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This 5-Day Practical Course: Raw FASTQ Files to Gene Count Matrix Using Linux & Bioinformatics Tools provides hands-on training in RNA sequencing (RNA-Seq) data processing, from raw sequencing files to an analysis-ready gene count matrix. Participants will learn Linux commands, FASTQ data downloading from NCBI SRA, quality assessment using FastQC, read trimming with fastp, sequence alignment using HISAT2, and gene quantification using featureCounts. Through real datasets and step-by-step practical exercises, learners will develop the skills needed to build and execute a complete RNA-Seq preprocessing pipeline. This beginner-friendly course is ideal for undergraduate and postgraduate students, PhD scholars, researchers, and bioinformatics professionals who want to gain practical experience in next-generation sequencing (NGS) data analysis.
Course Title: Raw FASTQ Files to Gene Count Matrix Using Linux & Bioinformatics Tools
Duration: 5 Days
Course Level: Beginner
Category: Bioinformatics / RNA-Seq / NGS Data Analysis
Course Format: Online Practical Training
Language: English
Prerequisites: No prior knowledge of Linux or bioinformatics required
Operating System: Windows 10/11 (using WSL2 or Ubuntu Linux)
Required Equipment: Laptop or desktop computer with a stable internet connection
Software & Tools: Ubuntu Linux, Conda, SRA Toolkit, FastQC, fastp, HISAT2, SAMtools, and featureCounts
Practical Training: Real RNA-Seq datasets from NCBI SRA
Final Output: Quality-controlled sequencing reads, aligned BAM files, and an analysis-ready gene count matrix
Target Audience: BS, MSc, MPhil, PhD students, postdoctoral researchers, biologists, geneticists, and bioinformatics enthusiasts
Laptop or Computer: Windows 10/11 with at least 8 GB RAM (16 GB recommended).
Internet Connection: Stable internet access for downloading software, tools, and RNA-Seq datasets.
Operating System: Windows with WSL2 (Ubuntu Linux) or a computer running Ubuntu Linux.
Software Installation: All required bioinformatics tools will be installed during the course with step-by-step guidance.
Prior Knowledge: No previous experience in Linux, programming, RNA-Seq, or bioinformatics is required.
Educational Background: Basic understanding of biology or genetics is helpful but not mandatory.
Learning Commitment: Willingness to participate in practical exercises and work with real sequencing datasets.
Storage Space: At least 30–50 GB of free disk space recommended for software installation and practice datasets.
This course is designed for students, researchers, and professionals who want to develop practical skills in RNA-Seq data processing using Linux and bioinformatics tools.
Undergraduate Students: BS/BSc students in biology, biotechnology, genetics, and related disciplines.
Postgraduate Students: MSc, MPhil, and PhD scholars working with molecular biology, genomics, and transcriptomics.
Postdoctoral Researchers: Researchers interested in applying RNA-Seq data processing techniques to their scientific projects.
Biologists and Geneticists: Professionals seeking practical experience in next-generation sequencing (NGS) data analysis.
Bioinformatics Beginners: Individuals with no prior experience in Linux or RNA-Seq analysis.
Research Scientists: Professionals working in plant sciences, agriculture, microbiology, biomedical sciences, and molecular genetics.
Data Analysts: Individuals interested in expanding their skills into genomics and computational biology.
No prior programming or Linux experience is required. The course starts with fundamental concepts and progresses to a complete practical RNA-Seq preprocessing workflow.
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