bioRxivGenomicsPreprint
Systematic identification of seed-driven off-target effects in Perturb-seq experiments
Austin HartmaniD, John D. BlairiD, Thao P. Nguyen, Kyle A. DysoniD, Alexandra BraduiD, Oliver Takacsi-Nagy, Katherine E. Santostefano, Theresa Boade, Matthew Bolaños, Ronghui ZhuiD, Emma DanniD, Alexander MarsoniD, Aaron D. GitleriD, Rahul SatijaiD, Ansuman T. SatpathyiD, Theodore L. RothiD
Abstract
Genome-wide Perturb-seq (GWPS) has emerged as a powerful approach for unbiased mapping of gene regulatory networks. A key assumption underlying many Perturb-seq analyses is that each guide RNA exclusively perturbs a single target locus. Without methods to identify and filter off-target events, erroneous gene-pathway associations driven by off-target activity can propagate into downstream analyses. Here, we present a workflow for the systematic identification of candidate off-target events in CRISPRi Perturb-seq experiments. Our approach exploits the observation that cells harboring a guide which represses an off-target gene display transcriptional similarity to cells in which that gene is directly targeted by an on-target guide. We apply our workflow to multiple GWPS datasets and nominate off-target events in which a guide nominally targeting one gene also represses a distinct gene producing a phenotype likely attributable to the off-target perturbation. We use both off-target gene repression and guide seed sequence alignments at the off-target promoter locus as evidence for off-target effects and find independent evidence of putative off-target events in separate GWPS datasets. Together, these results establish a principled framework for the identification and filtering of off-target guide effects in Perturb-seq experiments.
- organism: human
- assay: CRISPR screen
- research focus: differential expression
- approach: statistical model
- Citations
- 2
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