bioRxiv (Cold Spring Harbor Laboratory) · 2021 · 15 citations · 61 references
Life SciencesGeneticsMolecular GeneticsGenomic Data AnalysisGenomicsTranscriptomicsAnimal GenomicsPan-genome AnalysisStructural Variant AnalysisVariant AnalysisVariant CallingVariant DetectionAnimal Pan-genomicsBenchmarking Genome AssembliesInsertionsPan-genome AssemblyPan-genome GraphsRna Sequencing Data IntegrationRna-seq AssemblyStructural Variant Integration
Abstract Structural variations (SVs) are a major contributor to genetic diversity and phenotypic variations, but their prevalence and functions in domestic animals are largely unexplored. Here, we assembled 26 haplotype-resolved genome assemblies from 13 genetically diverse sheep using PacBio HiFi sequencing. We constructed a graph-based ovine pan-genome and discovered 142,422 biallelic insertions and deletions, 7,028 divergent alleles and 13,419 multiallelic variations. We then used a graph-based approach to genotype the biallelic SVs in 684 individuals from 45 domestic breeds and two wild species. Integration with RNA-seq data allows to identify candidate expression-associated SVs. We demonstrate a direct link of SVs and phenotypes by localizing the putative causative insertion in HOXB13 gene responsible for the long-tail trait and identifying multiple large SVs associated with the fat-tail. Beyond generating a benchmark resource for ovine structural variants, our study highlights that animal genetic research will greatly benefit from using a pan-genome graph rather than a single reference genome.
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