Machine learning approach for discrimination of genotypes based on bright-field cellular images

被引:0
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作者
Godai Suzuki
Yutaka Saito
Motoaki Seki
Daniel Evans-Yamamoto
Mikiko Negishi
Kentaro Kakoi
Hiroki Kawai
Christian R. Landry
Nozomu Yachie
Toutai Mitsuyama
机构
[1] National Institute of Advanced Industrial Science and Technology (AIST),Artificial Intelligence Research Center
[2] AIST-Waseda University Computational Bio Big-Data Open Innovation Laboratory (CBBD-OIL),Graduate School of Frontier Sciences
[3] The University of Tokyo,Research Center for Advanced Science and Technology
[4] The University of Tokyo,Institute for Advanced Biosciences
[5] Keio University,Systems Biology Program, Graduate School of Media and Governance
[6] Keio University,Research and Development Department
[7] LPIXEL Inc.,Institut de Biologie Intégrative et des Systémes
[8] Université Laval,Département de Biochimie, Microbiologie et Bio
[9] Université Laval,informatique, Faculté de sciences et génie
[10] Université Laval,PROTEO, le regroupement québécois de recherche sur la fonction, l’ingénierie et les applications des protéines
[11] Université Laval,Centre de Recherche en Données Massives (CRDM)
[12] Université Laval,Département de Biologie, Faculté des sciences et de Génie
[13] The University of British Columbia,School of Biomedical Engineering
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摘要
Morphological profiling is a combination of established optical microscopes and cutting-edge machine vision technologies, which stacks up successful applications in high-throughput phenotyping. One major question is how much information can be extracted from an image to identify genetic differences between cells. While fluorescent microscopy images of specific organelles have been broadly used for single-cell profiling, the potential ability of bright-field (BF) microscopy images of label-free cells remains to be tested. Here, we examine whether single-gene perturbation can be discriminated based on BF images of label-free cells using a machine learning approach. We acquired hundreds of BF images of single-gene mutant cells, quantified single-cell profiles consisting of texture features of cellular regions, and constructed a machine learning model to discriminate mutant cells from wild-type cells. Interestingly, the mutants were successfully discriminated from the wild type (area under the receiver operating characteristic curve = 0.773). The features that contributed to the discrimination were identified, and they included those related to the morphology of structures that appeared within cellular regions. Furthermore, functionally close gene pairs showed similar feature profiles of the mutant cells. Our study reveals that single-gene mutant cells can be discriminated from wild-type cells based on BF images, suggesting the potential as a useful tool for mutant cell profiling.
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