- Home
- Events
Filter
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- Australian BioCommons2
- Show N_FILTERS more
-
-
-
Scientific topic
- Genomes
- Data management27
- Metadata management27
- Research data management (RDM)27
- Data archival16
- Data archiving16
- Data curation16
- Data curation and archival16
- Data preservation16
- Database curation16
- Research data archiving16
- FAIR data9
- Findable, accessible, interoperable, reusable data9
- Data governance7
- Data clean-up6
- Data cleaning6
- Data identity and mapping6
- Data integrity6
- Data quality6
- Data quality management6
- Pipelines6
- Software integration6
- Tool integration6
- Tool interoperability6
- Workflows6
- Data privacy3
- Data security3
- Bayesian methods2
- Bioinformatics2
- Biostatistics2
- Data analysis2
- Data architecture2
- Data architecture, analysis and design2
- Data design2
- Data rendering2
- Data visualisation2
- Descriptive statistics2
- Exomes2
- Gaussian processes2
- Genome annotation2
- Genomics2
- Inferential statistics2
- Markov processes2
- Multivariate statistics2
- Personal genomics2
- Probabilistic graphical model2
- Probability2
- Statistics2
- Statistics and probability2
- Synthetic genomics2
- Viral genomics2
- Whole genomes2
- Ancient DNA1
- Biological sequences1
- Chromosomes1
- Cloud computing1
- Computer science1
- DNA1
- DNA analysis1
- Data integration1
- Data integration and warehousing1
- Data warehousing1
- HPC1
- High performance computing1
- High-performance computing1
- Human genetics1
- Omics1
- Rare diseases1
- Sequence analysis1
- Sequence databases1
- Show N_FILTERS more
-
-
-
Operation
- Data handling
- Allele calling3
- Data visualisation3
- Exome variant detection3
- Functional genome annotation3
- Genome annotation3
- Genome variant detection3
- Germ line variant calling3
- Metagenome annotation3
- Molecular visualisation3
- Mutation detection3
- Plotting3
- Rendering3
- Somatic variant calling3
- Structural genome annotation3
- Variant calling3
- Variant mapping3
- Visualisation3
- de novo mutation detection3
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Expression analysis2
- Expression data analysis2
- File handling2
- File processing2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Processing2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Report handling2
- 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
- Utility operation2
- Variant analysis2
- Breakend assembly1
- Data brokering1
- Data deposition1
- Data deposition brokering1
- Data submission1
- Database deposition1
- Database submission1
- Genome assembly1
- Genomic assembly1
- Optimisation and refinement1
- Sequence assembly (genome assembly)1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses2
- Show N_FILTERS more
-
-
-
Venue
- Online1
- Show N_FILTERS more
-
-
-
Country
- Australia2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events