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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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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST)
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4213679/ https://ncbi.nlm.nih.gov/pubmed/25358361 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5713/ajas.2014.14143 |
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