Using population-specific add-on polymorphisms to improve genotype imputation in underrepresented populations
Xu ZMPapers in this archive, Rüeger SPapers in this archive, Zwyer MPapers in this archive, Brites DPapers in this archive, Hiza HPapers in this archive, Reinhard MPapers in this archive, Rutaihwa LPapers in this archive, Borrell SPapers in this archive, Isihaka FPapers in this archive, Temba HPapers in this archive, Maroa TPapers in this archive, Naftari RPapers in this archive, Hella JPapers in this archive, Sasamalo MPapers in this archive, Reither KPapers in this archive, Portevin DPapers in this archive, Gagneux SPapers in this archive, Fellay JPapers in this archive
Abstract
Genome-wide association studies rely on the statistical inference of untyped variants, called imputation, to increase the coverage of genotyping arrays. However, the results are often suboptimal in populations underrepresented in existing reference panels and array designs, since the selected single nucleotide polymorphisms (SNPs) may fail to capture population-specific haplotype structures, hence the full extent of common genetic variation. Here, we propose to sequence the full genomes of a small subset of an underrepresented study cohort to inform the selection of population-specific add-on tag SNPs and to generate an internal population-specific imputation reference panel, such that the remaining array-genotyped cohort could be more accurately imputed. Using a Tanzania-based cohort as a proof-of-concept, we demonstrate the validity of our approach by showing improvements in imputation accuracy after the addition of our designed add-on tags to the base H3Africa array.
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