Accurate sequence variant genotyping in cattle using variation-aware genome graphs

BACKGROUND: Genotyping of sequence variants typically involves, as a first step, the alignment of sequencing reads to a linear reference genome. Because a linear reference genome represents only a small fraction of all the DNA sequence variation within a species, reference allele bias may occur at h...

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Detalles Bibliográficos
Autores principales: Crysnanto, Danang, Wurmser, Christine, Pausch, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521551/
https://www.ncbi.nlm.nih.gov/pubmed/31092189
http://dx.doi.org/10.1186/s12711-019-0462-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521551/
https://www.ncbi.nlm.nih.gov/pubmed/31092189
http://dx.doi.org/10.1186/s12711-019-0462-x

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