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...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Asian-Australasian journal of animal sciences. - 1998. - 27(2014), 12 vom: 31. Dez., Seite 1691-4
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| 1. Verfasser: |
Kim, HyoYoung
(VerfasserIn) |
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| Weitere Verfasser: |
Sung, Samsun,
Cho, Seoae,
Kim, Tae-Hun,
Seo, Kangseok,
Kim, Heebal |
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| Format: | Online-Aufsatz
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| Sprache: | English |
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| Veröffentlicht: |
2014
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| Zugriff auf das übergeordnete Werk: | Asian-Australasian journal of animal sciences
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| Schlagworte: | Journal Article
Copy Number Variation
Cytomap
Homozygosity
Single Nucleotide Polymorphism
Visualization |
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