VING: a software for visualization of deep sequencing signals.
BMC Res Notes
; 8: 419, 2015 Sep 07.
Article
em En
| MEDLINE
| ID: mdl-26346985
ABSTRACT
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 NGS data coverage, especially when multiple experiments are simultaneously treated.RESULTS:
We developed 'VING', a stand-alone R script that takes as input NGS mapping files and genome annotations to produce accurate snapshots of the NGS coverage signal for any specified genomic region. VING offers multiple viewing options, including strand-specific views and a special heatmap mode for representing multiple experiments in a single figure.CONCLUSIONS:
VING produces high-quality figures for NGS data representation in a genome region of interest. It is available at http//vm-gb.curie.fr/ving/. We also developed a Galaxy wrapper, available in the Galaxy tool shed with installation and usage instructions.
Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Software
/
Genoma
/
Análise de Sequência de DNA
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Sequenciamento de Nucleotídeos em Larga Escala
Idioma:
En
Revista:
BMC Res Notes
Ano de publicação:
2015
Tipo de documento:
Article
País de afiliação:
França