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Study of the error correction capability of multiple sequence alignment algorithm (MAFFT) in DNA storage.

Ranze Xie1, Xiangzhen Zan1, Ling Chu1

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Summary
This summary is machine-generated.

Multiple sequence alignment (MSA) effectively corrects errors in DNA data storage. Simulations show MSA achieves high recovery rates below a 20% error threshold, offering a viable alternative to traditional error correction codes.

Keywords:
DNA storageError correctionMAFFTMultiple sequence alignment

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Area of Science:

  • Bioinformatics
  • Data Storage
  • Computational Biology

Background:

  • Synchronization errors, specifically insertions and deletions, pose significant challenges for reliable information retrieval in DNA data storage.
  • Traditional error correction codes (ECC) rely on adding redundancy, which can be inefficient for DNA storage systems.

Purpose of the Study:

  • To comprehensively evaluate the error correction capability of a typical multiple sequence alignment (MSA) algorithm, MAFFT, for DNA storage.
  • To understand the performance of MSA in relation to error rates and sequencing depth.

Main Methods:

  • Conducted a comprehensive simulation study using the MAFFT algorithm, a common MSA tool.
  • Analyzed the error correction performance under varying error percentages and sequencing depths.

Main Results:

  • MSA performance exhibits a phase transition around 20% error rate; below this, increasing sequencing depth improves recovery.
  • With sequencing depth up to 70, MSA achieves complete recovery in low error regimes and corrects up to 90% of errors in medium error regimes.
  • MSA demonstrates robustness to imperfect clustering and can be combined with ECC or other coding constraints.

Conclusions:

  • Multiple sequence alignment (MSA) presents a competitive strategy for error correction in DNA data storage, offering an alternative to traditional ECC.
  • Optimizing sequencing depth allows for a balance between cost and reading speed, making MSA a practical solution.
  • The robustness and combinability of MSA with other methods enhance its potential for future DNA storage applications.