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Practical approach to determine sample size for building logistic prediction models using high-throughput data.

Publication ,  Journal Article
Son, D-S; Lee, D; Lee, K; Jung, S-H; Ahn, T; Lee, E; Sohn, I; Chung, J; Park, W; Huh, N; Lee, JW
Published in: J Biomed Inform
February 2015

An empirical method of sample size determination for building prediction models was proposed recently. Permutation method which is used in this procedure is a commonly used method to address the problem of overfitting during cross-validation while evaluating the performance of prediction models constructed from microarray data. But major drawback of such methods which include bootstrapping and full permutations is prohibitively high cost of computation required for calculating the sample size. In this paper, we propose that a single representative null distribution can be used instead of a full permutation by using both simulated and real data sets. During simulation, we have used a dataset with zero effect size and confirmed that the empirical type I error approaches to 0.05. Hence this method can be confidently applied to reduce overfitting problem during cross-validation. We have observed that pilot data set generated by random sampling from real data could be successfully used for sample size determination. We present our results using an experiment that was repeated for 300 times while producing results comparable to that of full permutation method. Since we eliminate full permutation, sample size estimation time is not a function of pilot data size. In our experiment we have observed that this process takes around 30min. With the increasing number of clinical studies, developing efficient sample size determination methods for building prediction models is critical. But empirical methods using bootstrap and permutation usually involve high computing costs. In this study, we propose a method that can reduce required computing time drastically by using representative null distribution of permutations. We use data from pilot experiments to apply this method for designing clinical studies efficiently for high throughput data.

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Published In

J Biomed Inform

DOI

EISSN

1532-0480

Publication Date

February 2015

Volume

53

Start / End Page

355 / 362

Location

United States

Related Subject Headings

  • Software
  • Sample Size
  • Research Design
  • Reproducibility of Results
  • Pilot Projects
  • Medical Informatics
  • Logistic Models
  • Humans
  • Gene Expression Profiling
  • Computer Simulation
 

Citation

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Son, D.-S., Lee, D., Lee, K., Jung, S.-H., Ahn, T., Lee, E., … Lee, J. W. (2015). Practical approach to determine sample size for building logistic prediction models using high-throughput data. J Biomed Inform, 53, 355–362. https://doi.org/10.1016/j.jbi.2014.12.010
Son, Dae-Soon, DongHyuk Lee, Kyusang Lee, Sin-Ho Jung, Taejin Ahn, Eunjin Lee, Insuk Sohn, et al. “Practical approach to determine sample size for building logistic prediction models using high-throughput data.J Biomed Inform 53 (February 2015): 355–62. https://doi.org/10.1016/j.jbi.2014.12.010.
Son D-S, Lee D, Lee K, Jung S-H, Ahn T, Lee E, et al. Practical approach to determine sample size for building logistic prediction models using high-throughput data. J Biomed Inform. 2015 Feb;53:355–62.
Son, Dae-Soon, et al. “Practical approach to determine sample size for building logistic prediction models using high-throughput data.J Biomed Inform, vol. 53, Feb. 2015, pp. 355–62. Pubmed, doi:10.1016/j.jbi.2014.12.010.
Son D-S, Lee D, Lee K, Jung S-H, Ahn T, Lee E, Sohn I, Chung J, Park W, Huh N, Lee JW. Practical approach to determine sample size for building logistic prediction models using high-throughput data. J Biomed Inform. 2015 Feb;53:355–362.
Journal cover image

Published In

J Biomed Inform

DOI

EISSN

1532-0480

Publication Date

February 2015

Volume

53

Start / End Page

355 / 362

Location

United States

Related Subject Headings

  • Software
  • Sample Size
  • Research Design
  • Reproducibility of Results
  • Pilot Projects
  • Medical Informatics
  • Logistic Models
  • Humans
  • Gene Expression Profiling
  • Computer Simulation