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Review
. 2018 Mar 11;19(3):807.
doi: 10.3390/ijms19030807.

Platforms for Single-Cell Collection and Analysis

Affiliations
Review

Platforms for Single-Cell Collection and Analysis

Lukas Valihrach et al. Int J Mol Sci. .

Abstract

Single-cell analysis has become an established method to study cell heterogeneity and for rare cell characterization. Despite the high cost and technical constraints, applications are increasing every year in all fields of biology. Following the trend, there is a tremendous development of tools for single-cell analysis, especially in the RNA sequencing field. Every improvement increases sensitivity and throughput. Collecting a large amount of data also stimulates the development of new approaches for bioinformatic analysis and interpretation. However, the essential requirement for any analysis is the collection of single cells of high quality. The single-cell isolation must be fast, effective, and gentle to maintain the native expression profiles. Classical methods for single-cell isolation are micromanipulation, microdissection, and fluorescence-activated cell sorting (FACS). In the last decade several new and highly efficient approaches have been developed, which not just supplement but may fully replace the traditional ones. These new techniques are based on microfluidic chips, droplets, micro-well plates, and automatic collection of cells using capillaries, magnets, an electric field, or a punching probe. In this review we summarize the current methods and developments in this field. We discuss the advantages of the different commercially available platforms and their applicability, and also provide remarks on future developments.

Keywords: analysis; collection; isolation; single cell.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Overview of currently used tools and principles for single-cell collection (adapted and modified from materials provided by the manufacturers and [74,82] with permission from Elsevier). FACS: fluorescence-activated cell sorting; LCM: laser capture microdissection.

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