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Updated: Jan 11, 2026

Ultra-long Read Sequencing for Whole Genomic DNA Analysis
Published on: March 15, 2019
Approaching single-molecule assembly-free readout from medium-length encoded DNA
Weigang Chen1,2,3, Rui Qin4, Quan Guo4
1School of Microelectronics, Tianjin University, Tianjin, China. chenwg@tju.edu.cn.
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.
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