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Binary genetic algorithm for optimal joinpoint detection: Application to cancer trend analysis.

Seongyoon Kim1, Sanghee Lee2, Jung-Il Choi1

  • 1School of Mathematics and Computing (Computational Science and Engineering), Yonsei University, Seoul, Korea.

Statistics in Medicine
|November 18, 2020
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Summary
This summary is machine-generated.

A new genetic algorithm-based joinpoint (GAJP) model efficiently detects multiple trend changepoints in data. This method improves computational speed over traditional grid search, making it suitable for large cancer incidence datasets.

Keywords:
SEERbinary genetic algorithmcancer incidencejoinpoint regression

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Area of Science:

  • Biostatistics
  • Computational Statistics
  • Epidemiology

Background:

  • Joinpoint regression models (JRM) identify trend changes using joinpoints (changepoints).
  • Existing grid search (GS)-based methods for joinpoint detection are computationally intensive, limiting the number of detectable joinpoints.
  • Accurate detection of multiple joinpoints is crucial for analyzing complex trends.

Purpose of the Study:

  • To develop a computationally efficient genetic algorithm-based joinpoint (GAJP) model for optimal joinpoint detection.
  • To overcome the limitations of existing grid search methods in terms of computational demand and the number of detectable joinpoints.
  • To evaluate the accuracy and performance of the GAJP model compared to GS-based methods.

Main Methods:

  • Developed a GAJP model embedding a binary genetic algorithm into the JRM.
  • Represented joinpoint combinations as binary chromosomes and used genetic operations to minimize fitness functions (Bayesian information criterion - BIC, BIC3).
  • Evaluated model performance through intensive simulations and comparison with GS-based methods using BIC, BIC3, and permutation tests.

Main Results:

  • The GAJP model demonstrated outstanding computational efficiency in detecting multiple joinpoints.
  • The proposed method is practically feasible for detecting multiple joinpoints without preassigning their number.
  • The GAJP model showed suitability for analyzing large cancer incidence datasets, as demonstrated with colorectal cancer data.

Conclusions:

  • The GAJP model offers a computationally efficient and feasible approach for detecting multiple joinpoints.
  • This method is easily extendable to analyze trends in large datasets, such as cancer incidence data.
  • The GAJP model provides a valuable tool for epidemiological trend analysis and public health research.