Digital microfluidics-based digital counting of single-cell copy number variation (dd-scCNV Seq)

Abstract

Single-cell copy number variations (CNVs), major dynamic changes in humans, result in differential levels of gene expression and account for adaptive traits or underlying disease. Single-cell sequencing is needed to reveal these CNVs but has been hindered by single-cell whole-genome amplification (scWGA) bias, leading to inaccurate gene copy number counting. In addition, most of the current scWGA methods are labor intensive, time-consuming, and expensive with limited wide application. Here, we report a unique single-cell whole-genome library preparation approach based on d igital microfluidics for d igital counting of s ingle- c ell C opy N umber V ariation (dd-scCNV Seq). dd-scCNV Seq directly fragments the original single-cell DNA and uses these fragments as templates for amplification. These reduplicative fragments can be filtered computationally to generate the original partitioned unique identified fragments, thereby enabling digital counting of copy number variation. dd-scCNV Seq showed an increase in uniformity in the single-molecule data, leading to more accurate CNV patterns compared to other methods with low-depth sequencing. Benefiting from digital microfluidics, dd-scCNV Seq allows automated liquid handling, precise single-cell isolation, and high-efficiency and low-cost genome library preparation. dd-scCNV Seq will accelerate biological discovery by enabling accurate profiling of copy number variations at single-cell resolution.

Integrating microfluidics and synthetic biology: advancements and diverse applications across organisms

“…DMF is particularly useful for integrating genomic analysis. 50,129,130 An example is Lamanna et al , 111 created a pipeline called DISCO for isolating single cells and collecting the cell contents for either genome, transcriptome, or proteome analyses. The workflow on the DISCO consists of the cells being co-cultured and put through certain conditions for selection experiments.…”

Integrated Microwell Array-Based Microfluidic Chip with a Hand-Held Smartphone-Controlled Device for Nucleic Acid Detection

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