| Literature DB >> 29652558 |
Mridu Sinha1,2,3, Hannah Mack1,2,3, Todd P Coleman1,3, Stephanie I Fraley1,2,3.
Abstract
DNA melting analysis provides a rapid method for genotyping a target amplicon directly after PCR amplification. To transform melt genotyping into a broad-based profiling approach for heterogeneous samples, we previously proposed the integration of universal PCR and melt analysis with digital PCR. Here, we advanced this concept by developing a high-resolution digital melt platform with precise thermal control to accomplish reliable, high-throughput heat ramping of microfluidic chip digital PCR reactions. Using synthetic DNA oligos with defined melting temperatures, we characterized sources of melting variability and minimized run-to-run variations. Within-run comparisons throughout a 20,000-reaction chip revealed that high-melting-temperature sequences were significantly less prone to melt variation. Further optimization using bacterial 16S amplicons revealed a strong dependence of the number of melting transitions on the heating rate during curve generation. These studies show that reliable high-resolution melt curve genotyping can be achieved in digital, picoliter-scale reactions and demonstrate that rate-dependent melt signatures may be useful for enhancing automated melt genotyping.Entities:
Keywords: automated biology; engineering; high-throughput chemistry; informatics and software; point-of-care testing (POCT)
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Year: 2018 PMID: 29652558 DOI: 10.1177/2472630318769846
Source DB: PubMed Journal: SLAS Technol ISSN: 2472-6303 Impact factor: 3.047