Improving Detection of Rare Biological Events in High-Throughput Screens

Author:

Murie Carl12,Barette Caroline3,Button Jennifer1,Lafanechère Laurence34,Nadon Robert12

Affiliation:

1. McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada

2. Department of Human Genetics, McGill University, Montreal, Quebec, Canada

3. Equipe Criblage pour des Molécules Bio-Actives (CMBA), U1038 INSERM/CEA/UJF, CEA Grenoble, Grenoble Cedex 09, France

4. Institut Albert Bonniot, CRI INSERM/UJF U823, Team 3 “Polarity, Development and Cancer,” Rond-point de la Chantourne, La Tronche Cedex, France

Abstract

The success of high-throughput screening (HTS) strategies depends on the effectiveness of both normalization methods and study design. We report comparisons among normalization methods in two titration series experiments. We also extend the results in a third experiment with two differently designed but otherwise identical screens: compounds in replicate plates were either placed in the same well locations or were randomly assigned to different locations. Best results were obtained when randomization was combined with normalization methods that corrected for within-plate spatial bias. We conclude that potent, reliable, and accurate HTS requires replication, randomization design strategies, and more extensive normalization than is typically done and that formal statistical testing is desirable. The Statistics and dIagnostic Graphs for HTS (SIGHTS) Microsoft Excel Add-In software is available to conduct most analyses reported here.

Publisher

Elsevier BV

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