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DTSTAMP:20260804T231327Z
UID:0c72a21d-a459-44e2-b0e2-54aaac986396
DTSTART:20260909T070000Z
DTEND:20260911T150000Z
DESCRIPTION:This workshop is designed to give you a solid\, practical under
 standing of Next-Generation Sequencing (NGS) with a clear focus on the bio
 informatics steps that most often determine whether an analysis is trustwo
 rthy.\n\nYou will learn how to assess your own NGS data\, identify common 
 problems and error sources\, and complete a first downstream analysis work
 flow\, including DNA variant calling.\n\nIn the course we work with a real
 -life Illumina NGS dataset.\n\nAfter 3 days\, you will be able to:\n- Eval
 uate raw sequencing data (FASTQ) using quality control best practices\n- P
 erform preprocessing (adapter clipping\, quality trimming) and understand 
 why you do it\n- Map reads to a reference genome and interpret mapping qua
 lity (SAM/BAM)\n- Inspect alignments in IGV/UCSC to validate findings\n- G
 enerate and interpret a VCF\, apply basic filtering\, and avoid common pit
 falls
LOCATION:cmt GmbH\, Hansastraße 32\, 80686 Munich\, Germany
SUMMARY:A Practical Introduction to NGS Data Analysis and Variant Calling
URL;VALUE=URI:https://www.ecseq.com/workshops/workshop_2026-07-NGS-Next-Gen
 eration-Sequencing-Data-Analysis-A-Practical-Introduction
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