17/08/2026
Working with sequencing data, but would like to understand the analysis a little better?
At ecSeq Bioinformatics, we offer practical NGS data analysis workshops for researchers who want to become more confident working with their own data.
Many of our participants are PhD students, postdocs, wet-lab scientists or researchers from biology and medicine who use NGS in their projects, but are not necessarily trained bioinformaticians.
In our courses, we work hands-on with real sequencing data and commonly used bioinformatics tools. Depending on the workshop, topics include Variant Calling, RNA-Seq, Single-Cell RNA-Seq, Epigenomics, Nextflow and the basics of working with NGS data on the command line.
The important part for us is that participants do not just learn which commands to run. We want them to understand what happens during the analysis, how to evaluate data quality, where problems can occur and how to judge whether a result actually makes sense.
Some of our courses start from the basics, so previous bioinformatics experience is not always required.
You can find our current NGS data analysis workshops here:
www.ecseq.com/ngs-workshops
