Location: Cell Wall Biology and Utilization Research
Title: Genome-wide copy number variation and structural variation: A novel tool for improved livestock genomic selectionAuthor
Submitted to: Book Chapter
Publication Type: Book / Chapter Publication Acceptance Date: 9/23/2023 Publication Date: N/A Citation: N/A Interpretive Summary: Technical Abstract: Copy number variations (CNVs) are a major form of genomic variation in mammalian genomes. Due to their much larger size than single nucleotide polymorphisms (SNPs), they affect a significant portion of the genome via deletion, duplication, and translocation. SNPs have been the variant of choice in genomic prediction in livestock species. With the advancement of sequencing technologies and analytical algorithms, a significant number of CNVs have been associated with desirable production traits and disease phenotypes, making this form of genomic variant an attractive candidate for improved livestock genomic selection. In this review, the current CNVs associated with livestock production traits and diseases, and the obstacles of using CNVs for genomic selection are discussed. Finally, this review discusses how CNVs can be used in the future to improve livestock genomic selection. |