Single-Molecule Dna Sequencing Of Widely Varying Gc-Content Using Nucleotide Release, Capture And Detection In Microdroplets

Tim J Puchtler,Kerr Johnson,Rebecca N Palmer,Emma L Talbot,Lindsey A Ibbotson, Paulina K Powalowska, Rachel Knox,Aya Shibahara, Pedro M S Cunha, Oliver J Newell,Mei Wu, Jasmin Chana, Evangelia-Nefeli Athanasopoulou, Andreas M Waeber,Magdalena Stolarek,Ana-Luisa Silva, Justyna M Mordaka, Michael Haggis-Powell, Christina Xyrafaki,James Bush, Ibrahim S Topkaya,Maciej Sosna, Richard J Ingham,Thomas Huckvale,Aurel Negrea,Boris Breiner,Justinas Šlikas,Douglas J Kelly,Alexander J Dunning,Neil M Bell, Mark Dethlefsen,David M Love,Paul H Dear,Jekaterina Kuleshova, Gareth J Podd,Tom H Isaac,Barnaby W Balmforth,Cameron A Frayling

NUCLEIC ACIDS RESEARCH(2020)

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摘要
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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