Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) that contribute to phenotypic diversity. Compared to SNP, a CNV can cover a wider chromosome region,
Additional file 2: Genome-wide significant SNPs per trait: Results of GWAS summary statistics for all genome-wide significant SNPs identified per analysed trait. Results are separate for each trait, n
ABSTRACT The present investigation aimed to evaluate the population structure and inbreeding of Holstein herds in southern Brazil. To carry out the analysis, the Associação Paranaense de Criadores de
