Training materials
-
WORKSHOP: Make your bioinformatics workflows findable and citable
Bioinformatics Workflows WorkflowHub FAIR Open Science
-
Video
EGA Submitter Portal Tutorial
Bioinformatics Genomics FEGA Federated EGA ELIXIR Converge
-
WORKSHOP: RNA-Seq: reads to differential genes and pathways
Bioinformatics Analysis Transcriptomics RNA-seq Workflows Nextflow nf-co.re
-
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
-
WEBINAR: Here's one we prepared earlier: (re)creating bioinformatics methods and workflows with Galaxy Australia
Bioinformatics Workflows FAIR Galaxy Australia
-
WEBINAR: Portable, reproducible and scalable bioinformatics workflows using Nextflow and Pawsey Nimbus Cloud
Bioinformatics Workflows Nextflow Containerisation
-
WORKSHOP: Single cell RNAseq analysis in R
Bioinformatics Analysis Transcriptomics R software Single cell RNAseq scRNAseq
-
WEBINAR: Getting started with whole genome mapping and variant calling on the command line
Genome mapping Variant calling Bioinformatics Workflows
-
WORKSHOP: R: fundamental skills for biologists
Data visualisation Data architecture, analysis and design Bioinformatics Analysis Statistics R software RStudio
-
WEBINAR: bio.tools - making it easier to find, understand and cite biological tools and software
Workflows Ontology and terminology Bioinformatics Research software EDAM FAIR