Training materials
Difficulty level: Not specified
and Authors: Beecroft, Sarah (orcid: 0000-0002-3935-2279) or Christopher Barnett or Gary Bader or Wolfgang Maier or erasche
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WORKSHOP: Unlocking nf-core - customising workflows for your research
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WEBINAR: Pro tips for scaling bioinformatics workflows to HPC
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WORKSHOP: RNA-Seq: reads to differential genes and pathways
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hands-on tutorial
Hands-on for 'Somatic Variant Discovery from WES Data Using Control-FREEC' tutorial
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WEBINAR: Portable, reproducible and scalable bioinformatics workflows using Nextflow and Pawsey Nimbus Cloud
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hands-on tutorial
Hands-on for 'Mapping and molecular identification of phenotype-causing mutations' tutorial
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hands-on tutorial
Hands-on for 'Exome sequencing data analysis for diagnosing a genetic disease' tutorial
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hands-on tutorial
Hands-on for 'Identification of somatic and germline variants from tumor and normal sample pairs' tutorial
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hands-on tutorial
Hands-on for 'Trio Analysis using Synthetic Datasets from RD-Connect GPAP' tutorial
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hands-on tutorial
Hands-on for 'Pre-processing of Single-Cell RNA Data' tutorial