“…The high and low LD discovered throughout the three genomes provide a high possibility of locating target QTL with large and minor impacts in the existing materials [68] . High LDs were identified between significant markers on the same chromosome, indicating that these markers are frequently co-inherited [69] . One marker from each high LD genomic region can be selected and transformed into a kompetitive allele-specific PCR (KASP) marker for further validation in a different genetic context [70] , [71] .…”