论文标题

基于机器学习的无镜头成像技术,用于现场 - 可容纳的细胞仪

Machine learning based lens-free imaging technique for field-portable cytometry

论文作者

Vaghashiya, Rajkumar, Shin, Sanghoon, Chauhan, Varun, Kapadiya, Kaushal, Sanghavi, Smit, Seo, Sungkyu, Roy, Mohendra

论文摘要

无镜头的阴影成像技术(LSIT)是一种表征微粒和生物细胞的良好技术。 Due to its simplicity and cost-effectiveness, various low-cost solutions have been evolved, such as automatic analysis of complete blood count (CBC), cell viability, 2D cell morphology, 3D cell tomography, etc. The developed auto characterization algorithm so far for this custom-developed LSIT cytometer was based on the hand-crafted features of the cell diffraction patterns from the LSIT cytometer, that were determined from our关于成千上万个单个细胞类型样本的经验发现,这些样本限制了系统的自动分类或表征的新细胞类型。此外,由于其信号较小或背景噪声,其性能遭受了不良图像(细胞衍射模式)标志的困扰。在这项工作中,我们通过利用人工智能驱动的自动信号增强方案来解决这些问题,例如基于深层神经网络中学习的传递,诸如DENOO AUTOCONEDER和自适应细胞表征技术。我们提出的方法的性能显示,对于大多数细胞类型,例如红细胞(RBC)和白细胞(WBC),精度> 98%> 98%,以及信号增强> 5 dB。此外,该模型可以自适应地学习一些学习迭代中的新样本,并能够成功对新引入的样本和现有其他样本类型进行分类。

Lens-free Shadow Imaging Technique (LSIT) is a well-established technique for the characterization of microparticles and biological cells. Due to its simplicity and cost-effectiveness, various low-cost solutions have been evolved, such as automatic analysis of complete blood count (CBC), cell viability, 2D cell morphology, 3D cell tomography, etc. The developed auto characterization algorithm so far for this custom-developed LSIT cytometer was based on the hand-crafted features of the cell diffraction patterns from the LSIT cytometer, that were determined from our empirical findings on thousands of samples of individual cell types, which limit the system in terms of induction of a new cell type for auto classification or characterization. Further, its performance is suffering from poor image (cell diffraction pattern) signatures due to its small signal or background noise. In this work, we address these issues by leveraging the artificial intelligence-powered auto signal enhancing scheme such as denoising autoencoder and adaptive cell characterization technique based on the transfer of learning in deep neural networks. The performance of our proposed method shows an increase in accuracy >98% along with the signal enhancement of >5 dB for most of the cell types, such as Red Blood Cell (RBC) and White Blood Cell (WBC). Furthermore, the model is adaptive to learn new type of samples within a few learning iterations and able to successfully classify the newly introduced sample along with the existing other sample types.

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