Training materials
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WORKSHOP: Make your bioinformatics workflows findable and citable
Bioinformatics Workflows WorkflowHub FAIR Open Science
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WORKSHOP: RNA-Seq: reads to differential genes and pathways
Bioinformatics Analysis Transcriptomics RNA-seq Workflows Nextflow nf-co.re
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WEBINAR: Variant interpretation: from the clinic to the lab… and back again
Clinical genomics Variant interpretation Variant curation Continuing Professional Development Professional Development Bioinformatics Genomics Variant calling
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WEBINAR: Here's one we prepared earlier: (re)creating bioinformatics methods and workflows with Galaxy Australia
Bioinformatics Workflows FAIR Galaxy Australia
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WEBINAR: Effective, inclusive, and scalable training in the life sciences, clinical education and beyond
Short-format training Clinical education Continuing education Professional development Training Lifelong learning Pedagogy
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WEBINAR: Portable, reproducible and scalable bioinformatics workflows using Nextflow and Pawsey Nimbus Cloud
Bioinformatics Workflows Nextflow Containerisation
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WORKSHOP: Single cell RNAseq analysis in R
Bioinformatics Analysis Transcriptomics R software Single cell RNAseq scRNAseq
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WEBINAR: Getting started with whole genome mapping and variant calling on the command line
Genome mapping Variant calling Bioinformatics Workflows
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WEBINAR: bio.tools - making it easier to find, understand and cite biological tools and software
Workflows Ontology and terminology Bioinformatics Research software EDAM FAIR
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WORKSHOP: R: fundamental skills for biologists
Data visualisation Data architecture, analysis and design Bioinformatics Analysis Statistics R software RStudio