“…Over a decade of improvements in sequencing technology, whole-genome sequencing and modified reduced genome sequencing (e.g., RAD, RRGS, and GBS) have occurred and SNPs are the most common markers in recent studies [89][90][91]. Currently, multiple genomic variant types, including copy number variations (CNVs) [92][93][94], insertion-deletion (InDel) [84,95], structure variations (SV) [96][97][98], haplotype [99], presence/absence variations (PAVs) based on pan-genome [100], and even epigenomic markers [101] have gained increasing attention through GWAS. Multiple variant profiles have been generated for multiple breeds [102,103].…”