MAGeCK enables robust identification of essential genes from genome-scale CRISPR/Cas9 knockout screens

Wei Li(Dana-Farber Cancer Institute), Han Xu(Dana-Farber Cancer Institute), Tengfei Xiao(Dana-Farber Cancer Institute), Le Cong(Broad Institute), Michael I. Love(Dana-Farber Cancer Institute), Feng Zhang(Broad Institute), Rafael A. Irizarry(Dana-Farber Cancer Institute), Jun S. Liu(Harvard University), Myles Brown(Brigham and Women's Hospital), X. Shirley Liu(Dana-Farber Cancer Institute)
Genome biology
December 4, 2014
Cited by 2,764Open Access
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Abstract

We propose the Model-based Analysis of Genome-wide CRISPR/Cas9 Knockout (MAGeCK) method for prioritizing single-guide RNAs, genes and pathways in genome-scale CRISPR/Cas9 knockout screens. MAGeCK demonstrates better performance compared with existing methods, identifies both positively and negatively selected genes simultaneously, and reports robust results across different experimental conditions. Using public datasets, MAGeCK identified novel essential genes and pathways, including EGFR in vemurafenib-treated A375 cells harboring a BRAF mutation. MAGeCK also detected cell type-specific essential genes, including BCR and ABL1, in KBM7 cells bearing a BCR-ABL fusion, and IGF1R in HL-60 cells, which depends on the insulin signaling pathway for proliferation.


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