Li Wei, Xu Han, Xiao Tengfei, Cong Le, Love Michael I, Zhang Feng, Irizarry Rafael A, Liu Jun S, Brown Myles, Liu X Shirley
Genome Biol. 2014;15(12):554. doi: 10.1186/s13059-014-0554-4.
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.
我们提出了基于模型的全基因组CRISPR/Cas9敲除分析(MAGeCK)方法,用于在全基因组规模的CRISPR/Cas9敲除筛选中对单向导RNA、基因和通路进行优先级排序。与现有方法相比,MAGeCK表现出更好的性能,能同时识别正向和负向选择的基因,并在不同实验条件下报告可靠的结果。利用公开数据集,MAGeCK识别出了新的必需基因和通路,包括在携带BRAF突变的维莫非尼处理的A375细胞中的EGFR。MAGeCK还在携带BCR-ABL融合的KBM7细胞中检测到细胞类型特异性必需基因,包括BCR和ABL1,以及在HL-60细胞中的IGF1R,其增殖依赖于胰岛素信号通路。