This 3-day beginner-friendly workshop introduces participants to the fundamentals of Next-Generation Sequencing (NGS) data processing and interpretation. Participants will learn how sequencing data is generated, what raw FASTQ files contain, how quality control is performed, and how cleaned data can be interpreted for biological research.
The workshop is designed to give learners a practical foundation in NGS workflows, including raw data understanding, quality assessment, read preprocessing, basic alignment awareness, and result interpretation. Through live demonstrations and guided hands-on activities, participants will explore commonly used tools and file formats used in genomics and bioinformatics research.
This workshop is suitable for students, researchers, PhD scholars, academicians, and life science professionals who want to begin learning NGS data analysis in a structured and practical way.
