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Content provider
- Australian BioCommons2
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Scientific topic
- RNA sequencing
- Data management4
- FAIR data4
- Findable, accessible, interoperable, reusable data4
- Metadata management4
- Pipelines3
- Software integration3
- Tool integration3
- Tool interoperability3
- Workflows3
- MicroRNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Transcriptome profiling2
- WTSS2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Bayesian methods1
- Bioinformatics1
- Biostatistics1
- Codon usage1
- DNA chips1
- DNA microarrays1
- Data analysis1
- Data architecture1
- Data architecture, analysis and design1
- Data design1
- Data rendering1
- Data visualisation1
- Descriptive statistics1
- Expression1
- Functional genomics1
- Gaussian processes1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Inferential statistics1
- Markov processes1
- Multivariate statistics1
- Omics1
- Phenomics1
- Probabilistic graphical model1
- Probability1
- Statistics1
- Statistics and probability1
- Transcription1
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Operation
- Analysis
- Data visualisation3
- Molecular visualisation3
- Plotting3
- Rendering3
- Visualisation3
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Expression analysis2
- Expression data analysis2
- 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
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- 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
- Variant analysis2
- Allele calling1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Differential expression analysis1
- Differential gene analysis1
- Differential gene expression analysis1
- Differential gene expression profiling1
- Differentially expressed gene identification1
- Exome variant detection1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses2
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Organizer
- Australian BioCommons2
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- Registration of interest2
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