Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations.
Reisberg, Sulev; Galwey, Nicholas; Avillach, Paul; Sahlqvist, Anna-Stina; Kolberg, Liis; Mägi, Reedik; Esko, Tõnu; Vilo, Jaak; James, Glen.
Int J Immunogenet
; 46(2): 49-58, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30659741
Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.
A 1000 Arab genome project to study the Emirati population.
Robust prediction of expression differences among human individuals using only genotype information.
Inference of historical migration rates via haplotype sharing.
Estimating and interpreting FST: the impact of rare variants.
Addressing population-specific multiple testing burdens in genetic association studies.
Empirical testing of a 23-AIMs panel of SNPs for ancestry evaluations in four major US populations.
Power comparison of admixture mapping and direct association analysis in genome-wide association studies.
Identifying recent adaptations in large-scale genomic data.
Selection of highly informative SNP markers for population affiliation of major US populations.