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Updated: Nov 8, 2025

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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Cooperative sequence clustering and decoding for DNA storage system with fountain codes.

Jaeho Jeong1, Seong-Joon Park1, Jae-Won Kim2

  • 1Department of Electrical and Computer Engineering, Seoul National University, Institute of New Media and Communications (INMC), Seoul 08826, South Korea.

Bioinformatics (Oxford, England)
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Summary

This study enhances DNA data storage by improving decoding performance. New methods utilize more sequence reads, reducing data retrieval costs without increasing writing expenses.

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Area of Science:

  • Biotechnology
  • Bioinformatics
  • Data Storage

Background:

  • DNA data storage systems face a trade-off between writing and reading costs.
  • Higher code rates save writing costs but increase sequencing reads for retrieval.
  • Current research treats clustering, alignment, and decoding as separate stages.

Purpose of the Study:

  • To improve DNA data storage by reducing reading costs without increasing writing costs.
  • To develop a unified decoding process integrating information from clustering, alignment, and decoding.
  • To validate experimental DNA synthesis and sequencing for practical error assessment.

Main Methods:

  • Developed a decoding process integrating Hamming-distance clustering, abnormal read discarding, Reed-Solomon error correction, and quality score-based ordering.
  • Synthesized 513.6 KB of data into DNA oligo pools.
  • Sequenced synthesized DNA using an Illumina MiSeq instrument.

Main Results:

  • Successfully synthesized and sequenced 513.6 KB of data.
  • The proposed decoding method incorporated previously discarded reads with minor errors.
  • Utilized 10.6-11.9% more sequence reads, reducing reading costs by 6.5-8.9% compared to prior research.
  • Provided channel characteristics including sequence coverage and read-length distributions.

Conclusions:

  • The integrated decoding approach significantly improves DNA data storage efficiency.
  • This method offers a practical solution to reduce reading costs in DNA storage systems.
  • Experimental validation confirms the effectiveness of the proposed techniques.