ArticleScientific reports2015
Φ-score: A cell-to-cell phenotypic scoring method for sensitive and selective hit discovery in cell-based assays.
Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Chromatin recruitment of OGG1 requires cohesin and mediator and is essential for efficient 8-oxoG removal.Nucleic acids research · 2020Article
- MasterPATH: network analysis of functional genomics screening data.BMC genomics · 2020Article
- Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields.Bioinformatics (Oxford, England) · 2017Article
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Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phenotypic screening monitors phenotypic changes induced by perturbations, including those generated by drugs or RNA interference. Currently-used methods for scoring screen hits have proven to be problematic, particularly when applied to physiologically relevant conditions such as low cell numbers or inefficient transfection. Here, we describe the Φ-score, which is a novel scoring method for the identification of phenotypic modifiers or hits in cell-based screens. Φ-score performance was assessed with simulations, a validation experiment and its application to gene identification in a large-scale RNAi screen. Using robust statistics and a variance model, we demonstrated that the Φ-score showed better sensitivity, selectivity and reproducibility compared to classical approaches. The improved performance of the Φ-score paves the way for cell-based screening of primary cells, which are often difficult to obtain from patients in sufficient numbers. We also describe a dedicated merging procedure to pool scores from small interfering RNAs targeting the same gene so as to provide improved visualization and hit selection.
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Registered trials
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