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VarB: a variation browsing and analysis tool for variants derived from next-generation sequencing data
Summary: There is an immediate need for tools to both analyse and visualize in real-time single-nucleotide polymorphisms, insertions and deletions, and other structural variants from new sequence file formats. We have developed VarB software that can be used to visualize variant call format files in...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3496337/ https://ncbi.nlm.nih.gov/pubmed/22976080 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts557 |
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