- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- ELIXIR Norway9
- Show N_FILTERS more
-
-
-
Scientific topic
- Data clean-up5
- Data cleaning5
- Data curation5
- Data governance5
- Data identity and mapping5
- Data integrity5
- Data provenance5
- Data quality5
- Data quality management5
- Data stewardship5
- Data submission, annotation, and curation5
- Database curation5
- Pipelines5
- Software integration5
- Tool integration5
- Tool interoperability5
- Workflows5
- Data management4
- Metadata management4
- Show N_FILTERS more
-
-
-
Operation
- Data handling
- File handling9
- File processing9
- Processing9
- Report handling9
- Utility operation9
- Data deposition4
- Data submission4
- Database deposition4
- Database submission4
- Deposition4
- Submission4
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Expression analysis2
- Expression data analysis2
- 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
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Rendering2
- 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
- Variant analysis2
- Visualisation2
- Allele calling1
- Annotation1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses9
- Show N_FILTERS more
-
-
-
Country
- Norway9
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events