NGS & Linux Workflow: DNA-Seq Data Analysis - recorded course

In the era of Big Data genomics, the ability to navigate the Linux terminal is the ultimate superpower for researchers. This specialized course, DNASeq + Linux, provides a hands-on immersion into the computational backbone of Next-Generation Sequencing (NGS) analysis. You will move beyond simple point-and-click interfaces, learning to manage directories, handle large FASTQ files, and execute multi-tool pipelines in a high-performance computing environment. We integrate Artificial Intelligence (AI) through intelligent terminal assistants that help optimize your Bash scripting and debug complex bioinformatics errors in real-time. The curriculum follows a rigorous DNA-Seq workflow—from quality control and reference genome alignment to AI-accelerated variant calling. By mastering the command-line interface (CLI), you will learn how to automate repetitive tasks and ensure your research is scalable and reproducible. Whether you are aiming for a career in Genomics, Precision Medicine, or Biotechnology, this course provides the technical grit required to lead in the digital laboratory.