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A novel NGS library preparation method to characterize native termini of fragmented DNA

机译:一种新型的NGS文库制备方法,表征分段DNA天然末端

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摘要

Biological and chemical DNA fragmentation generates DNA molecules with a variety of termini, including blunt ends and single-stranded overhangs. We have developed a Next Generation Sequencing (NGS) assay, XACTLY, to interrogate the termini of fragmented DNA, information traditionally lost in standard NGS library preparation methods. Here we describe the XACTLY method, showcase its sensitivity and specificity, and demonstrate its utility in in vitro experiments. The XACTLY assay is able to report relative abundances of all lengths and types (5' and 3') of single-stranded overhangs, if present, on each DNA fragment with an overall accuracy between 80-90%. In addition, XACTLY retains the sequence of each native DNA molecule after fragmentation and can capture the genomic landscape of cleavage events at single nucleotide resolution. The XACTLY assay can be applied as a novel research and discovery tool for fragmentation analyses and in cell-free DNA.
机译:生物和化学DNA碎片产生具有多种末端的DNA分子,包括钝端和单链悬垂。 我们已经开发了下一代测序(NGS)测定,XANTLY,以询问分段DNA的末端,传统上在标准NGS文库制备方法中丢失的信息。 在这里,我们描述了XACT方法,展示其敏感性和特异性,并证明其在体外实验中的实用性。 XANTSICSICESSICASE能够在每个DNA片段上报告单链悬垂的所有长度和类型(5'和3')的相对丰度,其DNA片段在80-90%之间的整体精度之间。 另外,XACT地保留在碎片后的每个天然DNA分子的序列,并且可以以单核苷酸分辨率捕获切割事件的基因组景观。 XANTICLY测定可作为碎片分析和无细胞DNA的新型研究和发现工具应用。

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