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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Bibliographic Details
Published in:Genet Sel Evol
Main Authors: Pausch, Hubert, MacLeod, Iona M., Fries, Ruedi, Emmerling, Reiner, Bowman, Phil J., Daetwyler, Hans D., Goddard, Michael E.
Format: Artigo
Language:Inglês
Published: BioMed Central 2017
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Research Article
Online Access: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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