High-Throughput, Liquid-Based Genome-Wide RNAi Screening in C. elegans

Author(s):  
Linda P. O’Reilly ◽  
Ryan R. Knoerdel ◽  
Gary A. Silverman ◽  
Stephen C. Pak
2012 ◽  
Vol 29 (4) ◽  
pp. 459-470 ◽  
Author(s):  
Kaylene J. Simpson ◽  
Gregory M. Davis ◽  
Peter R. Boag

Author(s):  
Barbara Squiban ◽  
Jérôme Belougne ◽  
Jonathan Ewbank ◽  
Olivier Zugasti

2014 ◽  
Vol 20 (8) ◽  
pp. 998-1002 ◽  
Author(s):  
Rui Zhong ◽  
Xiaonan Dong ◽  
Beth Levine ◽  
Yang Xie ◽  
Guanghua Xiao

High-throughput RNA interference (RNAi) screening has opened up a path to investigating functional genomics in a genome-wide pattern. However, such studies are often restricted to assays that have a single readout format. Recently, advanced image technologies have been coupled with high-throughput RNAi screening to develop high-content screening, in which one or more cell image(s), instead of a single readout, were generated from each well. This image-based high-content screening technology has led to genome-wide functional annotation in a wider spectrum of biological research studies, as well as in drug and target discovery, so that complex cellular phenotypes can be measured in a multiparametric format. Despite these advances, data analysis and visualization tools are still largely lacking for these types of experiments. Therefore, we developed iScreen (image-Based High-content RNAi Screening Analysis Tool), an R package for the statistical modeling and visualization of image-based high-content RNAi screening. Two case studies were used to demonstrate the capability and efficiency of the iScreen package. iScreen is available for download on CRAN ( http://cran.cnr.berkeley.edu/web/packages/iScreen/index.html ). The user manual is also available as a supplementary document.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Sarah E. Pierce ◽  
Jeffrey M. Granja ◽  
William J. Greenleaf

AbstractChromatin accessibility profiling can identify putative regulatory regions genome wide; however, pooled single-cell methods for assessing the effects of regulatory perturbations on accessibility are limited. Here, we report a modified droplet-based single-cell ATAC-seq protocol for perturbing and evaluating dynamic single-cell epigenetic states. This method (Spear-ATAC) enables simultaneous read-out of chromatin accessibility profiles and integrated sgRNA spacer sequences from thousands of individual cells at once. Spear-ATAC profiling of 104,592 cells representing 414 sgRNA knock-down populations reveals the temporal dynamics of epigenetic responses to regulatory perturbations in cancer cells and the associations between transcription factor binding profiles.


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