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Content provider
- Australian BioCommons1
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Scientific topic
- DNA-Seq
- DNA variation2
- Genetic variation2
- Genomic variation2
- Mutation2
- Polymorphism2
- Somatic mutations2
- Bioinformatics1
- Chromosome walking1
- Clone verification1
- DNase-Seq1
- De novo genome sequencing1
- Exomes1
- Genome annotation1
- Genome sequencing1
- Genomes1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Personal genomics1
- Pipelines1
- Primer walking1
- Sanger sequencing1
- Sequencing1
- Software integration1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Tool integration1
- Tool interoperability1
- Viral genomics1
- WGS1
- Whole genome resequencing1
- Whole genome sequencing1
- Whole genomes1
- Workflows1
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Operation
- Variant mapping
- Allele calling1
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Cartography1
- Differential splicing analysis1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mapping1
- Mutation detection1
- Optimisation and refinement1
- Sequencing QC1
- Sequencing quality assessment1
- Sequencing quality control1
- Somatic variant calling1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
- Variant calling1
- de novo mutation detection1
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Event type
- Workshops and courses1
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