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Content provider
- Australian BioCommons1
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Scientific topic
- Bioinformatics2
- Bayesian methods1
- Biostatistics1
- Cloud computing1
- Computer science1
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Operation
- Data handling
- Allele calling3
- Exome variant detection3
- Genome variant detection3
- Germ line variant calling3
- Mutation detection3
- Somatic variant calling3
- Variant calling3
- Variant mapping3
- de novo mutation detection3
- File handling2
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- Utility operation2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Cartography1
- Data visualisation1
- Differential splicing analysis1
- Mapping1
- Molecular visualisation1
- Plotting1
- Rendering1
- Sequencing QC1
- Sequencing quality assessment1
- Sequencing quality control1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
- Visualisation1
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Event type
- Workshops and courses2
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Venue
- Online1
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Country
- Australia1
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Target audience
- Biologists
- Researchers9
- PhD candidate7
- All postgraduates6
- PhD students6
- Professors6
- data steward / data manager6
- Life sciences5
- Senior scientist/ Principal investigator5
- PhD candidates4
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- postdoctoral researchers3
- data manager2
- rare disease patients representatives1
- Bioinformaticians1
- Bioinformaticians and Biologists who want to learn how to manipulate, process data, and make plots using R1
- Clinicians1
- Life Scientists1
- Master students1
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- post-docs1
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