Highly accurate sequence imputation enables precise QTL mapping in Brown Swiss cattle
Abstract
BACKGROUND:
Within the last few years a large amount of genomic information has become available in cattle. Densities of genomic information vary from a few thousand variants up to whole genome sequence information. In order to combine genomic information from different sources and infer genotypes for a common set of variants, genotype imputation is required.
RESULTS:
In this study we evaluated the accuracy of imputation from high density chips to whole genome sequence data in Brown Swiss cattle. Using four popular imputation programs (Beagle, FImpute, Impute2, Minimac) and various compositions of reference panels, the accuracy of the imputed sequence variant genotypes was high and differences between the programs and scenarios were small. We imputed sequence variant genotypes for more than 1600 Brown Swiss bulls and performed genome-wide association studies for milk fat percentage at two stages of lactation. We found one and three quantitative trait loci for early and late lactation fat content, respectively. Known causal variants that were imputed from the sequenced reference panel were among the most significantly associated variants of the genome-wide association study.
CONCLUSIONS:
Our study demonstrates that whole-genome sequence information can be imputed at high accuracy in cattle populations. Using imputed sequence variant genotypes in genome-wide association studies may facilitate causal variant detection. Show more
Permanent link
https://doi.org/10.3929/ethz-b-000225342Publication status
publishedExternal links
Journal / series
BMC GenomicsVolume
Pages / Article No.
Publisher
BioMed CentralSubject
Whole genome sequencing; Imputation; Accuracy; Genome-wide association study; QTL discovery; Milk traits; Brown Swiss; Dairy cattleOrganisational unit
09575 - Pausch, Hubert / Pausch, Hubert
More
Show all metadata