Data Standardization for Results Management.
Campbell RM, Dymshitz J, Eastwood BJ, Emkey R, Greenen DP, Heerding JM, Johnson D, Large TH, Littlejohn T, Montrose C, Nutter SE, Sawyer BD, Sigmund SK, Smith M, Weidner JR, Zink RW.
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2012 May 1 [updated 2017 Oct 20]. In: Markossian S, Grossman A, Baskir H, Arkin M, Auld D, Austin C, Baell J, Brimacombe K, Chung TDY, Coussens NP, Dahlin JL, Devanarayan V, Foley TL, Glicksman M, Gorshkov K, Grotegut S, Hall MD, Hoare S, Inglese J, Iversen PW, Lal-Nag M, Li Z, Manro JR, McGee J, Norvil A, Pearson M, Riss T, Saradjian P, Sittampalam GS, Tarselli MA, Trask OJ Jr, Weidner JR, Wildey MJ, Wilson K, Xia M, Xu X, editors. Assay Guidance Manual [Internet]. Bethesda (MD): Eli Lilly & Company and the National Center for Advancing Translational Sciences; 2004–.
PMID: 22553865
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Raw data collected in screening assays should be appropriately analyzed to derive activity expressed as potency or efficacy values of tested compounds (IC(50) or EC(50) values). In this chapter the authors discuss standardized approaches to processing radioligand binding, …
Raw data collected in screening assays should be appropriately analyzed to derive activity expressed as potency or efficacy values of tested …