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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...
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| Publicado no: | Genet Sel Evol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6521551/ https://ncbi.nlm.nih.gov/pubmed/31092189 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12711-019-0462-x |
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