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An unbiased survey of distal element-gene regulatory interactions with direct-capture targeted Perturb-seq

GSE303901 Homo sapiens Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other 97 samples 2025/08/15 GPL34281GPL18573
Summary
We developed Direct-Capture Targeted Perturb-seq (DC-TAP-seq), a cost-effective and sensitive approach that integrates U6-driven guide RNA capture with TAP-seq, enabling high-throughput screening of thousands of E–G connections at lower read depth. We applied this method to perform unbiased enhancer screens in two human cell types, K562 and WTC11. Our dataset revealed novel classes of non-canonical cis-regulatory elements (CREs) that were under-sampled in previous CRISPRi screens
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NCBI GEO page ↗ Paper (PMID 41000760) ↗ {# Names what the click gives you. "Open in finder" meant nothing to a visitor who arrived from a search engine and has never seen the tool. #} Find more human RNA-seq datasets →
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