A Multivariate Computational Method to Analyze High-Content RNAi Screening Data. (September 2015)

• Record Type: Journal Article
• Authors: Rameseder, Jonathan; Krismer, Konstantin; Dayma, Yogesh; Ehrenberger, Tobias; Hwang, Mun Kyung; Airoldi, Edoardo M.; Floyd, Scott R.; Yaffe, Michael B.
• Other Names: Bickle Marc guest-editor.; Djaballah Hakim guest-editor.; Mayr Lorenz Martin guest-editor.
• Is Part Of: Journal of biomolecular screening. Volume 20:Number 8(2015)
• Page Start: 985
• Page End: 997
• Publication Date: 2015-09
• Subjects: high-content screening -- RNAi screening -- multivariate data analysis -- feature selection -- hit identification; Drugs -- Analysis -- Periodicals; Drugs -- Testing -- Periodicals; Biomolecules -- Analysis -- Periodicals; 572.36
• DOI: 10.1177/1087057115583037
• Languages: English
• ISSNs: 1087-0571

Abstract

High-content screening (HCS) using RNA interference (RNAi) in combination with automated microscopy is a powerful investigative tool to explore complex biological processes. However, despite the plethora of data generated from these screens, little progress has been made in analyzing HC data using multivariate methods that exploit the full richness of multidimensional data. We developed a novel multivariate method for HCS, multivariate robust analysis method (M-RAM), integrating image feature selection with ranking of perturbations for hit identification, and applied this method to an HC RNAi screen to discover novel components of the DNA damage response in an osteosarcoma cell line. M-RAM automatically selects the most informative phenotypic readouts and time points to facilitate the more efficient design of follow-up experiments and enhance biological understanding. Our method outperforms univariate hit identification and identifies relevant genes that these approaches would have missed. We found that statistical cell-to-cell variation in phenotypic responses is an important predictor of hits in RNAi-directed image-based screens. Genes that we identified as modulators of DNA damage signaling in U2OS cells include B-Raf, a cancer driver gene in multiple tumor types, whose role in DNA damage signaling we confirm experimentally, and multiple subunits of protein kinase A.