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Content provider
- Australian BioCommons3
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Operation
- Allele calling
- 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
- Rendering1
- 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 courses3
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Country
- Australia3
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Organizer
- Australian BioCommons3
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Target audience
- Biologists
- bioinformaticians3
- Biologists and bioinformaticians who are dealing with high-throughput gene expression data or other high-throughput data and would like to learn state-of-the-art methods for mining and analysing such data.1
- 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.1
- oncologists1
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Eligibility
- Registration of interest3
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