Evidence map›Paper›PMID 26382112›Full record

ArticleScientific reports2015

Φ-score: A cell-to-cell phenotypic scoring method for sensitive and selective hit discovery in cell-based assays.

Laurent Guyon, Christian Lajaunie, Frédéric Fer, Ricky Bhajun, Eric Sulpice, Guillaume Pinna, Anna Campalans, J Pablo Radicella, Philippe Rouillier, Mélissa Mary and 4 more

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Laurent GuyonUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Christian LajaunieMINES ParisTech, PSL-Research University, CBIO-Centre for Computational Biology, F-77300 Fontainebleau, France.
Frédéric FerUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Ricky BhajunUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Eric SulpiceUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Guillaume PinnaPlateforme ARN interférence (PArI), DSV/IBITEC-S/SBIGEM/UMR 9198, CEA SACLAY, F-91191 Gif-sur-Yvette.
Anna CampalansCEA, Institute of Molecular and Cellular Radiobiology, F-92265 Fontenay aux Roses, France.
J Pablo RadicellaCEA, Institute of Molecular and Cellular Radiobiology, F-92265 Fontenay aux Roses, France.
Philippe RouillierMINES ParisTech, PSL-Research University, CBIO-Centre for Computational Biology, F-77300 Fontainebleau, France.
Mélissa MaryUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Stéphanie CombeUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Patricia ObeidUniversité Grenoble-Alpes, F-38000 Grenoble, France.
Jean-Philippe VertMINES ParisTech, PSL-Research University, CBIO-Centre for Computational Biology, F-77300 Fontainebleau, France.
Xavier GidrolUniversité Grenoble-Alpes, F-38000 Grenoble, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Identifiers

PMID26382112
PMCPMC4585642

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.