Evaluation of the accuracy of imputed sequence variant genotypes and their utility for causal variant detection in cattle

BACKGROUND: The availability of dense genotypes and whole-genome sequence variants from various sources offers the opportunity to compile large datasets consisting of tens of thousands of individuals with genotypes at millions of polymorphic sites that may enhance the power of genomic analyses. The...

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Detalles Bibliográficos
Autores principales: Pausch, Hubert, MacLeod, Iona M., Fries, Ruedi, Emmerling, Reiner, Bowman, Phil J., Daetwyler, Hans D., Goddard, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320806/
https://www.ncbi.nlm.nih.gov/pubmed/28222685
http://dx.doi.org/10.1186/s12711-017-0301-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320806/
https://www.ncbi.nlm.nih.gov/pubmed/28222685
http://dx.doi.org/10.1186/s12711-017-0301-x

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