Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies

Cowley GS, Weir BA, Vazquez F, Tamayo P, Scott JA, Rusin S, East-Seletsky A, Ali LD, Gerath WF, Pantel SE, et al. Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies. Sci Data. 2014;1:140035.

NOTES

Cowley, Glenn SWeir, Barbara AVazquez, FranciscaTamayo, PabloScott, Justine ARusin, ScottEast-Seletsky, AlexandraAli, Levi DGerath, William FjPantel, Sarah ELizotte, Patrick HJiang, GuozhiHsiao, JessicaTsherniak, AviadDwinell, ElizabethAoyama, SimonOkamoto, MichaelHarrington, WilliamGelfand, EllenGreen, Thomas MTomko, Mark JGopal, ShubaWong, Terence CLi, HuboHowell, SaraStransky, NicolasLiefeld, TedJang, DongkeunBistline, JonathanHill Meyers, BarbaraArmstrong, Scott AAnderson, Ken CStegmaier, KimberlyReich, MichaelPellman, DavidBoehm, Jesse SMesirov, Jill PGolub, Todd RRoot, David EHahn, William CengT32 GM008704/GM/NIGMS NIH HHS/U01 CA176058/CA/NCI NIH HHS/U54 CA112962/CA/NCI NIH HHS/DatasetResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.EnglandSci Data. 2014 Sep 30;1:140035. doi: 10.1038/sdata.2014.35. eCollection 2014.

Abstract

Using a genome-scale, lentivirally delivered shRNA library, we performed massively parallel pooled shRNA screens in 216 cancer cell lines to identify genes that are required for cell proliferation and/or viability. Cell line dependencies on 11,000 genes were interrogated by 5 shRNAs per gene. The proliferation effect of each shRNA in each cell line was assessed by transducing a population of 11M cells with one shRNA-virus per cell and determining the relative enrichment or depletion of each of the 54,000 shRNAs after 16 population doublings using Next Generation Sequencing. All the cell lines were screened using standardized conditions to best assess differential genetic dependencies across cell lines. When combined with genomic characterization of these cell lines, this dataset facilitates the linkage of genetic dependencies with specific cellular contexts (e.g., gene mutations or cell lineage). To enable such comparisons, we developed and provided a bioinformatics tool to identify linear and nonlinear correlations between these features.
Last updated on 02/17/2021