- Home
- Events
Filter
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- Australian BioCommons87
- Galaxy Project4
- Show N_FILTERS more
-
-
-
Keyword
- Bioinformatics22
- Workflows13
- Nextflow8
- Genetic Variation6
- Human genomics5
- nf-core5
- AI4
- Data analysis4
- Galaxy4
- Galaxy Australia4
- HPC4
- Introductory4
- R4
- Variant calling4
- bioinformatics4
- Cloud computing3
- Containers3
- Deep learning3
- Genomics3
- Machine Learning and Artificial Intelligence Course3
- Spatial omics3
- Tools3
- Transcriptomics3
- life sciences3
- scRNAseq3
- Clinical genomics2
- Computational biology2
- Functional enrichment2
- Genes2
- Genetic variation2
- High performance computing2
- Life Science2
- Machine Learning2
- Microbiome2
- Multiomics2
- NCMAS2
- Protein biology2
- Proteins2
- RNASeq2
- Variant interpretation2
- WorkflowHub2
- data management2
- genome annotation2
- genome curation2
- phylogenetics2
- research software2
- workflows2
- Data sharing1
- sensitive data1
- Access management1
- Alphafold1
- Apollo1
- Artificial Inteligence1
- Artificial Intelligence1
- Beginner1
- Best Practices1
- BioCloud1
- BioSamples1
- Bioconductor1
- Bioplatforms Australia1
- CWL1
- Cancer1
- ChatGPT1
- Clinical Bioinformatics1
- Clinical data1
- Code-free1
- Coding1
- Command line1
- Computational research1
- Compute1
- Conservation genomics1
- Continuing education1
- Data Analysis1
- Data Integration1
- Data curation1
- Data privacy1
- Data skills1
- Data submission1
- Data visualisation1
- Databases1
- Demonstration1
- Distributed data analysis1
- Drug design1
- Education1
- Ethics1
- Evolution1
- FAIR1
- Functional analysis1
- GA4GH1
- Gene Expression1
- Gene expression1
- Genetic Outlier Analysi1
- Genetic variants1
- Genetics1
- Genome Sequencing1
- Genomic sequences1
- Global Biodata Coalition1
- Hybrid genome assembly1
- Infectious diseases1
- Life science1
- Show N_FILTERS more
-
-
-
Scientific topic
- Bioinformatics25
- Pipelines13
- Software integration13
- Tool integration13
- Tool interoperability13
- Workflows13
- Exomes12
- Genome annotation12
- Genomes12
- Genomics12
- Personal genomics12
- Synthetic genomics12
- Viral genomics12
- Whole genomes12
- DNA variation8
- Genetic variation8
- Genomic variation8
- Mutation8
- Polymorphism8
- Somatic mutations8
- Active learning6
- Data management6
- Ensembl learning6
- Kernel methods6
- Knowledge representation6
- Machine learning6
- Metadata management6
- MicroRNA sequencing6
- Neural networks6
- RNA sequencing6
- RNA-Seq6
- RNA-Seq analysis6
- Recommender system6
- Reinforcement learning6
- Research data management (RDM)6
- Small RNA sequencing6
- Small RNA-Seq6
- Small-Seq6
- Supervised learning6
- Transcriptome profiling6
- Unsupervised learning6
- WTSS6
- Whole transcriptome shotgun sequencing6
- miRNA-seq6
- Biomathematics5
- Computational biology5
- Mathematical biology5
- Omics5
- Theoretical biology5
- Comparative transcriptomics4
- Human genetics4
- Transcriptome4
- Transcriptomics4
- Aerobiology3
- Behavioural biology3
- Biological rhythms3
- Biological science3
- Biology3
- Chronobiology3
- Cryobiology3
- Genes3
- Genetics3
- Heredity3
- Open science3
- Phylogenetics3
- Protein bioinformatics3
- Protein databases3
- Protein informatics3
- Proteins3
- Reproductive biology3
- Algorithms2
- Bayesian methods2
- Biostatistics2
- Bottom-up proteomics2
- Cloud computing2
- Codon usage2
- Computer programming2
- Computer science2
- DNA chips2
- DNA microarrays2
- Data analysis2
- Data architecture2
- Data architecture, analysis and design2
- Data archival2
- Data archiving2
- Data curation2
- Data curation and archival2
- Data design2
- Data preservation2
- Data structures2
- Database curation2
- Descriptive statistics2
- Discovery proteomics2
- Expression2
- Gaussian processes2
- Gene expression2
- Gene expression profiling2
- Gene transcription2
- Gene translation2
- HPC2
- Show N_FILTERS more
-
-
-
Operation
- Allele calling5
- Data handling5
- Exome variant detection5
- File handling5
- File processing5
- Genome variant detection5
- Germ line variant calling5
- Mutation detection5
- Processing5
- Report handling5
- Somatic variant calling5
- Utility operation5
- Variant calling5
- Variant mapping5
- de novo mutation detection5
- Data analysis4
- Data visualisation2
- Functional genome annotation2
- Genome annotation2
- Metagenome annotation2
- Molecular visualisation2
- Plotting2
- Rendering2
- Structural genome annotation2
- Visualisation2
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Breakend assembly1
- Expectation maximisation1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Genome assembly1
- Genomic assembly1
- Gibbs sampling1
- Hypothesis testing1
- Omnibus test1
- Optimisation and refinement1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Sequence assembly (genome assembly)1
- Significance testing1
- Statistical analysis1
- Statistical calculation1
- Statistical test1
- Statistical testing1
- Show N_FILTERS more
-
-
-
Country
- Australia73
- Show N_FILTERS more
-
-
-
Target audience
- Biologists17
- bioinformaticians8
- Bioinformaticians3
- Life Science Researchers3
- Funders1
- Life scientists1
- Researchers1
- Service providers1
- The workshop is designed for anyone who is creating workflows, either via platforms like Galaxy Australia, or via the command line.1
- Show N_FILTERS more
-
-
-
Language
- English20
- Show N_FILTERS more
-
- Only show online events
- Show events from all spaces
- Hide past events
- Hide disabled events
- Show events with broken links