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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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| Gepubliceerd in: | BMC Res Notes |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2015
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| Onderwerpen: | |
| Online toegang: | 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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