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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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| Publicado no: | Genet Sel Evol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5320806/ https://ncbi.nlm.nih.gov/pubmed/28222685 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12711-017-0301-x |
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