Analysis of image-based phenotypic parameters for high throughput gene perturbation assays

被引:6
|
作者
Song, Mee [1 ]
Jeong, Euna [1 ]
Lee, Tae-Kyu [2 ]
Tsoy, Yury [3 ]
Kwon, Yong-Jun [2 ]
Yoon, Sukjoon [1 ,4 ]
机构
[1] Sookmyung Womens Univ, Ctr Adv Bioinformat & Syst Med, Seoul 140742, South Korea
[2] Inst Pasteur Korea, Discovery Biol Grp, Songnam 463400, Gyeonggi Do, South Korea
[3] Inst Pasteur Korea, Imaging Proc Platform, Songnam 463400, Gyeonggi Do, South Korea
[4] Sookmyung Womens Univ, Dept Biol Sci, Seoul 140742, South Korea
基金
新加坡国家研究基金会;
关键词
siRNA screening; Gene perturbation; Image-based assay; Phenotypic parameter; HUMAN-CELLS; RNAI; GENOME; MICROSCOPY; IDENTIFICATION; MIGRATION; SET;
D O I
10.1016/j.compbiolchem.2015.07.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although image-based phenotypic assays are considered a powerful tool for siRNA library screening, the reproducibility and biological implications of various image-based assays are not well-characterized in a systematic manner. Here, we compared the resolution of high throughput assays of image-based cell count and typical cell viability measures for cancer samples. It was found that the optimal plating density of cells was important to obtain maximal resolution in both types of assays. In general, cell counting provided better resolution than the cell viability measure in diverse batches of siRNAs. In addition to cell count, diverse image-based measures were simultaneously collected from a single screening and showed good reproducibility in repetitions. They were classified into a few functional categories according to biological process, based on the differential patterns of hit (i.e., siRNAs) prioritization from the same screening data. The presented systematic analyses of image-based parameters provide new insight to a multitude of applications and better biological interpretation of high content cell-based assays. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:192 / 198
页数:7
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