Using pre-selected variants from large-scale whole-genome sequence data for single-step genomic predictions in pigs

BACKGROUND: Whole-genome sequence (WGS) data harbor causative variants that may not be present in standard single nucleotide polymorphism (SNP) chip data. The objective of this study was to investigate the impact of using preselected variants from WGS for single-step genomic predictions in maternal...

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Detalles Bibliográficos
Autores principales: Jang, Sungbong, Ros-Freixedes, Roger, Hickey, John M., Chen, Ching-Yi, Holl, Justin, Herring, William O., Misztal, Ignacy, Lourenco, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373252/
https://www.ncbi.nlm.nih.gov/pubmed/37495982
http://dx.doi.org/10.1186/s12711-023-00831-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373252/
https://www.ncbi.nlm.nih.gov/pubmed/37495982
http://dx.doi.org/10.1186/s12711-023-00831-0

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