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

Author:

Harkins Kelly M1ORCID,Schaefer Nathan K2,Troll Christopher J1,Rao Varsha1,Kapp Joshua3,Naughton Colin1,Shapiro Beth34ORCID,Green Richard E2

Affiliation:

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

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

3. Department of Ecology and Evolutionary Biology, University of California, Santa Cruz, CA 95064, USA

4. Howard Hughes Medical Institute, University of California, Santa Cruz, CA 95064, USA

Abstract

AbstractBiological 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.

Funder

Gordon and Betty Moore Foundation

NIH

Publisher

Oxford University Press (OUP)

Subject

Genetics

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