DNAcycP2: improved estimation of intrinsic DNA cyclizability through data augmentation
Loop-seq is a pioneering high-throughput assay that enables the simultaneous quantification of intrinsic cyclizability across a large set of DNA fragments. However, the assay's reliance on biotin-tethered elongated DNA fragments introduces a tethering effect, leading to biased cyclizability measurements. We demonstrate that the current de-biasing technique is inadequate for fully mitigating this bias. To address this, we introduce DNAcycP2, an enhanced software tool that extends the capabilities of our previous platform, DNAcycP. DNAcycP2 incorporates a novel data augmentation approach to more effectively eliminate biotin tether bias, yielding more accurate estimates of intrinsic DNA cyclizability. Additionally, DNAcycP2 offers improved computational efficiency and expands accessibility through a newly developed R package alongside its existing Python package and web server, ensuring broader utility for the research community.
Authors
- Xiaozhong Wang (ORCID: https://orcid.org/0000-0003-0219-0752)
- Ji-Ping Wang (ORCID: https://orcid.org/0000-0002-8398-939X)
- Chong Jin (ORCID: https://orcid.org/0000-0003-4863-3328)
- Keren Li (ORCID: https://orcid.org/0000-0001-6253-9747)
- Feng Ruan (ORCID: https://orcid.org/0000-0003-1336-8229)
- Brody Kendall
Institutions
- Northwestern University (US)
- New Jersey Institute of Technology (US)
- University of Alabama at Birmingham (US)
Publication Details
- Journal
- Nucleic Acids Research
- Published
- 2025-02-27
- DOI
- https://doi.org/10.1093/nar/gkaf145
- Citations
- 4
- Primary Topic
- Genomics and Chromatin Dynamics
- Type
- article
- Field-Weighted Citation Impact
- 3.22