Loss Minimized Data Reduction in Single-Cell Tomographic Phase Microscopy Using 3D Zernike Descriptors

Author:

Memmolo Pasquale1,Pirone Daniele12,Sirico Daniele Gaetano1,Miccio Lisa1,Bianco Vittorio1,Ayoub Ahmed Bassam3,Psaltis Demetri3,Ferraro Pietro1

Affiliation:

1. CNR-ISASI, Institute of Applied Sciences and Intelligent Systems “E. Caianiello”, Via Campi Flegrei 34, 80078 Pozzuoli, Napoli, Italy.

2. DIETI, Department of Electrical Engineering and Information Technologies, University of Naples “Federico II”, via Claudio 21, 80125 Napoli, Italy.

3. EPFL, Ecole Polytechnique Fédérale de Lausanne, Optics Laboratory, CH-1015 Lausanne, Switzerland.

Abstract

Tomographic phase microscopy (TPM) in flow cytometry is one of the most promising computational imaging techniques for the quantitative 3-dimensional (3D) analysis of unstained single cells. Continuous cells’ flow, combined with the stain-free mode, can assure the high-throughput collection of quantitative and informative 3D data. TPM promises to allow rapid cells’ screening by a nondestructive technique and with statistically relevant data. The current leading-edge research aimed at developing TPM systems in flow cytometry has already demonstrated the possibility of acquiring thousands of single-cell tomograms. Nevertheless, a key unsolved problem exists about the efficient storage and easy handling of such a huge amount of 3D data that prevents rapid analysis for cell diagnosis. Here, we show, for the first time, an effective encoding strategy of single-cell tomograms that can completely overcome this critical bottleneck. Essentially, by using the 3D version of Zernike polynomials, we demonstrate that the 3D refractive index distribution of a cell can be straightforwardly encoded in 1D with negligible information loss (<1%), thus greatly streamlining the data handling and storage. The performance analysis of the proposed method has been first assessed on simulated tomographic cell phantom, while the experimental validation has been extensively proofed on tomographic data from experiments with different cell lines. The results achieved here imply an intriguing breakthrough for TPM that promises to unlock computational pipelines for analyzing 3D data that were unattainable until now.

Publisher

American Association for the Advancement of Science (AAAS)

Reference55 articles.

1. High-Speed Imaging Meets Single-Cell Analysis

2. Review: Imaging technologies for flow cytometry;Han Y;Lab Chip,2016

3. Toward Deep Biophysical Cytometry: Prospects and Challenges

4. Perspectives on liquid biopsy for label-free detection of “circulating tumor cells” through intelligent lab-on-chips;Miccio L;Viewpoints,2020

5. High-speed fluorescence image–enabled cell sorting

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3