An integrated one-step system to extract, analyze and annotate all relevant information from image-based cell screening of chemical libraries

被引:12
作者
Rabal, Obdulia [1 ]
Link, Wolfgang [1 ]
Serelde, Beatriz G. [1 ]
Bischoff, James R. [1 ]
Oyarzabal, Julen [1 ]
机构
[1] Spanish Natl Canc Res Ctr CNIO, Expt Therapeut Programme, Madrid 28029, Spain
关键词
DRUG DISCOVERY; INHIBITORS; CLASSIFICATION; IDENTIFICATION; SELECTION; PTEN;
D O I
10.1039/b919830j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here we report the development and validation of a complete solution to manage and analyze the data produced by image-based phenotypic screening campaigns of small-molecule libraries. In one step initial crude images are analyzed for multiple cytological features, statistical analysis is performed and molecules that produce the desired phenotypic pro. le are identified. A naive Bayes classifier, integrating chemical and phenotypic spaces, is built and utilized during the process to assess those images initially classified as "fuzzy''-an automated iterative feedback tuning. Simultaneously, all this information is directly annotated in a relational database containing the chemical data. This novel fully automated method was validated by conducting a re-analysis of results from a high-content screening campaign involving 33 992 molecules used to identify inhibitors of the PI3K/Akt signaling pathway. Ninety-two percent of confirmed hits identified by the conventional multistep analysis method were identified using this integrated one-step system as well as 40 new hits, 14.9% of the total, originally false negatives. Ninety-six percent of true negatives were properly recognized too. A web-based access to the database, with customizable data retrieval and visualization tools, facilitates the posterior analysis of annotated cytological features which allows identi. cation of additional phenotypic profiles; thus, further analysis of original crude images is not required.
引用
收藏
页码:711 / 720
页数:10
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