SVA: software for annotating and visualizing sequenced human genomes

Summary: Here we present Sequence Variant Analyzer (SVA), a software tool that assigns a predicted biological function to variants identified in next-generation sequencing studies and provides a browser to visualize the variants in their genomic contexts. SVA also provides for flexible interaction w...

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Detaylı Bibliyografya
Asıl Yazarlar: Ge, Dongliang, Ruzzo, Elizabeth K., Shianna, Kevin V., He, Min, Pelak, Kimberly, Heinzen, Erin L., Need, Anna C., Cirulli, Elizabeth T., Maia, Jessica M., Dickson, Samuel P., Zhu, Mingfu, Singh, Abanish, Allen, Andrew S., Goldstein, David B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2011
Konular:
Applications Note
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3129530/
https://ncbi.nlm.nih.gov/pubmed/21624899
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr317
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