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High-resolution structural variants catalogue in a large-scale whole genome sequenced bovine family cohort data
BACKGROUND: Structural variants (SVs) are chromosomal segments that differ between genomes, such as deletions, duplications, insertions, inversions and translocations. The genomics revolution enabled the discovery of sub-microscopic SVs via array and whole-genome sequencing (WGS) data, paving the wa...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152703/ https://www.ncbi.nlm.nih.gov/pubmed/37127590 http://dx.doi.org/10.1186/s12864-023-09259-8 |