Abstract

A beef cattle population (n=2,343) was used to assess the impact of variants identified from imputed lowpass sequence on the genetic prediction of birth weight (BWT) and post weaning gain (PWG). Variants (n=1,145,892) were selected based on functional impact and were partitioned into low, modifier, moderate, and high based on predicted functional consequences. Each subset was used to construct a genomic relationship matrix (GRM) in univariate animal models. When all variants were included in a single GRM, heritability estimates for BWT and PWG were 0.41±0.05 and 0.37±0.05, respectively. Heritability estimates for BWT when the GRM was comprised of only low, modifier, moderate, or high variants were 0.36±0.05, 0.39±0.05, 0.33±0.05, and 0.10±0.03, respectively. Similar estimates for PWG were 0.33±0.05, 0.34±0.05, 0.32±0.05, and 0.10±0.03, respectively. Results suggest that despite predicted functional consequences, the high variants accounted for only ~24-27% of the genetic variance. The USDA is an equal opportunity employer and provider.

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