Fig. 10From: Efficient genomic prediction based on whole-genome sequence data using split-and-merge Bayesian variable selectionBayes factors greater than 1 for SCS using 50k SNPs and increasingly more selected sequence-based variants. Considered sets of variants are the 50k SNPs, or the 50k SNPs plus increasingly larger subsets (1060 to 460,158) of variantsBack to article page