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Scientific topic
- DNA variation4
- Genetic variation4
- Genomic variation4
- Mutation4
- Polymorphism4
- Somatic mutations4
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- Personal genomics3
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- Bioinformatics2
- Chromosome walking2
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- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Genome sequencing2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
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- Panels2
- Primer walking2
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- WGS2
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- ChIP-exo1
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- ChIP-sequencing1
- Chip Seq1
- Chip sequencing1
- Chip-sequencing1
- MicroRNA sequencing1
- Pipelines1
- RNA sequencing1
- RNA-Seq1
- RNA-Seq analysis1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
- Software integration1
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- Tool interoperability1
- Transcriptome profiling1
- WTSS1
- Whole transcriptome shotgun sequencing1
- Workflows1
- miRNA-seq1
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Operation
- Variant calling
- Data handling41
- File handling41
- File processing41
- Processing41
- Report handling41
- Utility operation41
- Data brokering21
- Data deposition21
- Data deposition brokering21
- Data submission21
- Database deposition21
- Database submission21
- Data analysis10
- Allele calling6
- Data visualisation6
- Exome variant detection6
- Genome variant detection6
- Germ line variant calling6
- Molecular visualisation6
- Mutation detection6
- Plotting6
- Rendering6
- Somatic variant calling6
- Variant mapping6
- Visualisation6
- de novo mutation detection6
- Data formatting3
- Data reformatting3
- File format conversion3
- File formatting3
- File reformatting3
- Format conversion3
- Functional genome annotation3
- Genome annotation3
- Metagenome annotation3
- Structural genome annotation3
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data extraction2
- Data filtering2
- Data management planning2
- Data retrieval2
- Data retrieval (metadata)2
- Docking simulation2
- Expression analysis2
- Expression data analysis2
- File format validation2
- Format validation2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Macromolecular docking2
- Metadata retrieval2
- Metagenomic inference2
- Microarray data analysis2
- Molecular docking2
- Molecular surface 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
- Structure database search2
- 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
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- Workshops and courses6
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- Australia3
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