Sequencing by Expansion (SBX) - a novel, high-throughput single-molecule sequencing technology.

Mark Kokoris, Robert McRuer, Melud Nabavi, Aaron Jacobs, Marc Prindle, Cynthia Cech, Kendall Berg, Taylor Lehmann, Cara Machacek, John Tabone, Jagadeeswaran Chandrasekar, Lacey McGee, Matthew Lopez, Tommy Reid, Cara Williams, Salka Barrett, Alex Lehmann, Michael Kovarik, Robert Busam, Scott Miller, Brent Banasik, Brittany Kesic, Anasha Arryman, Megan Rogers-Peckham, Alan Kimura, Megan LeProwse, Mitchell Wolfin, Svetlana Kritzer, Joanne Leadbetter, Majid Babazedeh, John Chase, Greg Thiessen, William Lint, Drew Goodman, Dylan O'Connell, Nadya Lumanpauw, John Hoffman, Samantha Vellucci, Kendra Collins, Jessica Vellucci, Amy Taylor, Molly Murphy, Michael Lee, Matthew Corning
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Abstract

Remarkable advances in high-throughput sequencing have enabled major biological discoveries and clinical applications, but achieving wider distribution and use depends critically on further improvements in scale and cost reduction. Nanopore sequencing has long held the promise for such progress, but has had limited market penetration. This is because efficient and accurate nanopore sequencing of nucleic acids has been challenged by fundamental signal-to-noise limitations resulting from the poor spatial resolution and molecular distinction of nucleobases. Here, we describe Sequencing by Expansion (SBX), a single-molecule sequencing technology that overcomes these limitations by using a biochemical conversion process to encode the sequence of a target nucleic acid molecule into an Xpandomer, a highly measurable surrogate polymer. Expanding over 50 times longer than the parent DNA templates, Xpandomers are engineered with high signal-to-noise reporter codes to enable facile, high-accuracy nanopore sequencing. We demonstrate the performance of SBX and present the specialized molecular structures, chemistries, enzymes and methods that enable it. The innovative molecular and systems engineering in SBX create a transformative technology to address the needs of existing and emerging sequencing applications.

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扩增测序(SBX)是一种新型的高通量单分子测序技术。
高通量测序的显著进步使重大生物学发现和临床应用成为可能,但要实现更广泛的分布和使用,关键取决于规模的进一步改进和成本的降低。纳米孔测序长期以来一直有希望取得这样的进展,但市场渗透率有限。这是因为核酸的有效和准确的纳米孔测序受到了基本的信号噪声限制的挑战,这些限制是由核碱基的空间分辨率和分子区分差造成的。在这里,我们描述了扩增测序(SBX),这是一种单分子测序技术,它通过使用生化转化过程将目标核酸分子的序列编码成Xpandomer,一种高度可测量的替代聚合物,从而克服了这些限制。扩展超过母体DNA模板的50倍,xpandomer被设计成具有高信噪比报告代码,以实现方便,高精度的纳米孔测序。我们展示了SBX的性能,并介绍了使其成为可能的特殊分子结构、化学物质、酶和方法。SBX的创新分子和系统工程创造了一种变革性技术,以满足现有和新兴测序应用的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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