Munich, Germany | September 9–11, 2026
A Practical Introduction to NGS Data Analysis and Variant Calling
Do you work with sequencing data but still feel that parts of the analysis pipeline remain a black box?
In this hands-on workshop, participants learn how to move from raw FASTQ files to DNA variants step by step. We cover quality control, read mapping, BAM/VCF files, variant calling, result interpretation, and common pitfalls using real Illumina sequencing data. No prior bioinformatics experience is required.
Small group, extensive practical exercises, and plenty of time for questions make this one of our most popular introductory courses for biologists and life scientists.
More information: Website
A Practical Introduction to NGS Data Analysis and Variant Calling
Do you work with sequencing data but still feel that parts of the analysis pipeline remain a black box?
In this hands-on workshop, participants learn how to move from raw FASTQ files to DNA variants step by step. We cover quality control, read mapping, BAM/VCF files, variant calling, result interpretation, and common pitfalls using real Illumina sequencing data. No prior bioinformatics experience is required.
Small group, extensive practical exercises, and plenty of time for questions make this one of our most popular introductory courses for biologists and life scientists.
More information: Website