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Scientific topic
- Bioinformatics
- Biological sequences1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Primer walking1
- Sanger sequencing1
- Sequence analysis1
- Sequence databases1
- Sequences1
- Sequencing1
- Targeted next-generation sequencing panels1
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Operation
- Mapping
- Allele calling2
- Data handling2
- Exome variant detection2
- File handling2
- File processing2
- Genome variant detection2
- Germ line variant calling2
- Mutation detection2
- Processing2
- Report handling2
- Somatic variant calling2
- Utility operation2
- Variant calling2
- Variant mapping2
- de novo mutation detection2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Analysis1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Cartography1
- Data visualisation1
- Database search1
- Differential splicing analysis1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Molecular visualisation1
- Optimisation and refinement1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Plotting1
- Rendering1
- Search1
- Sequencing QC1
- Sequencing quality assessment1
- Sequencing quality control1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
- Variant pattern analysis1
- Variant prioritisation1
- Visualisation1
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- Workshops and courses1
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- Germany1
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