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  • ecSeq Bioinformatics
    Senior Member
    • May 2012
    • 499

    #1

    Last call: In-person NGS data analysis & variant calling workshop (Munich, Feb 24–26, 2026)

    We are running a 3-day, in-person introductory workshop on NGS data analysis and DNA variant calling, and registration will close shortly.

    A Practical Introduction to NGS Data Analysis and Variant Calling

    February 24–26, 2026

    Munich, Germany

    Language: English

    Apply: Website

    The workshop is aimed at molecular biologists and life scientists who work with sequencing data and want to better understand — and independently run — the essential first analysis steps.

    Topics covered
    • quality control of FASTQ files and identification of common pitfalls
    • preprocessing (adapter and quality trimming) and why these steps matter
    • read mapping and interpretation of SAM/BAM files
    • inspection of alignments in genome browsers (IGV/UCSC)
    • DNA variant calling, VCF format, and basic filtering/interpretation

    The course combines short lectures with extensive hands-on exercises. Participants work at individual workstations, and trainers are available throughout for questions and live troubleshooting.

    Practical details
    • Dates: February 24–26, 2026 (9:00–17:00)
    • Location: Munich, Germany
    • Format: Small-group, fully hands-on, in-person

    More details and registration: Website

    Click image for larger version

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    ecSeq Bioinformatics is Europe’s leading provider of hands-on bioinformatics workshops and professional data analysis in the field of Next-Generation Sequencing (NGS).

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