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...

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Detalles Bibliográficos
Autores principales: Suravajhala, Prashanth, Benso, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Hypothesis
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

Internet

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

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