A Practical Introduction to NGS Data Analysis and Variant Calling
From Quality Control and Read Mapping to DNA Variant Calling (VCF)
Date: 22 - 24 March 2027
Timezone: Berlin
Language of instruction: English
This workshop gives you a practical introduction to Next-Generation Sequencing (NGS), with a clear focus on the bioinformatics decisions that determine whether an analysis is trustworthy.
You will learn how to assess your own NGS data, identify common problems and sources of error, and complete a first analysis workflow that includes DNA variant calling.
During the course, you will work with a real Illumina NGS dataset and use widely adopted open-source tools.
Contact: ecSeq Bioinformatics GmbH Sternwartenstr. 29 D-04103 Leipzig Germany Email: [email protected]
Keywords: DNA-seq, RNA-seq, Variant calling, BIoinformatics
Venue: cmt GmbH, Hansastraße 32, 80686 Munich, Germany
City: München
Country: Germany
Postcode: 80686
Organizer: ecSeq Bioinformatics GmbH
Eligibility:
- First come first served
Target audience: Biological sciences research students and postdocs who may want to use HPC in their research.Please note that Biochemistry first year graduate students book this course via their Moodle site not here., Biologists, Pathologists, Molecular Biologists, medical scientists
Capacity: 20
Event types:
- Workshops and courses
Cost basis: Cost incurred by all
Cost: € 989.0 (EUR)
Activity log
