Abstract

Frequently, neural network training involving biological images suffers from a lack of data, resulting in inefficient network learning. This issue stems from limitations in terms of time, resources, and difficulty in cellular experimentation and data collection. For example, when performing experimental analysis, it may be necessary for the researcher to use most of their data for testing, as opposed to model training. Therefore, the goal of this paper is to perform dataset augmentation using generative adversarial networks (GAN) to increase the classification accuracy of deep convolutional neural networks (CNN) trained on induced pluripotent stem cell microscopy images. The main challenges are: 1. modeling complex data using GAN and 2. training neural networks on augmented datasets that contain generated data. To address these challenges, a temporally constrained, hierarchical classification scheme that exploits domain knowledge is employed for model learning. First, image patches of cell colonies from gray-scale microscopy images are generated using GAN, and then these images are added to the real dataset and used to address class imbalances at multiple stages of training. Overall, a 2% increase in both true positive rate and F1-score is observed using this method as compared to a straightforward, imbalanced classification network, with some greater improvements on a classwise basis. This work demonstrates that synergistic model design involving domain knowledge is key for biological image analysis and improves model learning in high-throughput scenarios.

Highlights

  • IntroductionStem cells are unspecialized cells that are used as a model for early-stage growth

  • Stem cells are unspecialized cells that are used as a model for early-stage growth.They recapitulate biological characteristics of embryonic development, most importantly pluripotency, or the lack of specified cellular purpose [1]

  • Data for this study come from experiments performed by Dr Barbara Davis in the laboratory of Dr Prue Talbot. They are aimed at determining the effects of nicotine exposure on diseased, induced pluripotent stem cells expressing the Huntington’s disease (HD) phenotype

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Summary

Introduction

Stem cells are unspecialized cells that are used as a model for early-stage growth They recapitulate biological characteristics of embryonic development, most importantly pluripotency, or the lack of specified cellular purpose [1]. Deviations from this pluripotent state are an indication of differentiation, or phenotypic lineage commitment, and have implications on the health and developmental status of cells and cellular colonies [2]. Adult cells have been turned back into stem cells in vitro (induced pluripotent stem cells, iPSC’s), and normal stem cell differentiation has been modeled using Markovian stochastic methods [6,7,8]

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