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10.1038/nmeth.4225

http://scihub22266oqcxt.onion/10.1038/nmeth.4225
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C5449203!5449203!28319113
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suck abstract from ncbi


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pmid28319113      Nat+Methods 2017 ; 14 (6): 573-6
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  • Combinatorial CRISPR-Cas9 screens for de novo mapping of genetic interactions #MMPMID28319113
  • Shen JP; Zhao D; Sasik R; Luebeck J; Birmingham A; Bojorquez-Gomez A; Licon K; Klepper K; Pekin D; Beckett A; Sanchez K; Thomas A; Kuo CC; Du D; Roguev A; Lewis NE; Chang AN; Kreisberg JF; Krogan N; Qi L; Ideker T; Mali P
  • Nat Methods 2017[Jun]; 14 (6): 573-6 PMID28319113show ga
  • We developed a systematic approach to map human genetic networks by combinatorial CRISPR-Cas9 perturbations coupled to robust analysis of growth kinetics. We targeted all pairs of 73 cancer genes with dual-guide RNAs in three cell lines, altogether comprising 141,912 tests of interaction. Numerous therapeutically relevant interactions were identified and these patterns replicated with combinatorial drugs at 75% precision. Based on these results we anticipate cellular context will be critical to synthetic-lethal therapies.
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