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一种新型的 NGS 文库制备方法,用于描述碎片化 DNA 的天然末端。

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

机构信息

Claret Bioscience LLC, Santa Cruz, CA 95060, USA.

Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA 95064, USA.

出版信息

Nucleic Acids Res. 2020 May 7;48(8):e47. doi: 10.1093/nar/gkaa128.

Abstract

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.

摘要

生物和化学 DNA 片段化会生成具有各种末端的 DNA 分子,包括平末端和单链突出端。我们开发了一种下一代测序 (NGS) 检测方法 XACTLY,用于检测碎片化 DNA 的末端,这些信息在传统的 NGS 文库制备方法中通常会丢失。在这里,我们描述了 XACTLY 方法,展示了它的灵敏度和特异性,并证明了它在体外实验中的实用性。XACTLY 检测方法能够报告每个 DNA 片段上存在的所有长度和类型(5' 和 3')的单链突出端的相对丰度,如果存在的话,总体准确性在 80-90%之间。此外,XACTLY 在片段化后保留了每个天然 DNA 分子的序列,并能够以单核苷酸分辨率捕获切割事件的基因组景观。XACTLY 检测方法可作为一种新的研究和发现工具,用于碎片化分析和无细胞游离 DNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de02/7192605/f46be0495d3f/gkaa128fig1.jpg

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