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Median absolute deviation to improve hit selection for genome-scale RNAi screens
Chung N.1; Zhang X.D.1; Kreamer A.1; Locco L.1; Kuan P.-F.1; Bartz S.2; Linsley P.S.2; Ferrer M.1; Strulovici B.1
2008-03-01
Source PublicationJournal of Biomolecular Screening
ISSN10870571 1552454X
Volume13Issue:2Pages:149-158
AbstractHigh-throughput screening (HTS) of large-scale RNA interference (RNAi) libraries has become an increasingly popular method of functional genomics in recent years. Cell-based assays used for RNAi screening often produce small dynamic ranges and significant variability because of the combination of cellular heterogeneity, transfection efficiency, and the intrinsic nature of the genes being targeted. These properties make reliable hit selection in the RNAi screen a difficult task. The use of robust methods based on median and median absolute deviation (MAD) has been suggested to improve hit selection in such cases, but mean and standard deviation (SD)-based methods are still predominantly used in many RNAi HTS. In an experimental approach to compare these 2 methods, a genome-scale small interfering RNA (siRNA) screen was performed, in which the identification of novel targets increasing the therapeutic index of the chemotherapeutic agent mitomycin C (MMC) was sought. MAD values were resistant to the presence of outliers, and the hits selected by the MAD-based method included all the hits that would be selected by SD-based method as well as a significant number of additional hits. When retested in triplicate, a similar percentage of these siRNAs were shown to genuinely sensitize cells to MMC compared with the hits shared between SD- and MAD-based methods. Confirmed hits were enriched with the genes involved in the DNA damage response and cell cycle regulation, validating the overall hit selection strategy. Finally, computer simulations showed the superiority and generality of the MAD-based method in various RNAi HTS data models. In conclusion, the authors demonstrate that the MAD-based hit selection method rescued physiologically relevant false negatives that would have been missed in the SD-based method, and they believe it to be the desirable 1st-choice hit selection method for RNAi screen results. © 2008 Society for Biomolecular Sciences.
KeywordData analysis Functional genomics High-throughput screen Hit selection MAD Median absolute deviation RNA interference RNAi siRNA
DOI10.1177/1087057107312035
URLView the original
Language英語
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Cited Times [WOS]:106   [WOS Record]     [Related Records in WOS]
Document TypeJournal article
CollectionFaculty of Health Sciences
Affiliation1.Merck Research Laboratories
2.Rosetta Inpharmatics LLC
3.University of Wisconsin Madison
4.Bristol-Myers Squibb
Recommended Citation
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Chung N.,Zhang X.D.,Kreamer A.,et al. Median absolute deviation to improve hit selection for genome-scale RNAi screens[J]. Journal of Biomolecular Screening,2008,13(2):149-158.
APA Chung N..,Zhang X.D..,Kreamer A..,Locco L..,Kuan P.-F..,...&Strulovici B..(2008).Median absolute deviation to improve hit selection for genome-scale RNAi screens.Journal of Biomolecular Screening,13(2),149-158.
MLA Chung N.,et al."Median absolute deviation to improve hit selection for genome-scale RNAi screens".Journal of Biomolecular Screening 13.2(2008):149-158.
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