bioRxivBioinformaticsPreprint
Integrative analysis and refined design of CRISPR knockout screens
Chen-Hao CheniD, Wei LiiD, Tengfei XiaoiD, Han XuiD, Peng JiangiD, Clifford A. MeyeriD, Myles A BrowniD, X. Shirley LiuiD
Abstract
Genome-wide CRISPR-Cas9 screen has been widely used to interrogate gene functions. However, the analysis remains challenging and rules to design better libraries beg further refinement. Here we present MAGeCK-NEST, which integrates protein-protein interaction (PPI), improves the inference accuracy when fewer guide-RNAs (sgRNAs) are available, and assesses screen qualities using information on PPI. MAGeCK-NEST also adopts a maximum-likelihood approach to remove sgRNA outliers, which are characterized with higher G-nucleotide counts, especially in regions distal from the PAM motif. Using MAGeCK-NEST, we found that choosing non-targeting sgRNAs as negative controls lead to strong bias, which can be mitigated by sgRNAs targeting the \"safe harbor\" regions. Custom-designed screens confirmed our findings, and further revealed that 19nt sgRNAs consistently gave the best signal-to-noise separation. Collectively, our method enabled robust calling of CRISPR screen hits and motivated the design of an improved genome-wide CRISPR screen library.
- assay: CRISPR screen
- research focus: variant effect prediction
- research focus: benchmarking
- approach: statistical model
- Citations
- 4
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Pooled CRISPR screening at high sensitivity with an empirically designed sgRNA library
Luisa Henkel, Benedikt Rauscher, … Michael Boutros·BMC BiologyPeer-reviewed·Nov 23, 2020
- A survey of multi-targeting and off-targeting sgRNAs across five genome-wide CRISPR-Cas9 knockout sgRNA libraries with GuideRefine
Stefanus Bernard, Michael D. Rainey, … Colm J. Ryan·bioRxiv·Aug 20, 2026
- Optimized parameters for Cas9 CRISPR interference library design
Smriti Srikanth, Fengyi Zheng, … John G. Doench·bioRxiv·Feb 26, 2026
- A benchmark comparison of CRISPRn guide-RNA design algorithms and generation of small single and dual-targeting libraries to boost screening efficiency
Sebastian Łukasiak, Alex T. Kalinka, … David Walter·BMC GenomicsPeer-reviewed·Feb 26, 2025
- JACKS: joint analysis of CRISPR/Cas9 knock-out screens
Felicity R. Allen, Fiona M. Behan, … Leopold Parts·Genome ResearchPeer-reviewed·Mar 1, 2019
- Reducing False Positives in CRISPR/Cas9 Screens from Copy Number Variations
Alexander Wu, Tengfei Xiao, … Wei Li·bioRxiv·Jan 11, 2018