Science and Business Media LLC, 2016.
-
Abstract
- Studies that traverse ancestrally diverse populations may increase power to detect novel loci and improve fine-mapping resolution of causal variants by leveraging linkage disequilibrium differences between ethnic groups. The inclusion of African ancestry samples may yield further improvements because of low linkage disequilibrium and high genetic heterogeneity. We investigate the fine-mapping resolution of trans-ethnic fixed-effects meta-analysis for five type II diabetes loci, under various settings of ancestral composition (European, East Asian, African), allelic heterogeneity, and causal variant minor allele frequency. In particular, three settings of ancestral composition were compared: (1) single ancestry (European), (2) moderate ancestral diversity (European and East Asian), and (3) high ancestral diversity (European, East Asian, and African). Our simulations suggest that the European/Asian and European ancestry-only meta-analyses consistently attain similar fine-mapping resolution. The inclusion of African ancestry samples in the meta-analysis leads to a marked improvement in fine-mapping resolution.
- Subjects :
- 0301 basic medicine
Linkage disequilibrium
media_common.quotation_subject
Ethnic group
030105 genetics & heredity
Biology
Polymorphism, Single Nucleotide
Article
Linkage Disequilibrium
Genetic Heterogeneity
03 medical and health sciences
Meta-Analysis as Topic
Genetic linkage
Genetics
Humans
East Asia
Genetics (clinical)
media_common
Models, Genetic
Genetic heterogeneity
Racial Groups
Chromosome Mapping
Pedigree
Minor allele frequency
030104 developmental biology
Diabetes Mellitus, Type 2
Genetic Loci
Research Design
Allelic heterogeneity
Algorithms
Genome-Wide Association Study
Diversity (politics)
Subjects
Details
- ISSN :
- 14765438 and 10184813
- Volume :
- 24
- Database :
- OpenAIRE
- Journal :
- European Journal of Human Genetics
- Accession number :
- edsair.doi.dedup.....eb73c309ab02a111bfb359c8d7e53eac
- Full Text :
- https://doi.org/10.1038/ejhg.2016.1