Abstract #65
Section: Breeding and Genetics (orals)
Session: Joint ADSA/Interbull Session: Breeding and Genetics: Ten Years of Genomic Selection
Format: Oral
Day/Time: Monday 9:30 AM–10:00 AM
Location: Junior Ballroom C
Session: Joint ADSA/Interbull Session: Breeding and Genetics: Ten Years of Genomic Selection
Format: Oral
Day/Time: Monday 9:30 AM–10:00 AM
Location: Junior Ballroom C
# 65
From sequence of Dominette to 10K and 50K SNP chips.
D. Bickhart*1, 1USDA Agricultural Research Service Dairy Forage Research Center, Madison, WI.
Key Words: SNP chip, cattle reference, genomics
From sequence of Dominette to 10K and 50K SNP chips.
D. Bickhart*1, 1USDA Agricultural Research Service Dairy Forage Research Center, Madison, WI.
Genetic markers based on interrogated nucleotide variant sites have been used in cattle genetics since the late 1990s. Owing partly to the excessive cost and labor-intensive means of assessing marker sites, such as microsatellite repeats, their commercial use was relatively limited. Additionally, genotyping accuracy was error-prone and did not cover the cattle genome evenly. In this presentation, we highlight 2 specific improvements that started the modern genomics era. The development of high-resolution DNA sequence maps of the cattle genome and the adaptation of microarrays for high throughput genotyping served as the catalysts for data collection for modern cattle genomic selection. Simultaneously, the development of computational methods for associating animal SNP genotypes with productive trait phenotypes improved the accuracy of animal selective breeding values by providing higher resolution of allelic transmission to offspring. The efficacy of these tandem improvements has generated incredible value for the modern cattle breeder; however, many challenges and questions persist. Linkage between genetic markers and their associated causal genetic mutations can be further improved by genotyping the actual mutation itself. There is additional novel sequence within the cattle pan-genome that is currently not represented in the cattle reference genome assembly, which may not be tracked by current genetic markers. Finally, methods need to be developed that efficiently incorporate whole genome DNA sequence data into genomic selection. Future techniques and technologies that may address these challenges will be discussed.
Key Words: SNP chip, cattle reference, genomics