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Content provider
- NBIS2
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Operation
- Format validation
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data deposition2
- Data handling2
- Data submission2
- Data visualisation2
- Database deposition2
- Database submission2
- Deposition2
- Expression analysis2
- Expression data analysis2
- File format conversion2
- File format validation2
- File formatting2
- File handling2
- File processing2
- File reformatting2
- Filtering2
- Format conversion2
- Formatting2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Plotting2
- Processing2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Reformatting2
- Rendering2
- Report handling2
- 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
- Submission2
- Transcript variant analysis2
- Utility operation2
- Variant analysis2
- Visualisation2
- rRNA filtering2
- Allele calling1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses2
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Country
- Sweden1
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Organizer
- NBIS2
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Sponsor
- ELIXIR-CONVERGE2
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Target audience
- PhD candidates2
- Researchers2
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Eligibility
- Registration of interest2
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