Inter-laboratory automation of the in vitro micronucleus assay using imaging flow cytometry and deep learning

被引:0
|
作者
John W. Wills
Jatin R. Verma
Benjamin J. Rees
Danielle S. G. Harte
Qiellor Haxhiraj
Claire M. Barnes
Rachel Barnes
Matthew A. Rodrigues
Minh Doan
Andrew Filby
Rachel E. Hewitt
Catherine A. Thornton
James G. Cronin
Julia D. Kenny
Ruby Buckley
Anthony M. Lynch
Anne E. Carpenter
Huw D. Summers
George E. Johnson
Paul Rees
机构
[1] Swansea University,College of Engineering
[2] Cambridge University,Department of Veterinary Medicine
[3] Swansea University,Swansea University Medical School
[4] Luminex Corporation,Amnis Flow Cytometry
[5] GlaxoSmithKline,Bioimaging Analytics
[6] Newcastle University,Faculty of Medical Sciences
[7] GlaxoSmithKline Research and Development Platform,Imaging Platform
[8] Broad Institute of MIT and Harvard,undefined
来源
Archives of Toxicology | 2021年 / 95卷
关键词
Micronucleus test; Genetic toxicology; Compound screening; Machine learning; High throughput; Image analysis.;
D O I
暂无
中图分类号
学科分类号
摘要
The in vitro micronucleus assay is a globally significant method for DNA damage quantification used for regulatory compound safety testing in addition to inter-individual monitoring of environmental, lifestyle and occupational factors. However, it relies on time-consuming and user-subjective manual scoring. Here we show that imaging flow cytometry and deep learning image classification represents a capable platform for automated, inter-laboratory operation. Images were captured for the cytokinesis-block micronucleus (CBMN) assay across three laboratories using methyl methanesulphonate (1.25–5.0 μg/mL) and/or carbendazim (0.8–1.6 μg/mL) exposures to TK6 cells. Human-scored image sets were assembled and used to train and test the classification abilities of the “DeepFlow” neural network in both intra- and inter-laboratory contexts. Harnessing image diversity across laboratories yielded a network able to score unseen data from an entirely new laboratory without any user configuration. Image classification accuracies of 98%, 95%, 82% and 85% were achieved for ‘mononucleates’, ‘binucleates’, ‘mononucleates with MN’ and ‘binucleates with MN’, respectively. Successful classifications of ‘trinucleates’ (90%) and ‘tetranucleates’ (88%) in addition to ‘other or unscorable’ phenotypes (96%) were also achieved. Attempts to classify extremely rare, tri- and tetranucleated cells with micronuclei into their own categories were less successful (≤ 57%). Benchmark dose analyses of human or automatically scored micronucleus frequency data yielded quantitation of the same equipotent concentration regardless of scoring method. We conclude that this automated approach offers significant potential to broaden the practical utility of the CBMN method across industry, research and clinical domains. We share our strategy using openly-accessible frameworks.
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页码:3101 / 3115
页数:14
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