Learn how to process and interpret functional genomic perturbation screens using CRISPR and RNAi technologies. This module walks through pooled and arrayed screen design, NGS-based readouts, raw count processing, normalization, hit calling, enrichment analysis, and causal interpretation using pathways and networks. You will implement hands-on workflows in Python/R inspired by tools like MAGeCK, and convert screen results into mechanistic and actionable hypotheses for drug discovery and systems biology.