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Content provider
- ELIXIR Portugal1
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Operation
- Data handling
- Allele calling2
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Exome variant detection2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Genome variant detection2
- Germ line variant calling2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Mutation detection2
- 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
- Somatic variant calling2
- Transcript variant analysis2
- Variant analysis2
- Variant calling2
- Variant mapping2
- Visualisation2
- de novo mutation detection2
- Analysis1
- Classification1
- Clustering1
- Empirical Bayes1
- File handling1
- File processing1
- Mathematical modelling1
- Modelling and simulation1
- Principal component analysis1
- Processing1
- Report handling1
- Statistical inference1
- Statistical modelling1
- Utility operation1
- Variant pattern analysis1
- Variant prioritisation1
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Event type
- Workshops and courses1
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Country
- Portugal1
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Organizer
- Pedro Fernandes1
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Target audience
- Life Science Researchers1
- PhD students1
- post-docs1
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