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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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| Main Authors: | , , , , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2011
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| Teme: | |
| Online dostop: | 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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