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WEBINAR: Getting started with command line bioinformatics
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WORKSHOP: Variant calling in humans, animals and plants with Galaxy
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WEBINAR: Detection of and phasing of hybrid accessions in a target capture dataset
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WEBINAR: Getting started with deep learning
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WEBINAR: Making sense of phosphoproteomics data with Phosphomatics
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WEBINAR: Conflict in multi-gene datasets: why it happens and what to do about it - deep coalescence, paralogy and reticulation
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Presentation
Make your computational workflows findable and citable: WorkflowHub BYOW workshop
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WORKSHOP: Introduction to Metabarcoding using QIIME2
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WEBINAR: Managing hands-on data analysis training with Galaxy
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WORKSHOP: Unlocking nf-core - customising workflows for your research
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WEBINAR: Protection of genomic data and the Australian Privacy Act: when is genomic data 'personal information'?
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WEBINAR: Variant interpretation: from the clinic to the lab… and back again
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WEBINAR: Where to go when your bioinformatics outgrows your compute
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WORKSHOP: Hybrid de novo genome assembly
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WEBINAR: Getting started with command line bioinformatics
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WORKSHOP: Machine learning in the life sciences
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WEBINAR: No code, no problem - data analysis for biologists with Galaxy Australia
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WEBINAR: Making sense of phosphoproteomics data with Phosphomatics
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WORKSHOP: RNASeq: reads to differential genes and pathways
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WEBINAR: Getting started with RNAseq: Transforming raw reads into biological insights
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WEBINAR: DOME - Machine Learning Best Practices & Recommendations
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WORKSHOP: RNA-Seq: reads to differential genes and pathways
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WORKSHOP: Introduction to Machine Learning in R - from data to knowledge
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WEBINAR: Scaling up bioinformatics with ABLeS, the Australian BioCommons Leadership Share
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WORKSHOP: Translating workflows into Nextflow with Janis
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WORKSHOP: RNAseq: reads to differential expression
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WEBINAR: Building the future of bioinformatics with Nextflow: Technical innovation, community engagement, and career development opportunities
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WEBINAR: MetaboLights: the home for metabolomics experiments and derived information
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WEBINAR: BioSamples: supporting multi-omics data integration with FAIR sample records
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WORKSHOP: Genetic Outlier Analysis
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