Cell perturbation screens for target identification by RNAi

8Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Over the last decade, cell-based screening has become a powerful method in target identification and plays an important role both in basic research and drug discovery. The availability of whole genome sequences and improvements in cell-based screening techniques opened new avenues for high-throughput experiments. Large libraries of RNA interference reagents available for many organisms allow the dissection of broad spectrum of cellular processes. Here, we describe the current state of the large-scale phenotype screening with a focus on cell-based screens. We underline the importance and provide details of screen design, scalability, performance, data analysis, and hit prioritization. Similar to classical high-throughput in vitro screens with defined-target approaches in the past, cell-based screens depend on a successful establishment of robust phenotypic assays, the ability to quantitatively measure phenotypic changes and bioinformatics methods for data analysis, integration, and interpretation. © 2012 Springer Science+Business Media New York.

Cite

CITATION STYLE

APA

Demir, K., & Boutros, M. (2012). Cell perturbation screens for target identification by RNAi. Methods in Molecular Biology, 910, 1–13. https://doi.org/10.1007/978-1-61779-965-5_1

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free