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Genomic Prediction Based on SNP Functional Annotation Using Imputed Whole-Genome Sequence Data in Korean Hanwoo
Bryan Irvine M Lopez1, Narae An1, Krishnamoorthy Srikanth1
1Division of Animal Genomics and Bioinformatics, National Institute of Animal Science, Rural Development Administration, Wanju, South Korea.
Adding selected variants from whole-genome sequence (WGS) data significantly improves genomic predictions for Hanwoo cattle carcass traits. Incorporating 3000 variants per trait enhanced prediction accuracy, demonstrating WGS data
Area of Science:
- Animal Genomics
- Quantitative Genetics
- Livestock Breeding
Background:
- Whole-genome sequence (WGS) data offers higher predictive ability in genomic predictions by including causal mutations.
- Existing SNP panels may not capture all relevant genetic variation for complex traits.
- Improving genomic prediction accuracy is crucial for efficient livestock breeding programs.
Purpose of the Study:
- To enhance the predictive performance of the Hanwoo 50k SNP panel for four carcass traits.
- To investigate the utility of adding pre-selected variants from WGS data to a customized SNP panel.
- To evaluate the impact of different functional annotations on predictive power.
Main Methods:
- Utilized WGS imputed genotypes and phenotypes from 16,892 Hanwoo cattle for four carcass traits.
- Performed genome-wide association studies (GWAS) for variant pre-selection.
- Added sets of pre-selected SNPs (1000-10,000) to the 50k panel and assessed predictive performance using GBLUP.
Main Results:
- Adding 3000 pre-selected variants per trait to the 50k panel improved prediction accuracies by up to 9.9%.
- The inclusion of 12,000 variants (3000 per trait) increased prediction accuracies for backfat thickness, carcass weight, longissimus muscle area, and marbling score.
- Pre-selected SNPs from the intergenic region (IGR) showed the highest improvement, comparable to using whole-genome data.
Conclusions:
- The predictive performance of the Hanwoo 50k SNP panel can be effectively improved by incorporating selected variants from WGS data.
- The optimal number of added variants appears to be trait-dependent, with 3000 per trait being sufficient for significant improvement.
- While IGR variants showed promise, WGS data generally provided higher accuracy than specific genomic regions.
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