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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Applications Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129530/
https://www.ncbi.nlm.nih.gov/pubmed/21624899
http://dx.doi.org/10.1093/bioinformatics/btr317

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129530/
https://www.ncbi.nlm.nih.gov/pubmed/21624899
http://dx.doi.org/10.1093/bioinformatics/btr317

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