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Content provider
- Australian BioCommons1
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Keyword
- RNA-seq
- Data analysis5
- Data preserving3
- Data sharing3
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- Bioinformatics2
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- CWL1
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Scientific topic
- Bioinformatics1
- Codon usage1
- DNA chips1
- DNA microarrays1
- Expression1
- Functional genomics1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- MicroRNA sequencing1
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- RNA-Seq analysis1
- Small RNA sequencing1
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- Software integration1
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- Transcription1
- Transcriptome profiling1
- WTSS1
- Whole transcriptome shotgun sequencing1
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Operation
- Analysis
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- 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
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Plotting2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Rendering2
- 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
- Visualisation2
- Allele calling1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- 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 courses1
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Organizer
- Australian BioCommons1
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- Registration of interest1
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