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Content provider
- NBIS3
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Operation
- File formatting
- Data handling41
- File handling41
- File processing41
- Processing41
- Report handling41
- Utility operation41
- Data deposition21
- Data submission21
- Database deposition21
- Database submission21
- Deposition21
- Submission21
- Analysis9
- Allele calling7
- Exome variant detection7
- Genome variant detection7
- Germ line variant calling7
- Mutation detection7
- Somatic variant calling7
- Variant calling7
- Variant mapping7
- de novo mutation detection7
- Data visualisation6
- Molecular visualisation6
- Plotting6
- Rendering6
- Visualisation6
- File format conversion3
- File reformatting3
- Format conversion3
- Formatting3
- Reformatting3
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data extraction2
- Data retrieval2
- Data retrieval (metadata)2
- Expression analysis2
- Expression data analysis2
- File format validation2
- Filtering2
- Format validation2
- Functional genome annotation2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Genome annotation2
- Metadata retrieval2
- Metagenome annotation2
- Metagenomic inference2
- Microarray data analysis2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Retrieval2
- Sequence alignment2
- Sequence alignment (constrained)2
- Sequence alignment construction2
- Sequence alignment generation2
- Sequence filtering2
- Sequence read pre-processing2
- Sequence variation analysis2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Structural genome annotation2
- Transcript variant analysis2
- Variant analysis2
- rRNA filtering2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Annotation1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Breakend assembly1
- Cartography1
- Classification1
- Clustering1
- Design1
- Differential expression analysis1
- Differential gene analysis1
- Differential gene expression analysis1
- Differential gene expression profiling1
- Differential splicing analysis1
- Differentially expressed gene identification1
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Event type
- Workshops and courses3
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Country
- Sweden2
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Target audience
- PhD candidates3
- Researchers3
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Eligibility
- Registration of interest3
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