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This skill integrates the deepTools suite into the Claude environment, providing a specialized toolkit for processing Next-Generation Sequencing (NGS) data. It enables researchers to convert BAM alignments into normalized coverage tracks, perform rigorous quality control checks like fingerprinting and correlation, and generate publication-quality heatmaps and profile plots. Designed for ChIP-seq, RNA-seq, and ATAC-seq workflows, it streamlines complex genomic analyses by providing standardized command-line patterns, effective genome size references, and visualization best practices.