“…Thus, clonal field trials with family structure are a more common method to estimate non-additive, in particular, epistatic genetic variance. Currently, genomic data with numerous markers distributed genome-wide using exome capture (Thistlethwaite et al 2017;Chen et al 2019), Genotypingby-sequencing (GBS) (Ratcliffe et al 2015) or SNP-chips (Tan et al 2018) are becoming gradually available and genomic relationship matrices for additive, dominance, and epistatic effects can be calculated to estimate the additive, dominance, and epistasis genetic variances. Predicted genomic breeding values can also be compared with the traditional pedigree-based breeding values (Muñoz et al 2014).…”