Single-cell microfluidic impedance cytometry: from raw signals to cell phenotypes using data analytics.
Single-cell microfluidic impedance cytometry: from raw signals to cell phenotypes using data analytics.
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DOI:
10.1039/d0lc00840k
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发表时间:
2021-01-05
期刊:
影响因子:
6.1
通讯作者:
Caselli F
中科院分区:
文献类型:
--
作者:
Honrado C;Bisegna P;Swami NS;Caselli F
The biophysical analysis of single-cells by microfluidic impedance cytometry is emerging as a label-free and high-throughput means to stratify the heterogeneity of cellular systems based on their electrophysiology. Emerging applications range from fundamental life-science and drug assessment research to point-of-care diagnostics and precision medicine. Recently, novel chip designs and data analytic strategies are laying the foundation for multiparametric cell characterization and subpopulation distinction, which are essential to understand biological function, follow disease progression and monitor cell behaviour in microsystems. In this tutorial review, we present a comparative survey of the approaches to elucidate cellular and subcellular features from impedance cytometry data, covering the related subjects of device design, data analytics (i.e., signal processing, dielectric modelling, population clustering), and phenotyping applications. We give special emphasis to the exciting recent developments of the technique (timeframe 2017–2020) and provide our perspective on future challenges and directions. Its synergistic application with microfluidic separation, sensor science and machine learning can form an essential toolkit for label-free quantification and isolation of subpopulations to stratify heterogeneous biosystems. Review of chip designs and data analytics to stratify heterogeneity in cellular systems via microfluidic impedance cytometry
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