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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Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Applications Note
Acesso em linha: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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