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Content provider
- ELIXIR1
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Operation
- Rendering
- Allele calling3
- Exome variant detection3
- Genome variant detection3
- Germ line variant calling3
- Mutation detection3
- Somatic variant calling3
- Variant calling3
- Variant mapping3
- de novo mutation detection3
- Data handling2
- File handling2
- File processing2
- Processing2
- Report handling2
- Utility operation2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Cartography1
- Data visualisation1
- Differential splicing analysis1
- Mapping1
- Molecular visualisation1
- Plotting1
- Sequencing QC1
- Sequencing quality assessment1
- Sequencing quality control1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
- Visualisation1
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Event type
- Workshops and courses1
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Target audience
- Biologists
- Cette formation est destinée aux biologistes (ingénieurs, doctorants, chercheurs, enseignants-chercheurs, praticiens…) confrontés à l’analyse de données NGS, et qui ne disposent pas des compétences bioinformatiques suffisantes.2
- Beginners1
- Bioinformaticians1
- Bioinformaticians and Biologists who want to learn how to manipulate, process data, and make plots using R1
- Life Science Researchers1
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Eligibility
- Registration of interest1
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