A comparison of genotyping-by-sequencing analysis methods on low-coverage crop datasets shows advantages of a new workflow, GB-eaSy

BACKGROUND: Genotyping-by-sequencing (GBS), a method to identify genetic variants and quickly genotype samples, reduces genome complexity by using restriction enzymes to divide the genome into fragments whose ends are sequenced on short-read sequencing platforms. While cost-effective, this method pr...

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Detalles Bibliográficos
Autores principales: Wickland, Daniel P., Battu, Gopal, Hudson, Karen A., Diers, Brian W., Hudson, Matthew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745977/
https://www.ncbi.nlm.nih.gov/pubmed/29281959
http://dx.doi.org/10.1186/s12859-017-2000-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745977/
https://www.ncbi.nlm.nih.gov/pubmed/29281959
http://dx.doi.org/10.1186/s12859-017-2000-6

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