VCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism

Copy number variation (CNV) or single nucleotide phlyorphism (SNP) is useful genetic resource to aid in understanding complex phenotypes or deseases susceptibility. Although thousands of CNVs and SNPs are currently avaliable in the public databases, they are somewhat difficult to use for analyses wi...

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Detalles Bibliográficos
Autores principales: Kim, HyoYoung, Sung, Samsun, Cho, Seoae, Kim, Tae-Hun, Seo, Kangseok, Kim, Heebal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213679/
https://www.ncbi.nlm.nih.gov/pubmed/25358361
http://dx.doi.org/10.5713/ajas.2014.14143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213679/
https://www.ncbi.nlm.nih.gov/pubmed/25358361
http://dx.doi.org/10.5713/ajas.2014.14143

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