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Content provider
- Australian BioCommons1
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Scientific topic
- Bioinformatics1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- 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
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Operation
- Genome variant detection
- Data handling17
- File handling17
- File processing17
- Processing17
- Report handling17
- Utility operation17
- Data deposition8
- Data submission8
- Database deposition8
- Database submission8
- Deposition8
- Submission8
- Analysis7
- Data visualisation3
- Molecular visualisation3
- Plotting3
- Rendering3
- Visualisation3
- Allele calling1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Exome variant detection1
- Expectation maximisation1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Germ line variant calling1
- Gibbs sampling1
- Hypothesis testing1
- Mutation detection1
- Omnibus test1
- Optimisation and refinement1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Significance testing1
- Somatic variant calling1
- Statistical analysis1
- Statistical calculation1
- Statistical test1
- Statistical testing1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses1
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Organizer
- Australian BioCommons1
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Eligibility
- First come first served1
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