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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2019
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| 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 |