Trios-Based Inquiry into de novo CNVs in Swine Genome

This project aimed to quantify the prevalence of de novo copy number variations (CNVs) within the porcine genome using whole-genome sequencing data. In addition to estimating de novo mutation rates, we characterized the genomic distribution of these polymorphisms. Furthermore, we conducted comparative analyses between de novo and inherited CNVs, focusing on their length and frequency, while also assessing their functional implications within the genome.