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Prioritizing single-nucleotide polymorphisms and variants associated with clinical mastitis
Next-generation sequencing technology has provided resources to easily explore and identify candidate single-nucleotide polymorphisms (SNPs) and variants. However, there remains a challenge in identifying and inferring the causal SNPs from sequence data. A problem with different methods that predict...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473491/ https://www.ncbi.nlm.nih.gov/pubmed/28652783 http://dx.doi.org/10.2147/AABC.S123604 |