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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Bibliografiska uppgifter
Huvudupphovsmän: Preston, Mark D., Manske, Magnus, Horner, Neil, Assefa, Samuel, Campino, Susana, Auburn, Sarah, Zongo, Issaka, Ouedraogo, Jean-Bosco, Nosten, Francois, Anderson, Tim, Clark, Taane G.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2012
Ämnen:
Applications Note
Länkar: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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