VING: a software for visualization of deep sequencing signals

BACKGROUND: Next generation sequencing (NGS) data treatment often requires mapping sequenced reads onto a reference genome for further analysis. Mapped data are commonly visualized using genome browsers. However, such software are not suited for a publication-ready and versatile representation of NG...

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Enregistré dans:
Détails bibliographiques
Publié dans:BMC Res Notes
Auteurs principaux: Descrimes, Marc, Zouari, Yousra Ben, Wery, Maxime, Legendre, Rachel, Gautheret, Daniel, Morillon, Antonin
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2015
Sujets:
Technical Note
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4562374/
https://ncbi.nlm.nih.gov/pubmed/26346985
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1404-5
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