Abstract
Despite remarkable progress in DNA sequencing technologies there remains a trade-off between short-read platforms, having limited ability to sequence homopolymers, repeated motifs or long-range structural variation, and long-read platforms, which tend to have lower accuracy and/or throughput. Moreover, current methods do not allow direct readout of epigenetic modifications from a single read. With the aim of addressing these limitations, we have developed an optical electrowetting sequencing platform that uses step-wise nucleotide triphosphate (dNTP) release, capture and detection in microdroplets from single DNA molecules. Each microdroplet serves as a reaction vessel that identifies an individual dNTP based on a robust fluorescence signal, with the detection chemistry extended to enable detection of 5-methylcytosine. Our platform uses small reagent volumes and inexpensive equipment, paving the way to cost-effective single-molecule DNA sequencing, capable of handling widely varying GC-bias, and demonstrating direct detection of epigenetic modifications.
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CITATION STYLE
Puchtler, T. J., Johnson, K., Palmer, R. N., Talbot, E. L., Ibbotson, L. A., Powalowska, P. K., … Frayling, C. A. (2020). Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets. Nucleic Acids Research, 48(22), E132. https://doi.org/10.1093/nar/gkaa987
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