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Scientific topic
- Genomes
- Data management21
- Metadata management21
- Data curation10
- Database curation10
- Research data management (RDM)6
- Data archival5
- Data archiving5
- Data curation and archival5
- Data preservation5
- Data provenance5
- Data submission, annotation, and curation5
- FAIR data5
- Findable, accessible, interoperable, reusable data5
- Research data archiving5
- Data privacy2
- Data security2
- Biodiversity1
- Bioinformatics1
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- Data governance1
- Data integrity1
- Data quality1
- Data quality management1
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- Genomics1
- Personal genomics1
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- Whole genomes1
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Operation
- Data submission
- Allele calling3
- Data visualisation3
- Exome variant detection3
- Functional genome annotation3
- Genome annotation3
- Genome variant detection3
- Germ line variant calling3
- Metagenome annotation3
- Molecular visualisation3
- Mutation detection3
- Plotting3
- Rendering3
- Somatic variant calling3
- Structural genome annotation3
- Variant calling3
- Variant mapping3
- Visualisation3
- de novo mutation detection3
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data handling2
- Expression analysis2
- Expression data analysis2
- File handling2
- File processing2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation 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
- Processing2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Report handling2
- Sequence alignment2
- Sequence alignment (constrained)2
- Sequence alignment construction2
- Sequence alignment generation2
- Sequence read pre-processing2
- Sequence variation analysis2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Transcript variant analysis2
- Utility operation2
- Variant analysis2
- Breakend assembly1
- Data deposition1
- Database deposition1
- Database submission1
- Deposition1
- Genome assembly1
- Genomic assembly1
- Optimisation and refinement1
- Sequence assembly (genome assembly)1
- Submission1
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Event type
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- Oslo1
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- Norway1
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Eligibility
- First come first served1
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