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Introduction to NGS Technologies → Result Reporting and Interpretation
This learning path guides bioinformatics students through building and executing a complete Next-Generation Sequencing (NGS) data analysis pipeline, from raw FASTQ files to annotated variants. It covers quality control, alignment, post-alignment processing, variant calling, annotation, and reporting, emphasizing practical skills and conceptual understanding.
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13 steps · 3 stages. Click any step to inspect it and see it on the Path Map.
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