Digital PCR (dPCR) was first conceived for single-molecule quantitation. However, current dPCR systems often require DNA templates to share partitions due to limited partitioning capacities. Here, we introduce UltraPCR, a next-generation dPCR system where DNA counting is performed in a single-molecule regimen through a 6-log dynamic range using a swift and parallelized workflow. Each UltraPCR reaction is divided into >30 million partitions without microfluidics to achieve single template occupancy. Combined with a unique emulsion chemistry, partitions are optically clear, enabling the use of a three-dimensional imaging technique to rapidly detect DNA-positive partitions. Single-molecule occupancy also allows for more straightforward multiplex assay development due to the absence of partition-specific competition. As a proof of concept, we developed a 222-plex UltraPCR assay and demonstrated its potential use as a rapid, low-cost screening assay for noninvasive prenatal testing for as low as 4% trisomy fraction samples with high precision, accuracy, and reproducibility.
Next-Generation Digital Polymerase Chain Reaction: High-Dynamic-Range Single-Molecule DNA Counting via Ultrapartitioning.
下一代数字聚合酶链式反应:通过超分离实现高动态范围单分子DNA计数
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作者:Shum Eleen Y, Lai Janice H, Li Sixing, Lee Haeun G, Soliman Jesse, Raol Vedant K, Lee Cavina K, Fodor Stephen P A, Fan H Christina
| 期刊: | Analytical Chemistry | 影响因子: | 6.700 |
| 时间: | 2022 | 起止号: | 2022 Dec 27; 94(51):17868-17876 |
| doi: | 10.1021/acs.analchem.2c03649 | 研究方向: | 免疫/内分泌 |
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