Are you ready to explore the world of Next-Generation Sequencing (NGS) and advance your bioinformatics skills? Join BioCompiler’s comprehensive NGS: RNA-Seq Data Analysis Workshop and take a big leap in your scientific career! 🧬

Why RNA-Seq Matters?

RNA-Seq is a powerful tool in genomics that enables researchers to study gene expression, discover novel transcripts, and understand the biology behind diseases. Mastering RNA-Seq analysis will open opportunities worldwide in academia, industry, and research labs.

After completing this workshop, you will be able to:

• Understand RNA-Seq Basics: Grasp the fundamental principles of RNA-Seq and its applications in genomics research.
• Navigate R for Bioinformatics: Utilize R programming for data manipulation, visualization, and RNA-Seq analysis workflows.
• Master Bash for NGS Data: Efficiently handle large-scale NGS data using Bash, including file management, automation, and preprocessing.
• Perform Data Preprocessing: Execute key preprocessing steps, including quality control, trimming, and mapping of FASTQ files, to generate expression matrices.
• Conduct Downstream Analysis: Analyze differentially expressed genes (DEGs), perform enrichment analysis, and derive biological insights using R.
• Troubleshoot RNA-Seq Pipelines: Identify and resolve common challenges in RNA-Seq data analysis workflows.
• Apply Best Practices: Implement robust, reproducible workflows that align with industry and research standards.
• Complete Real-Life Projects: Work on practical case studies to reinforce skills and build confidence in RNA-Seq analysis.

This comprehensive skill set will prepare you to tackle real-world RNA-Seq projects in academia, industry, or research labs.