Approaching single-molecule assembly-free readout from medium-length encoded DNA.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41249129.
- Also identified by DOI 10.1038/s41467-025-65004-7 and PMC identifier 12623992.
- Licence recorded as CC BY-NC-ND.
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Abstract
For DNA data storage, nanopore sequencing can facilitate rapid readout but suffers from severe insertion/deletion errors, which are quite computationally expensive to correct. Here, we propose a nearly single-molecule and assembly-free readout scheme for medium-length pseudo-noise piloting DNA fragments. Specifically, we devise medium-length DNA fragments using low-density parity-check codes companioned by pseudo-noise sequence (PNC-LDPC). A single cleavage on this encoded DNA by transposase generates DNA fragments of approximately full length. Using the readout-aware pseudo-noise sequences, noisy nanopore reads with arbitrary start points are directly located, and base insertions/deletions are corrected, enabling fast and reliable recovery even at very low coverages. Experimental results indicate that the data can be reliably recovered at a coverage of 1.24-3.15× with a typical nanopore sequencing error rate of 1.83%. This method enables error-free recovery in near single-molecule scenarios, highlighting the potential of PNC-LDPC encoded medium-length DNA for data storage applications.
Medical subject headings
- DNA
- Nanopore Sequencing
- Sequence Analysis, DNA