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Updated: Sep 11, 2025

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SynchDP: A correlation based sequence alignment algorithm for synchronizing longitudinal clinical data.

Seokhwan Seong1, Seunghwan Bae1, Jaeyeon Jang1

  • 1Kyungpook National University, School of Computer Science and Engineering, Buk-gu, Daegu, 41566, Daegu, Republic of Korea.

Computers in Biology and Medicine
|August 18, 2025
PubMed
Summary
This summary is machine-generated.

A new algorithm, SynchDP, aligns irregular clinical time-series data to track patient health progression and discover biomarkers. This method successfully synchronizes diverse patient data, improving disease progression analysis.

Keywords:
AlgorithmsEHRSequence alignmentSingle-cellSynchronizationTime-series

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Area of Science:

  • Computational Biology
  • Bioinformatics
  • Data Science

Background:

  • Clinical time-series data present challenges due to irregular intervals and varying lengths.
  • Comparing patient disease progression is difficult with asynchronous and irregularly sampled data.
  • This hinders accurate analysis of gene expression profiles and biomarker discovery.

Purpose of the Study:

  • To develop a novel algorithm for aligning and synchronizing multiple clinical time-series.
  • To enable de novo assembly of representative patterns from input sequences.
  • To facilitate robust comparison of patient disease trajectories.

Main Methods:

  • A correlation-based dynamic programming algorithm, SynchDP, was developed.
  • The algorithm handles irregular and asynchronous time-series data.
  • SynchDP was validated using synthetic data and COVID-19 patient severity levels.

Main Results:

  • SynchDP demonstrated superior alignment quality compared to existing methods on synthetic data.
  • The algorithm successfully synchronized COVID-19 patient data, identifying health deterioration and recovery patterns.
  • Biomarkers related to disease severity progression were effectively captured using single-cell transcriptome data.

Conclusions:

  • SynchDP provides a robust method for aligning complex clinical time-series.
  • The algorithm aids in understanding disease progression and identifying relevant biomarkers.
  • This approach has significant implications for personalized medicine and biomarker discovery.