DeLHCA: Deep transfer learning for high-content analysis of the effects of drugs on immune cells

被引:0
作者
Hussain, Shaista [1 ]
Das, Ankit [1 ]
Nguyen, Binh P. [2 ]
Marzuki, Mardiana [4 ]
Lin, Shuping [5 ]
Kumar, Arun [3 ]
Wright, Graham [5 ]
Singhal, Amit [4 ]
机构
[1] Inst High Performance Comp, Singapore, Singapore
[2] VUW, Sch Math & Stat, Wellington, New Zealand
[3] NITR, Dept CS, Rourkela, India
[4] Singapore Immunol Network, Singapore, Singapore
[5] Skin Res Inst Singapore, Singapore, Singapore
来源
PROCEEDINGS OF THE 2019 IEEE REGION 10 CONFERENCE (TENCON 2019): TECHNOLOGY, KNOWLEDGE, AND SOCIETY | 2019年
关键词
High-Content Imaging; Drug Discovery; Unsupervised Machine Learning; Convolutional Neural Networks;
D O I
10.1109/tencon.2019.8929476
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Analysis of high-content screening (HCS) data mostly relies on supervised machine learning based approaches employing user-defined image features. This strategy has limited applications due to the requirement of a priori knowledge of expected cellular phenotypes / perturbations and the time-consuming process of manually annotating these phenotypes. To address these issues, we propose a machine learning based unsupervised framework for high-content analysis. The framework performs anomaly detection using features transferred from natural images to the cellular images by deep learning models. We applied this framework to detect anomalous effects of FDA approved drugs on human monocytic cells. Drug anomaly detection based on image features derived using three deep learning architectures, DenseNet-121, ResNet-50 and VGG-16, is compared with the anomaly scores computed from user-defined features extracted from individually segmented cells. The drug anomaly scores of automatically extracted deep features and user-defined features were found to be comparable. Our method has broad implications for faster and reliable analysis of high-content data with limited human interaction which can provide new biological insights and identification of drug candidates for repurposing of FDA approved drugs for new clinical conditions.
引用
收藏
页码:796 / 801
页数:6
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