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

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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Bibliographic Details
Main Authors:	HyoYoung Kim, Samsun Sung, Seoae Cho, Tae-Hun Kim, Kangseok Seo, Heebal Kim
Format:	Article
Language:	English
Published:	Asian-Australasian Association of Animal Production Societies 2014-12-01
Series:	Asian-Australasian Journal of Animal Sciences
Subjects:	Copy Number Variation Cytomap Homozygosity Single Nucleotide Polymorphism Visualization
Online Access:	http://www.ajas.info/upload/pdf/ajas-27-12-1691.pdf

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