NGS Data Analysis Tutorials & Complete Workflow Graph

Interactive, top-to-bottom architectural blueprint of the Next-Generation Sequencing (NGS) computational workflow. The process progresses sequentially from instrument data generation and FASTQ quality filtering, through reference genome alignment and BAM duplicate removal, branching into specialized multi-omic pipelines (Variant Calling, Transcriptomics, Single-Cell, Epigenomics, Metagenomics), and culminating in functional annotation and interactive biological visualization.

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